Practice Location

2011 MURPHY AVE
NASHVILLE, TN 37203-2047

Phone: (615) 301-1000

What does ELIZABETH OLDFIELD research?

Dr. Oldfield studies how different medications work against infections caused by fungi, parasites, and bacteria. She investigates both well-known drugs, like those used for tuberculosis, and newer compounds, including lipophilic bisphosphonates, to find effective treatments for serious conditions such as fungal infections, toxoplasmosis, and malaria. Her research aims to uncover new options that can help patients suffering from drug-resistant infections and improve patient outcomes.

Key findings

  • In her study on lipophilic bisphosphonates, 36 out of 75 compounds showed very effective antifungal activity, with two compounds requiring only 0.13 µg/mL to be effective, outperforming commonly used treatments.
  • Dr. Oldfield found that the tuberculosis drug SQ109 was effective against 16 types of fungi, achieving growth inhibition at concentrations as low as 4 µg/mL, showing promise for treating fungal infections.
  • In research on parasitic infections, MeSQ109 effectively killed parasites at a concentration of just 1.7 nanomoles, demonstrating minimal toxicity to human cells.

Frequently asked questions

Does Dr. Oldfield study fungal infections?
Yes, Dr. Oldfield's research includes developing new antifungal treatments and studying the effectiveness of various compounds against fungal infections.
What treatments has Dr. Oldfield researched?
She has researched a range of treatments, including lipophilic bisphosphonates for fungal infections and SQ109 for tuberculosis and malaria.
Is Dr. Oldfield's work relevant to patients with drug-resistant infections?
Absolutely, her studies specifically target drug-resistant infections to find new, effective treatments.
How does her research help patients with parasitic infections?
Her research aims to uncover new therapies that effectively treat difficult-to-manage parasitic infections, improving patient care.
What are lipophilic bisphosphonates?
These are a class of compounds that have shown effectiveness against fungal infections, particularly in cases where standard treatments fail.

Publications in plain English

Antifungal Activity of Lipophilic Bisphosphonates.

2026

ACS infectious diseases

Pandey AM, Zhou R, Singh D, Li F, He M +9 more

Plain English
This study explored the effectiveness of 75 new lipophilic bisphosphonates in fighting fungal infections. They found that 36 of these compounds were very effective, with some showing similar strength to known antifungal drugs: 2 had the lowest effective dose at just 0.13 µg/mL, much more potent than a commonly used treatment. This research is important because discovering new antifungal options can help address drug resistance in fungal infections. Who this helps: Patients with serious fungal infections, especially those resistant to standard treatments.

PubMed

Broad-Spectrum Activity and Mechanisms of Action of SQ109 on a Variety of Fungi.

2025

bioRxiv : the preprint server for biology

Malwal SR, Garcia-Rubio R, Kordalewska M, Patterson H, Zhang C +10 more

Plain English
Researchers studied the drug SQ109, usually used for tuberculosis, to see how well it works against 16 types of fungi. They found that SQ109 was effective against many fungi, with some showing promising results at a concentration of around 4 micrograms per milliliter. This matters because finding a new antifungal agent could help treat a variety of fungal infections, especially as some fungi have become resistant to existing treatments. Who this helps: This helps patients with fungal infections and healthcare providers looking for new treatment options.

PubMed

Activity of Carbazole, Aminoguanidine and Diamine Anti-infectives against.

2025

bioRxiv : the preprint server for biology

Singh D, Sleda MA, Pandey A, Malwal SR, Chen Y +6 more

Plain English
Researchers studied three anti-infective compounds—carbazole, aminoguanidine, and a series of diamine analogs—to see how effective they are against certain parasites, bacteria, and fungi. They found that these compounds inhibited growth at very low concentrations, with values around 2 µM for carbazole and aminoguanidine, and 2.3 µM for the diamine analogs. This matters because these findings suggest that these compounds could be used to develop new treatments for infections caused by various microbes. Who this helps: This helps patients suffering from infections that are resistant to current treatments.

PubMed

Anti-Parasitics with a Triple Threat: Targeting Parasite Enzymes, the Proton Motive Force, and Host Cell-Mediated Killing.

2025

ACS infectious diseases

Pandey AM, Malwal SR, Valladares-Delgado M, Labrador-Fagúndez L, Stella BG +9 more

Plain English
This study looked at the effectiveness of two experimental drugs, SQ109 and MeSQ109, against certain parasite forms that cause diseases like leishmaniasis. They found that MeSQ109 was particularly strong, effectively killing parasites inside cells at a concentration of just 1.7 nanomoles, and it was safe for the surrounding human cells, showing minimal toxicity. This discovery is important because it highlights a new way to treat parasitic infections that can be difficult to manage, potentially leading to better therapies. Who this helps: This helps patients suffering from parasitic infections and doctors treating these diseases.

PubMed

Broad-Spectrum Activity and Mechanisms of Action of SQ109 on a Variety of Fungi.

2025

ACS infectious diseases

Malwal SR, Garcia-Rubio R, Kordalewska M, Patterson H, Zhang C +10 more

Plain English
Researchers studied the effects of a tuberculosis drug called SQ109 on 16 different types of fungi. They found that SQ109 was effective against many of these fungi, with some requiring only about 4 micrograms per milliliter to stop their growth. This is important because it suggests that SQ109 might be a useful treatment for fungal infections, especially since it targets multiple pathways in the fungi's biology. Who this helps: This helps patients with fungal infections and doctors who treat them.

PubMed

Activity of Antibacterial/Antifungal Compounds against the Protozoan Parasite,.

2025

ACS infectious diseases

Singh D, Sleda MA, Malwal SR, Pandey AM, Chen Y +6 more

Plain English
This study looked at the effectiveness of certain antibacterial and antifungal drugs against a type of parasitic infection caused by protozoa. Researchers found that compounds like carbazole and phenylthiazole aminoguanidine worked well against parasites, with some showing effectiveness at concentrations as low as 2 micromolar. This is comparable to the tuberculosis drug SQ109, which also showed to reduce the viability of the parasite effectively. These findings are important because they reveal new potential treatments for parasitic diseases that currently have limited options. Who this helps: This helps patients suffering from parasitic infections.

PubMed

Who dies from venous thromboembolism after hospitalisation for other reasons in England?: a national retrospective cohort study.

2024

BMJ open

Healey F, Gower J, Roberts L, Arya R, Beresford M +4 more

Plain English
This study looked at deaths from a condition called venous thromboembolism (VTE) that can occur after people are hospitalized in England for other medical reasons between April 2017 and March 2020. It found that out of nearly 14,000 deaths linked to VTE, most happened after emergency hospital admissions and almost all occurred in the hospital or within 30 days of discharge. The findings suggest that efforts to prevent these deaths should focus more on emergency care and include those who have day procedures, rather than just planned admissions. Who this helps: This information benefits patients, healthcare providers, and hospital systems aiming to improve care and reduce mortality rates.

PubMed

The Tuberculosis Drug Candidate SQ109 and Its Analogs Have Multistage Activity against.

2024

ACS infectious diseases

Watson SJ, van der Watt ME, Theron A, Reader J, Tshabalala S +19 more

Plain English
Researchers studied a drug called SQ109 and its variations to see if they could be used to treat malaria, in addition to tuberculosis. They found that these drugs were effective against both the forms of malaria that infect humans and the forms that can be transmitted to mosquitoes, working well at concentrations between 100-300 nM, even against drug-resistant malaria strains. This discovery is important because it could lead to new treatments that combat malaria transmission and resistance. Who this helps: This helps patients suffering from malaria, especially in areas with drug-resistant strains.

PubMed

Lipophilic bisphosphonates reduced cyst burden and ameliorated hyperactivity of mice chronically infected with.

2024

mBio

Sleda MA, Pitafi ZF, Song W, Oldfield E, Moreno SNJ

Plain English
Researchers studied the effects of specific lipophilic bisphosphonates (BPH-1218, BPH-1236, and BPH-1238) on mice infected with chronic stages of toxoplasmosis, a disease caused by a parasite that can remain dormant in tissue cysts. They found that these compounds successfully reduced the number of cysts in the brains of infected mice and helped control the hyperactivity caused by the infection. This matters because current treatments are ineffective against the chronic stages of the disease and can cause allergic reactions in many patients. Who this helps: This helps patients with toxoplasmosis, particularly those experiencing chronic infections.

PubMed

Synthesis and Testing of Analogs of the Tuberculosis Drug Candidate SQ109 against Bacteria and Protozoa: Identification of Lead Compounds againstand Malaria Parasites.

2023

ACS infectious diseases

Stampolaki M, Malwal SR, Alvarez-Cabrera N, Gao Z, Moniruzzaman M +28 more

Plain English
Researchers studied a drug candidate called SQ109, which shows promise for treating tuberculosis, and created 18 new versions of it to see if they could also fight malaria and other bacteria. They found that while SQ109 was effective against some bacteria, two modified versions were 4 to 8 times more effective against a tough strain of bacteria and showed 4 to 10 times more effectiveness against malaria parasites with low toxicity to human cells. This is important because it could lead to new, safer treatments for malaria. Who this helps: This helps patients with malaria and tuberculosis, as well as doctors looking for effective treatments.

PubMed

Distinct Energy-Coupling Factor Transporter Subunits Enable Flavin Acquisition and Extracytosolic Trafficking for Extracellular Electron Transfer in Listeria monocytogenes.

2023

mBio

Rivera-Lugo R, Huang S, Lee F, Méheust R, Iavarone AT +4 more

Plain English
This study focused on the bacteria Listeria monocytogenes and how it transports vitamins, specifically a type of vitamin B called flavins, from the outside environment and within its cells. Researchers discovered that specific protein subunits help these bacteria import and export flavins in a controlled manner, revealing that the transport system is more intricate than initially thought. Understanding this process is important because flavins play a vital role in energy transfer and chemical reactions in bacteria, which can affect how these pathogens operate and how they might be targeted for treatment. Who this helps: This benefits researchers and doctors working on treatments for foodborne illnesses caused by Listeria monocytogenes.

PubMed

Investigation into the Mechanism of Action of the Tuberculosis Drug Candidate SQ109 and Its Metabolites and Analogues in Mycobacteria.

2023

Journal of medicinal chemistry

Malwal SR, Mazurek B, Ko J, Xie P, Barnes C +13 more

Plain English
This study looked at how the tuberculosis drug candidate SQ109 and its similar compounds work against the bacteria that cause the disease. Researchers found that when they added a specific molecule (undecaprenyl phosphate), the effectiveness of SQ109 increased by up to 20 times, which suggests that it targets important processes in the bacteria's growth. Understanding how SQ109 functions helps in improving treatments for tuberculosis, a disease that remains a major global health issue. Who this helps: This helps patients with tuberculosis and healthcare providers working to treat them.

PubMed

Phosphoantigens glue butyrophilin 3A1 and 2A1 to activate Vγ9Vδ2 T cells.

2023

Nature

Yuan L, Ma X, Yang Y, Qu Y, Li X +28 more

Plain English
This research looked at how certain molecules called phosphoantigens help activate a type of immune cell known as Vγ9Vδ2 T cells by connecting two proteins, BTN3A1 and BTN2A1. The study found that multiple phosphoantigens act as "molecular glues" that bind these proteins together in different ways, which is crucial for triggering T cell activation. Understanding this process is important because it can lead to new treatments for diseases like cancer and infections by designing drugs that can enhance or inhibit T cell activity. Who this helps: This helps patients with cancer and infections by improving immune therapies.

PubMed

Mycobacterial membrane protein Large 3-like-family proteins in bacteria, protozoa, fungi, plants, and animals: A bioinformatics and structural investigation.

2022

Proteins

Malwal SR, Oldfield E

Plain English
This study looked at a group of proteins that help transport lipids, which are fats important for cell function, in various living organisms such as bacteria, protozoa, fungi, plants, and animals. Researchers found that many of these organisms, including the bacteria responsible for tuberculosis and certain parasites, have similar protein structures that suggest they perform related roles in lipid transport. The findings emphasize that these transport proteins are crucial across different life forms, which could lead to better understanding of diseases linked to lipid transport. Who this helps: This helps researchers and doctors working on treating diseases related to lipid transport, including infections and metabolic disorders.

PubMed

In Vivo Efficacy of SQ109 against,spp. andand In Vitro Activity of SQ109 Metabolites.

2022

Biomedicines

Baek KH, Phan TN, Malwal SR, Lee H, Li ZH +3 more

Plain English
This study looked at the effectiveness of a drug called SQ109 in treating infections caused by certain protozoa in mice. The researchers found that 80% of the mice treated with SQ109 survived for 40 days after being infected, while all untreated mice died within 10 days. These findings are important because they support the potential use of SQ109 in combination with another drug for better treatment of these infections. Who this helps: This benefits doctors and researchers looking for effective treatments for protozoan infections.

PubMed

A Structural and Bioinformatics Investigation of a Fungal Squalene Synthase and Comparisons with Other Membrane Proteins.

2022

ACS omega

Malwal SR, Shang N, Liu W, Li X, Zhang L +3 more

Plain English
This research looked at a specific protein from fungi called squalene synthase (SQS), which could be important for developing new antifungal drugs due to rising drug resistance. The study found that the fungal SQS has a unique structure, including a special helix that is not found in similar proteins from humans or other organisms, which may play a role in how these proteins interact with each other. This is significant because targeting this unique feature could lead to the creation of more effective antifungal treatments. Who this helps: This helps patients suffering from fungal infections and doctors treating those infections.

PubMed

The Heptaprenyl Diphosphate Synthase (Coq1) Is the Target of a Lipophilic Bisphosphonate That Protects Mice against Toxoplasma gondii Infection.

2022

mBio

Sleda MA, Li ZH, Behera R, Baierna B, Li C +5 more

Plain English
This study examined an enzyme called Coq1 in a parasite known as Toxoplasma gondii, which can cause serious diseases, especially in people with weakened immune systems. Researchers found that a chemical called BPH-1218 can effectively stop the growth of this parasite, even at very low doses, and it also protected mice from a deadly infection. This is important because it shows potential for developing safer and more effective treatments for toxoplasmosis, an infection that affects millions. Who this helps: Patients at risk of toxoplasmosis, especially those who are immunocompromised or pregnant.

PubMed

A polymeric approach toward resistance-resistant antimicrobial agent with dual-selective mechanisms of action.

2021

Science advances

Bai S, Wang J, Yang K, Zhou C, Xu Y +14 more

Plain English
This research focused on creating a new type of antibiotic that can fight resistant bacteria without the bacteria developing resistance itself. The new polymer showed great results, effectively killing a range of harmful bacteria, including those that are resistant to most antibiotics, while not causing harm to human cells. Specifically, it completely cleared infections in mice, indicating its strong potential for treating severe bacterial infections. Who this helps: This benefits patients with severe bacterial infections, especially those with antibiotic-resistant strains.

PubMed

Immuno-antibiotics: targeting microbial metabolic pathways sensed by unconventional T cells.

2021

Immunotherapy advances

Eberl M, Oldfield E, Herrmann T

Plain English
This study looks at how certain immune cells in our bodies recognize specific substances produced by bacteria that humans do not make. The researchers found that by shutting down these bacterial pathways, it’s possible to not only kill the bacteria but also boost the body's immune response. This is important because these findings pave the way for new antibiotics that can both fight infection and help the immune system recognize and respond to pathogens more effectively. Who this helps: This benefits patients battling infections, especially those with antibiotic-resistant bacteria.

PubMed

Structure,Detection, and Antibacterial Activity of Metabolites of SQ109, an Anti-Infective Drug Candidate.

2021

ACS infectious diseases

Malwal SR, Zimmerman MD, Alvarez N, Sarathy JP, Dartois V +2 more

Plain English
This study focused on a drug called SQ109, which is being developed to treat tuberculosis (TB). Researchers looked at how the drug is processed by the body and whether its breakdown products, or metabolites, help in fighting TB. They found that while SQ109 builds up to effective levels in the lungs, its metabolites did not show antibacterial effects against bacteria related to TB. This means that the effectiveness of SQ109 in treating TB comes from the drug itself rather than its breakdown products. Who this helps: This research helps patients with tuberculosis and the doctors treating them.

PubMed

Editor's Note: Relates to: 'Immuno-antibiotics: targeting microbial metabolic pathways sensed by unconventional T cells'.

2021

Immunotherapy advances

Eberl M, Oldfield E, Herrmann T

PubMed

SQ109 inhibits proliferation of Leishmania donovani by disruption of intracellular Cahomeostasis, collapsing the mitochondrial electrochemical potential (ΔΨ) and affecting acidocalcisomes.

2020

Parasitology research

Gil Z, Martinez-Sotillo N, Pinto-Martinez A, Mejias F, Martinez JC +3 more

Plain English
This study tested a drug called SQ109, originally intended for tuberculosis, to see how it affects the parasite responsible for visceral leishmaniasis (Leishmania donovani). The researchers found that SQ109 can kill this parasite with a very low dose of about 7.17 nanomoles, which is even more effective than its action on related parasites. This is important because visceral leishmaniasis is a severe and often deadly disease, and the high selectivity of SQ109 means it could target the parasite without harming healthy cells. Who this helps: This research benefits patients suffering from visceral leishmaniasis and healthcare providers looking for effective treatments.

PubMed

COVID-19 and Other Pandemics: How Might They Be Prevented?

2020

ACS infectious diseases

Oldfield E, Malwal SR

Plain English
This study looked at how to better protect ourselves from respiratory infections like COVID-19 and other pandemics. It found that using filtered eye masks can help prevent the virus from entering through the eyes, and that new types of respirators with valves could be more effective at blocking viruses compared to regular face masks. This is important because effective protection can reduce the spread of infections and save lives. Who this helps: This helps patients, health workers, and anyone looking to reduce their risk of respiratory infections.

PubMed

Discovery of Prenyltransferase Inhibitors withandAntibacterial Activity.

2020

ACS infectious diseases

Song J, Malwal SR, Baig N, Schurig-Briccio LA, Gao Z +8 more

Plain English
This study focused on finding new compounds that can block certain enzymes in bacteria that are essential for building their cell walls. The researchers tested 750 different compounds and identified 17 that successfully inhibited these enzymes, with one compound, called redoxal, showing particularly strong effects against bacteria. Importantly, redoxal reduced bacterial growth three times more effectively than the commonly used antibiotic ampicillin. Who this helps: This research benefits patients with bacterial infections by potentially leading to the development of more effective antibiotics.

PubMed

Discovery of Lipophilic Bisphosphonates That Target Bacterial Cell Wall and Quinone Biosynthesis.

2019

Journal of medicinal chemistry

Malwal SR, Chen L, Hicks H, Qu F, Liu W +11 more

Plain English
Researchers studied a group of compounds called alkyl-substituted bisphosphonates to see how effective they were against different bacteria, including Bacillus anthracis and Staphylococcus aureus. They found that these compounds successfully inhibited the growth of these bacteria at very low concentrations, specifically needing just 0.40 µg/mL for Bacillus anthracis and 1.0 µg/mL for Bacillus subtilis. This matters because it shows these bisphosphonates can target specific bacterial functions without significantly affecting human cells, which could lead to new treatments for bacterial infections, including those caused by hard-to-treat bacteria like Clostridioides difficile. Who this helps: This benefits patients with bacterial infections, especially those resistant to current treatments.

PubMed

Complex structures of MoeN5 with substrate analogues suggest sequential catalytic mechanism.

2019

Biochemical and biophysical research communications

Zhang L, Ko TP, Malwal SR, Liu W, Zhou S +4 more

Plain English
This study looked at how the enzyme MoeN5 helps create a part of the antibiotic moenomycin A. Researchers discovered that two modified versions of a sugar-linked compound, instead of binding in the expected site (S2), actually preferred to attach to the primary site (S1) on the enzyme. This finding suggests that MoeN5 operates in steps, using a specific process to create the antibiotic, which is important for developing new strategies to produce effective antibiotics. Who this helps: This helps patients by aiding the development of better antibiotics.

PubMed

A Structural Change in Butyrophilin upon Phosphoantigen Binding Underlies Phosphoantigen-Mediated Vγ9Vδ2 T Cell Activation.

2019

Immunity

Yang Y, Li L, Yuan L, Zhou X, Duan J +18 more

Plain English
This study looked at how a protein called butyrophilin helps activate a type of immune cell known as Vγ9Vδ2 T cells, which are important for fighting infections and cancer. The researchers found that when a specific molecule called HMBPP binds to butyrophilin, it significantly strengthens the connection between T cells and target cells—doubling the binding force during interactions. This discovery is important because it enhances our understanding of how these immune cells are activated, which can lead to better treatments for various diseases. Who this helps: This helps patients with infections or cancers that require stronger immune responses.

PubMed

Aspergillus flavus squalene synthase as an antifungal target: Expression, activity, and inhibition.

2019

Biochemical and biophysical research communications

Song J, Shang N, Baig N, Yao J, Shin C +6 more

Plain English
This study examined a protein called squalene synthase (SQS) from the fungus Aspergillus flavus, which causes a serious disease known as invasive aspergillosis, especially in patients with weakened immune systems. Researchers found that a compound called celastrol effectively blocks SQS with an inhibitory concentration of 830 nanomolar, suggesting it could be used to treat infections from this fungus. This discovery is important because it may lead to new antifungal treatments that are less toxic and more effective against resistant strains of the fungus. Who this helps: Patients with invasive aspergillosis and their doctors.

PubMed

Mycobacterium tuberculosis releases an antacid that remodels phagosomes.

2019

Nature chemical biology

Buter J, Cheng TY, Ghanem M, Grootemaat AE, Raman S +25 more

Plain English
Researchers studied a substance produced by Mycobacterium tuberculosis (Mtb), the bacteria responsible for tuberculosis, which can disrupt immune cells trying to destroy it. They found that this substance, called 1-TbAd, neutralizes acidic environments inside the immune cells, allowing Mtb to survive and thrive; it is commonly found in Mtb strains from patients. This discovery is important because it reveals how Mtb protects itself from the immune response, which could help develop better treatments. Who this helps: This helps doctors and researchers working to create more effective therapies for tuberculosis patients.

PubMed

Farnesyl Pyrophosphate Synthase as a Target for Drug Development: Discovery of Natural-Product-Derived Inhibitors and Their Activity in Pancreatic Cancer Cells.

2019

Journal of medicinal chemistry

Han S, Li X, Xia Y, Yu Z, Cai N +4 more

Plain English
This study focused on a protein called farnesyl pyrophosphate synthase (FPPS), which plays a role in certain cancers and bone diseases. Researchers found that a natural compound from rosemary, called carnosic acid, was more effective than a common cancer drug in stopping the growth of pancreatic cancer cells. Their work shows that carnosic acid works by disrupting a specific process the cancer cells rely on, which could lead to new treatments for soft tissue cancers. Who this helps: This helps patients with pancreatic cancer and other soft tissue cancers.

PubMed

"Head-to-Middle" and "Head-to-Tail" cis-Prenyl Transferases: Structure of Isosesquilavandulyl Diphosphate Synthase.

2018

Angewandte Chemie (International ed. in English)

Gao J, Ko TP, Chen L, Malwal SR, Zhang J +10 more

Plain English
This research looks at a specific enzyme called isosesquilavandulyl diphosphate synthase, which plays a role in making certain antibiotics known as merochlorins. The scientists discovered its structure using X-ray crystallography and found that it has a unique arrangement that differs from other similar enzymes. This new understanding of how the enzyme works could lead to the development of improved antibiotics. Who this helps: This benefits researchers and pharmaceutical companies working on new antibiotic treatments.

PubMed

Remarkable similarity in Plasmodium falciparum and Plasmodium vivax geranylgeranyl diphosphate synthase dynamics and its implication for antimalarial drug design.

2018

Chemical biology & drug design

Venkatramani A, Gravina Ricci C, Oldfield E, McCammon JA

Plain English
This study focused on two types of malaria-causing parasites, Plasmodium falciparum and Plasmodium vivax, specifically looking at an enzyme called geranylgeranyl diphosphate synthase (GGPPS) that is important for the parasites' survival. Researchers found that both enzymes are very similar in how they operate, allowing potential drugs targeting one to work on the other as well. By creating models of the parasite's enzyme structures, they can now screen for new medications to fight malaria more effectively. Who this helps: This benefits patients suffering from malaria by potentially leading to better treatment options.

PubMed

Alkynyl-containing phenylthiazoles: Systemically active antibacterial agents effective against methicillin-resistant Staphylococcus aureus (MRSA).

2018

European journal of medicinal chemistry

Elsebaei MM, Mohammad H, Abouf M, Abutaleb NS, Hegazy YA +7 more

Plain English
The research focused on developing new antibacterial agents called phenylthiazoles to effectively treat methicillin-resistant Staphylococcus aureus (MRSA), a tough bacterial infection. The study found that a specific compound, identified as compound 9, effectively killed MRSA bacteria at very low doses, showing a half-life of about 4.5 hours in the body, and was comparable in effectiveness to the standard treatment, vancomycin, but required a lower dose to achieve results. This is significant because it could lead to more effective treatments for patients with serious MRSA infections, particularly those that are resistant to other antibiotics. Who this helps: Patients with MRSA infections.

PubMed

Bisphosphonate-Generated ATP-Analogs Inhibit Cell Signaling Pathways.

2018

Journal of the American Chemical Society

Malwal SR, O'Dowd B, Feng X, Turhanen P, Shin C +8 more

Plain English
This study looked at how certain drugs called bisphosphonates, which are used to treat bone diseases like osteoporosis and some types of cancer, work at a cellular level. The researchers found that a specific version of these drugs can effectively block certain enzymes (kinases) involved in cell signaling, which are important for cell growth and survival. They discovered that these drugs create analogs of ATP (a molecule that helps cells produce energy), leading to a strong interaction that inhibits selected kinases—this could help develop better treatments for bone issues and cancer. Who this helps: This research benefits patients with osteoporosis, Paget's disease, and cancer.

PubMed

Structure-activity relationship investigation of coumarin-chalcone hybrids with diverse side-chains as acetylcholinesterase and butyrylcholinesterase inhibitors.

2018

Molecular diversity

Kang L, Gao XH, Liu HR, Men X, Wu HN +3 more

Plain English
The researchers studied 36 new compounds made from coumarin and chalcone to see how well they could block two enzymes linked to Alzheimer's disease: acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). They found that some compounds, especially one called 5e, effectively inhibited AChE with a strong selectivity ratio of 27.4 over BChE, meaning it worked better on one enzyme than the other. This is important because it suggests that these compounds could lead to better treatments for Alzheimer's by targeting AChE specifically. Who this helps: Patients with Alzheimer's disease.

PubMed

The Mevalonate Pathway Is a Druggable Target for Vaccine Adjuvant Discovery.

2018

Cell

Xia Y, Xie Y, Yu Z, Xiao H, Jiang G +18 more

Plain English
This study looked at a biological pathway called the mevalonate pathway to see if it could help improve vaccines. Researchers found that existing drugs, like statins, can boost vaccine effectiveness in mice and monkeys by enhancing the immune response, with one example being a significant increase in T-cell activation. This is important because it suggests new ways to make vaccines and cancer treatments work better together. Who this helps: This benefits patients seeking more effective vaccines and cancer treatments.

PubMed

Catalytic Role of Conserved Asparagine, Glutamine, Serine, and Tyrosine Residues in Isoprenoid Biosynthesis Enzymes.

2018

ACS catalysis

Malwal SR, Gao J, Hu X, Yang Y, Liu W +10 more

Plain English
This study investigated how certain building blocks of proteins, specifically asparagine, glutamine, serine, and tyrosine, help enzymes involved in producing isoprenoids, which are important compounds in many biological processes. Researchers looked at the structure of an enzyme called cyclolavandulyl diphosphate synthase and found that these amino acids play a crucial role in helping the enzyme function effectively. They discovered that these amino acids can assist in removing protons from molecules, significantly impacting how these enzymes work in producing important compounds. Who this helps: This research helps scientists and pharmaceutical developers improve processes for creating essential compounds used in medicine and other industries.

PubMed

Phenylthiazole Antibacterial Agents Targeting Cell Wall Synthesis Exhibit Potent Activity in Vitro and in Vivo against Vancomycin-Resistant Enterococci.

2017

Journal of medicinal chemistry

Mohammad H, Younis W, Chen L, Peters CE, Pogliano J +7 more

Plain English
This study focused on three new antibacterial compounds that target certain bacteria resistant to traditional antibiotics, specifically vancomycin-resistant enterococci (VRE). The researchers found that these compounds effectively stopped the growth of VRE at very low concentrations (as low as 0.5 micrograms per milliliter) and worked quickly to kill the bacteria. Using an animal model, they showed that two of the compounds reduced the infection burden in worms, suggesting they could be powerful new treatments against drug-resistant infections. Who this helps: This research benefits patients suffering from infections caused by antibiotic-resistant bacteria.

PubMed

Spectroscopic and Computational Investigations of Ligand Binding to IspH: Discovery of Non-diphosphate Inhibitors.

2017

Chembiochem : a European journal of chemical biology

O'Dowd B, Williams S, Wang H, No JH, Rao G +4 more

Plain English
This study looked at how certain small molecules interact with a key enzyme called IspH, which is important for producing compounds that help in fighting infections. Researchers found that these small molecules can attach to the enzyme’s iron-containing cluster, with one promising compound, a type of barbituric acid, effectively inhibiting IspH activity at a concentration of around 500 nanomolar against a common infection-causing bacteria, Pseudomonas aeruginosa. Understanding how to block this enzyme may lead to new treatments for bacterial infections, making it a significant step in drug development. Who this helps: This benefits patients with infections, particularly those caused by antibiotic-resistant bacteria.

PubMed

Head-to-Head Prenyl Synthases in Pathogenic Bacteria.

2017

Chembiochem : a European journal of chemical biology

Schwalen CJ, Feng X, Liu W, O-Dowd B, Ko TP +4 more

Plain English
The study looked at enzymes called prenyl synthases in three types of disease-causing bacteria: Neisseria meningitidis, Neisseria gonorrhoeae, and Enterococcus hirae. Researchers found that the Enteococcus hirae enzyme produced a compound called dehydrosqualene, while the enzymes from the Neisseria species only produced a different compound called presqualene diphosphate (PSPP). These findings indicate that these bacteria have similar but different types of enzymes, which could play a role in how they cause disease. Who this helps: This helps researchers and healthcare professionals understand bacterial functions and could lead to better treatments for infections.

PubMed

Anticancer Activity of Polyoxometalate-Bisphosphonate Complexes: Synthesis, Characterization, In Vitro and In Vivo Results.

2017

Inorganic chemistry

Boulmier A, Feng X, Oms O, Mialane P, Rivière E +6 more

Plain English
This study looked at new chemical compounds made from polyoxometalates and bisphosphonates to see how well they fight certain types of cancer. Researchers found that these compounds were effective in killing human lung cancer cells, showing that one compound reduced tumor size in mice by about five times more than the original bisphosphonate, zoledronate, when given the same dose. These findings are important because they offer new ways to treat aggressive cancers by targeting specific growth pathways. Who this helps: This helps cancer patients, particularly those with lung cancer and sarcoma.

PubMed

Pulsed Electron Paramagnetic Resonance Insights into the Ligand Environment of Copper in Drosophila Lysyl Oxidase.

2017

Biochemistry

Rao G, Bansal S, Law WX, O'Dowd B, Dikanov SA +1 more

Plain English
This study focused on a protein called lysyl oxidase (LOX) that is important for building strong connective tissue and is linked to cancer and fibrosis. Researchers examined a version of this protein from fruit flies (Drosophila) to understand how copper interacts with it. They discovered that at different pH levels, the way copper binds to a specific part of the protein changes, which could influence how this protein functions in the body. Understanding these interactions is crucial because LOX is a target for developing new cancer treatments. Who this helps: Patients with cancer and doctors developing targeted therapies.

PubMed

Combining Vγ9Vδ2 T Cells with a Lipophilic Bisphosphonate Efficiently Kills Activated Hepatic Stellate Cells.

2017

Frontiers in immunology

Zhou X, Gu Y, Xiao H, Kang N, Xie Y +6 more

Plain English
This study looked at how a type of immune cell called Vγ9Vδ2 T cells can kill liver cells that contribute to serious liver diseases, such as fibrosis and cancer. The researchers found that these T cells are less active in people with liver cirrhosis but can effectively kill harmful liver cells when combined with a drug called BPH-1236; in experiments, this combination significantly boosted the T cells' ability to destroy these liver cells. This matters because it suggests a new way to treat severe liver conditions through immunotherapy, potentially stopping disease progression. Who this helps: This helps patients with liver diseases, especially those suffering from cirrhosis and cancer.

PubMed

Structure and Function of Four Classes of the 4Fe-4S Protein, IspH.

2016

Biochemistry

Rao G, Oldfield E

Plain English
This study looked at a vital enzyme called IspH, which plays a role in creating certain essential compounds and is a target for drugs and herbicides. Researchers discovered that there are four types of this enzyme, each adapted to different living conditions – for example, some are found in bacteria that thrive with little oxygen, while others are in plants and parasites. They found that changes in specific parts of these enzymes affect their stability and how well they work, which is important for understanding how various organisms survive in challenging environments. Who this helps: This helps scientists and doctors working on treatments for infections and diseases caused by bacteria and parasites.

PubMed

Structure, Function, and Inhibition of Staphylococcus aureus Heptaprenyl Diphosphate Synthase.

2016

ChemMedChem

Desai J, Liu YL, Wei H, Liu W, Ko TP +2 more

Plain English
This study looked at a specific enzyme in the Staphylococcus aureus bacteria that plays a critical role in producing a substance needed for energy transport in many bacteria. Researchers discovered the structure of this enzyme and found that it can be effectively inhibited by certain compounds, particularly ones related to bisphosphonates, with the best inhibitors working at levels around 200 nanomoles. Understanding this enzyme is important because it could lead to new antibiotics that target S. aureus, which is known for causing serious infections. Who this helps: This helps patients at risk of S. aureus infections and doctors seeking new treatment options.

PubMed

Inhibition of Leishmania mexicana Growth by the Tuberculosis Drug SQ109.

2016

Antimicrobial agents and chemotherapy

García-García V, Oldfield E, Benaim G

Plain English
Researchers studied how the tuberculosis drug SQ109 affects the Leishmania mexicana parasite, which causes a disease called leishmaniasis. They found that SQ109 effectively inhibited the growth of the parasite in laboratory tests, with a strong effect at very low concentrations (about 11 nanomoles per liter). This is important because it suggests that SQ109 could be a promising new treatment for leishmaniasis, a disease that currently has limited treatment options. Who this helps: This helps patients suffering from leishmaniasis.

PubMed

A Highly Efficient Single-Chain Metal-Organic Nanoparticle Catalyst for Alkyne-Azide "Click" Reactions in Water and in Cells.

2016

Journal of the American Chemical Society

Bai Y, Feng X, Xing H, Xu Y, Kim BK +6 more

Plain English
This study explored how copper-based nanoparticles can be created and used as catalysts in a specific type of chemical reaction known as "click chemistry," which combines two molecules to form a new compound. The researchers found that these nanoparticles can work effectively even in very small amounts—just a few parts per million—while being safe for use in water and inside living cells. This is important because it provides a greener way to create complex molecules that could be used in medicine or materials science. Who this helps: This benefits scientists and researchers working in drug development and material synthesis.

PubMed

Dynamic Structure and Inhibition of a Malaria Drug Target: Geranylgeranyl Diphosphate Synthase.

2016

Biochemistry

G Ricci C, Liu YL, Zhang Y, Wang Y, Zhu W +2 more

Plain English
This study looked at a key enzyme, geranylgeranyl diphosphate synthase (GGPPS), found in the malaria parasite that could be a target for new drugs. Researchers discovered several compounds that can hinder this enzyme's activity and used simulations to understand how these inhibitors work. Their findings are important because they provide a detailed understanding of how to interfere with GGPPS, which could lead to the development of new antimalarial medications. Who this helps: This helps patients suffering from malaria by potentially leading to better treatments.

PubMed

Isoprenoid Biosynthesis Inhibitors Targeting Bacterial Cell Growth.

2016

ChemMedChem

Desai J, Wang Y, Wang K, Malwal SR, Oldfield E

Plain English
This study explored new compounds that can inhibit certain enzymes involved in bacterial growth, specifically focusing on Gram-negative and Gram-positive bacteria. The researchers found that compounds called bisphosphonates effectively blocked the growth of harmful Gram-negative bacteria like E. coli at very low concentrations (around 1-4 micrograms per milliliter), while other compounds inhibited different enzymes and affected Gram-positive bacteria at slightly higher levels (2-6 micrograms per milliliter). These findings are important because they identify potential new treatments for antibiotic-resistant bacterial infections. Who this helps: This helps patients suffering from infections caused by antibiotic-resistant bacteria.

PubMed

Bacterial Cell Growth Inhibitors Targeting Undecaprenyl Diphosphate Synthase and Undecaprenyl Diphosphate Phosphatase.

2016

ChemMedChem

Wang Y, Desai J, Zhang Y, Malwal SR, Shin CJ +5 more

Plain English
This study looked at how certain chemical compounds affect the growth of two bacteria, Staphylococcus aureus and Bacillus subtilis, which are important in infections. One of the strongest compounds tested, 5-fluoro-2-(3-(octyloxy)benzamido)benzoic acid, was found to significantly enhance the effectiveness of seven antibiotics, reducing bacterial growth to about 0.15 micrograms per milliliter, while having little effect when combined with other types of antibiotics. This research is important because it could lead to new treatments that better fight harmful bacteria by targeting key processes in their cell wall construction. Who this helps: This helps patients with bacterial infections, particularly those caused by antibiotic-resistant strains.

PubMed

Frequent Co-Authors

Satish R Malwal Rey-Ting Guo Yonghui Zhang Xinxin Feng Weidong Liu Chun-Chi Chen Akanksha M Pandey Ruijie Zhou Davinder Singh Silvia N J Moreno

Physician data sourced from the NPPES NPI Registry . Publication data from PubMed . Plain-English summaries generated by AI. Not medical advice.