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Schiffer Lab
Biochemistry and Molecular Biotechnology
Research
Research
Overview: Drug Resistance
Molecular Basis for Resistance
Substrate Envelope
Inhibitor Design
Integrated Strategies to Elucidate Molecular Recognition
Introducing Sequence Diversity: APOBEC3s
Scientific Leadership
Scientific Leadership
About Celia Schiffer
Institute for Drug Resistance
Structure Based Drug Design Core
Cryo EM Core Facility
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Publications
Dissertations
Journal Publications
Publications
Dissertations
Journal Publications
Publications
Total:
50
results
Elucidating the Substrate Envelope of Enterovirus 68-3C Protease: Structural Basis of Specificity and Potential Resistance
septiembre 28, 2024
Author(s):
Vincent N Azzolino,Ala M Shaqra,Akbar Ali,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Viruses
Enterovirus-D68 (EV68) has emerged as a global health concern over the last decade with severe symptomatic infections resulting in long-lasting neurological deficits and death. Unfortunately, there ar...
FcRn-enhancing mutations lead to increased and prolonged levels of the HIV CCR5-blocking monoclonal antibody leronlimab in the fetuses and newborns of pregnant rhesus macaques
septiembre 26, 2024
Author(s):
Joanna Zikos,Gabriela M Webb,Helen L Wu,Jason S Reed,Jennifer Watanabe,Jodie L Usachenko,Ala M Shaqra,Celia A Schiffer,Koen K A Van Rompay,Jonah B Sacha,Diogo M Magnani
Source:
mAbs
Prenatal administration of monoclonal antibodies (mAbs) is a strategy that could be exploited to prevent viral infections during pregnancy and early life. To reach protective levels in fetuses, mAbs m...
Increasing intracellular dNTP levels improves prime editing efficiency
septiembre 25, 2024
Author(s):
Pengpeng Liu,Karthikeyan Ponnienselvan,Thomas Nyalile,Sarah Oikemus,Anya T Joynt,Sukanya Iyer,Karen Kelly,Dongsheng Guo,Pyae P Kyawe,Emma Vanderleeden,Sambra D Redick,Lei Huang,Zexiang Chen,Jeong Min ...
Source:
Nature biotechnology
In primary cell types, intracellular deoxynucleotide triphosphate (dNTP) levels are tightly regulated in a cell cycle-dependent manner. We report that prime editing efficiency is increased by mutation...
Next generation APOBEC3 inhibitors: Optimally designed for potency and nuclease stability
septiembre 16, 2024
Author(s):
Adam K Hedger,Wazo Myint,Jeong Min Lee,Diego Suchenski-Loustaunau,Vanivilasini Balachandran,Ala M Shaqra,Nese Kurt-Yilmaz,Jonathan K Watts,Hiroshi Matsuo,Celia A Schiffer
Source:
bioRxiv : the preprint server for biology
APOBEC3 (or A3) enzymes have emerged as potential therapeutic targets due to their role in introducing heterogeneity in viruses and cancer, often leading to drug resistance. Inhibiting these enzymes h...
Contributions of Hyperactive Mutations in Mpro from SARS-CoV-2 to Drug Resistance
marzo 12, 2024
Author(s):
Julia M Flynn,Sarah N Zvornicanin,Tenzin Tsepal,Ala M Shaqra,Nese Kurt Yilmaz,Weiping Jia,Stephanie Moquin,Dustin Dovala,Celia A Schiffer,Daniel N A Bolon
Source:
ACS infectious diseases
The appearance and spread of mutations that cause drug resistance in rapidly evolving diseases, including infections by the SARS-CoV-2 virus, are major concerns for human health. Many drugs target enz...
Direct delivery of stabilized Cas-embedded base editors achieves efficient and accurate editing of clinically relevant targets
febrero 19, 2024
Author(s):
Jeong Min Lee,Jing Zeng,Pengpeng Liu,My Anh Nguyen,Diego Suchenski Loustaunau,Daniel E Bauer,Nese Kurt Yilmaz,Scot A Wolfe,Celia A Schiffer
Source:
bioRxiv : the preprint server for biology
Over the last 5 years, cytosine base editors (CBEs) have emerged as a promising therapeutic tool for specific editing of single nucleotide variants and disrupting specific genes associated with diseas...
Open science discovery of potent noncovalent SARS-CoV-2 main protease inhibitors
noviembre 09, 2023
Author(s):
Melissa L Boby,Daren Fearon,Matteo Ferla,Mihajlo Filep,Lizbé Koekemoer,Matthew C Robinson,COVID Moonshot Consortium‡,John D Chodera,Alpha A Lee,Nir London,Annette von Delft,Frank von Delft,Hagit Achdo...
Source:
Science (New York, N.Y.)
We report the results of the COVID Moonshot, a fully open-science, crowdsourced, and structure-enabled drug discovery campaign targeting the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2...
Addressing the dNTP bottleneck restricting prime editing activity
octubre 31, 2023
Author(s):
Karthikeyan Ponnienselvan,Pengpeng Liu,Thomas Nyalile,Sarah Oikemus,Anya T Joynt,Karen Kelly,Dongsheng Guo,Zexiang Chen,Jeong Min Lee,Celia A Schiffer,Charles P Emerson,Nathan D Lawson,Jonathan K Watt...
Source:
bioRxiv : the preprint server for biology
Prime editing efficiency is modest in cells that are quiescent or slowly proliferating where intracellular dNTP levels are tightly regulated. MMLV-reverse transcriptase - the prime editor polymerase s...
FruitFire: a luciferase based on a fruit fly metabolic enzyme
julio 10, 2023
Author(s):
Spencer T Adams,Jacqueto Zephyr,Markus F Bohn,Celia A Schiffer,Stephen C Miller
Source:
bioRxiv : the preprint server for biology
Firefly luciferase is homologous to fatty acyl-CoA synthetases from insects that are not bioluminescent. Here, we determined the crystal structure of the fruit fly fatty acyl-CoA synthetase CG6178 to ...
Systematic Analyses of the Resistance Potential of Drugs Targeting SARS-CoV-2 Main Protease
junio 30, 2023
Author(s):
Julia M Flynn,Qiu Yu J Huang,Sarah N Zvornicanin,Gila Schneider-Nachum,Ala M Shaqra,Nese Kurt Yilmaz,Stephanie A Moquin,Dustin Dovala,Celia A Schiffer,Daniel N A Bolon
Source:
ACS infectious diseases
Drugs that target the main protease (M^(pro)) of SARS-CoV-2 are effective therapeutics that have entered clinical use. Wide-scale use of these drugs will apply selection pressure for the evolution of ...
HIV-1 protease inhibitors with a P1 phosphonate modification maintain potency against drug-resistant variants by increased interactions with flap residues
mayo 27, 2023
Author(s):
Gordon J Lockbaum,Linah N Rusere,Mina Henes,Klajdi Kosovrasti,Desaboini Nageswara Rao,Ean Spielvogel,Sook-Kyung Lee,Ellen A Nalivaika,Ronald Swanstrom,Nese Kurt Yilmaz,Celia A Schiffer,Akbar Ali
Source:
European journal of medicinal chemistry
Protease inhibitors are the most potent antivirals against HIV-1, but they still lose efficacy against resistant variants. Improving the resistance profile is key to developing more robust inhibitors,...
Crystal Structures of Inhibitor-Bound Main Protease from Delta- and Gamma-Coronaviruses
marzo 30, 2023
Author(s):
Sarah N Zvornicanin,Ala M Shaqra,Qiuyu J Huang,Elizabeth Ornelas,Mallika Moghe,Mark Knapp,Stephanie Moquin,Dustin Dovala,Celia A Schiffer,Nese Kurt Yilmaz
Source:
Viruses
With the spread of SARS-CoV-2 throughout the globe causing the COVID-19 pandemic, the threat of zoonotic transmissions of coronaviruses (CoV) has become even more evident. As human infections have bee...
Selection of HIV-1 for resistance to fifth-generation protease inhibitors reveals two independent pathways to high-level resistance
marzo 15, 2023
Author(s):
Ean Spielvogel,Sook-Kyung Lee,Shuntai Zhou,Gordon J Lockbaum,Mina Henes,Amy Sondgeroth,Klajdi Kosovrasti,Ellen A Nalivaika,Akbar Ali,Nese Kurt Yilmaz,Celia A Schiffer,Ronald Swanstrom
Source:
eLife
Darunavir (DRV) is exceptional among potent HIV-1 protease inhibitors (PIs) in high drug concentrations that are achieved in vivo. Little is known about the de novo resistance pathway for DRV. We sele...
Non-canonical pattern recognition of a pathogen-derived metabolite by a nuclear hormone receptor identifies virulent bacteria in C. elegans
febrero 22, 2023
Author(s):
Nicholas D Peterson,Samantha Y Tse,Qiuyu Judy Huang,Khursheed A Wani,Celia A Schiffer,Read Pukkila-Worley
Source:
Immunity
Distinguishing infectious pathogens from harmless microorganisms is essential for animal health. The mechanisms used to identify infectious microbes are not fully understood, particularly in metazoan ...
Allosteric quinoxaline-based inhibitors of the flavivirus NS2B/NS3 protease
noviembre 29, 2022
Author(s):
Jacqueto Zephyr,Desaboini Nageswara Rao,Colby Johnson,Ala M Shaqra,Ellen A Nalivaika,Aria Jordan,Nese Kurt Yilmaz,Akbar Ali,Celia A Schiffer
Source:
Bioorganic chemistry
Viruses from the Flavivirus genus infect millions of people worldwide and cause severe diseases, including recent epidemics of dengue virus (DENV), and Zika virus (ZIKV). There is currently no antivir...
Structure of the catalytically active APOBEC3G bound to a DNA oligonucleotide inhibitor reveals tetrahedral geometry of the transition state
noviembre 19, 2022
Author(s):
Atanu Maiti,Adam K Hedger,Wazo Myint,Vanivilasini Balachandran,Jonathan K Watts,Celia A Schiffer,Hiroshi Matsuo
Source:
Nature communications
APOBEC3 proteins (A3s) are enzymes that catalyze the deamination of cytidine to uridine in single-stranded DNA (ssDNA) substrates, thus playing a key role in innate antiviral immunity. However, the AP...
Dual Inhibitors of Main Protease (MPro) and Cathepsin L as Potent Antivirals against SARS-CoV2
noviembre 10, 2022
Author(s):
Santanu Mondal,Yongzhi Chen,Gordon J Lockbaum,Sudeshna Sen,Sauradip Chaudhuri,Archie C Reyes,Jeong Min Lee,Arshia N Kaur,Nadia Sultana,Michael D Cameron,Scott A Shaffer,Celia A Schiffer,Katherine A Fi...
Source:
Journal of the American Chemical Society
Given the current impact of SARS-CoV2 and COVID-19 on human health and the global economy, the development of direct acting antivirals is of paramount importance. Main protease (M^(Pro)), a cysteine p...
Mucosal nanobody IgA as inhalable and affordable prophylactic and therapeutic treatment against SARS-CoV-2 and emerging variants
septiembre 29, 2022
Author(s):
Qi Li,Fiachra Humphries,Roxie C Girardin,Aaron Wallace,Monir Ejemel,Alla Amcheslavsky,Conor T McMahon,Zachary A Schiller,Zepei Ma,John Cruz,Alan P Dupuis,Anne F Payne,Arooma Maryam,Nese Kurt Yilmaz,Ka...
Source:
Frontiers in immunology
Anti-COVID antibody therapeutics have been developed but not widely used due to their high cost and escape of neutralization from the emerging variants. Here, we describe the development of VHH-IgA1.1...
Defining the substrate envelope of SARS-CoV-2 main protease to predict and avoid drug resistance
junio 21, 2022
Author(s):
Ala M Shaqra,Sarah N Zvornicanin,Qiu Yu J Huang,Gordon J Lockbaum,Mark Knapp,Laura Tandeske,David T Bakan,Julia Flynn,Daniel N A Bolon,Stephanie Moquin,Dustin Dovala,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Nature communications
Coronaviruses can evolve and spread rapidly to cause severe disease morbidity and mortality, as exemplified by SARS-CoV-2 variants of the COVID-19 pandemic. Although currently available vaccines remai...
Comprehensive fitness landscape of SARS-CoV-2 Mpro reveals insights into viral resistance mechanisms
junio 20, 2022
Author(s):
Julia M Flynn,Neha Samant,Gily Schneider-Nachum,David T Barkan,Nese Kurt Yilmaz,Celia A Schiffer,Stephanie A Moquin,Dustin Dovala,Daniel N A Bolon
Source:
eLife
With the continual evolution of new strains of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) that are more virulent, transmissible, and able to evade current vaccines, there is an urgen...
HIV-1 VIF and human APOBEC3G interaction directly observed through molecular specific labeling using a new dual promotor vector
mayo 13, 2022
Author(s):
Wazo Myint,Celia A Schiffer,Hiroshi Matsuo
Source:
Journal of magnetic resonance (San Diego, Calif. : 1997)
Over the last few decades, protein NMR isotope labeling methods using E. coli based expression have revolutionized the information accessible from biomolecular NMR experiments. Selective labeling of a...
Analyses of HIV proteases variants at the threshold of viability reveals relationships between processing efficiency and fitness
marzo 18, 2022
Author(s):
Gily Schneider-Nachum,Julia Flynn,David Mavor,Celia A Schiffer,Daniel N A Bolon
Source:
Virus evolution
Investigating the relationships between protein function and fitness provides keys for understanding biochemical mechanisms that underly evolution. Mutations with partial fitness defects can delineate...
Quantitative structural analysis of influenza virus by cryo-electron tomography and convolutional neural networks
marzo 15, 2022
Author(s):
Qiuyu J Huang,Kangkang Song,Chen Xu,Daniel N A Bolon,Jennifer P Wang,Robert W Finberg,Celia A Schiffer,Mohan Somasundaran
Source:
Structure (London, England : 1993)
Influenza viruses pose severe public health threats globally. Influenza viruses are extensively pleomorphic, in shape, size, and organization of viral proteins. Analysis of influenza morphology and ul...
Call for Papers: Drug Resistance in Infectious Diseases and Beyond
marzo 09, 2022
Author(s):
Celia A Schiffer,Daria J Hazuda
Source:
ACS infectious diseases
No abstract
Deciphering the Molecular Mechanism of HCV Protease Inhibitor Fluorination as a General Approach to Avoid Drug Resistance
febrero 20, 2022
Author(s):
Jacqueto Zephyr,Desaboini Nageswara Rao,Sang V Vo,Mina Henes,Klajdi Kosovrasti,Ashley N Matthew,Adam K Hedger,Jennifer Timm,Elise T Chan,Akbar Ali,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Journal of molecular biology
Third generation Hepatitis C virus (HCV) NS3/4A protease inhibitors (PIs), glecaprevir and voxilaprevir, are highly effective across genotypes and against many resistant variants. Unlike earlier PIs, ...
Identification of a Permissive Secondary Mutation That Restores the Enzymatic Activity of Oseltamivir Resistance Mutation H275Y
enero 19, 2022
Author(s):
Li Jiang,Neha Samant,Ping Liu,Mohan Somasundaran,Jeffrey D Jensen,Wayne A Marasco,Timothy F Kowalik,Celia A Schiffer,Robert W Finberg,Jennifer P Wang,Daniel N A Bolon
Source:
Journal of virology
Many oseltamivir resistance mutations exhibit fitness defects in the absence of drug pressure that hinders their propagation in hosts. Secondary permissive mutations can rescue fitness defects and fac...
Viral proteases: Structure, mechanism and inhibition
diciembre 04, 2021
Author(s):
Jacqueto Zephyr,Nese Kurt Yilmaz,Celia A Schiffer
Source:
The Enzymes
Viral proteases are diverse in structure, oligomeric state, catalytic mechanism, and substrate specificity. This chapter focuses on proteases from viruses that are relevant to human health: human immu...
Pan-3C Protease Inhibitor Rupintrivir Binds SARS-CoV-2 Main Protease in a Unique Binding Mode
septiembre 10, 2021
Author(s):
Gordon J Lockbaum,Mina Henes,Jeong Min Lee,Jennifer Timm,Ellen A Nalivaika,Paul R Thompson,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Biochemistry
Rupintrivir targets the 3C cysteine proteases of the picornaviridae family, which includes rhinoviruses and enteroviruses that cause a range of human diseases. Despite being a pan-3C protease inhibito...
Discovery of Quinoxaline-Based P1-P3 Macrocyclic NS3/4A Protease Inhibitors with Potent Activity against Drug-Resistant Hepatitis C Virus Variants
agosto 18, 2021
Author(s):
Desaboini Nageswara Rao,Jacqueto Zephyr,Mina Henes,Elise T Chan,Ashley N Matthew,Adam K Hedger,Hasahn L Conway,Mohsan Saeed,Alicia Newton,Christos J Petropoulos,Wei Huang,Nese Kurt Yilmaz,Celia A Schi...
Source:
Journal of medicinal chemistry
The three pan-genotypic HCV NS3/4A protease inhibitors (PIs) currently in clinical use-grazoprevir, glecaprevir, and voxilaprevir-are quinoxaline-based P2-P4 macrocycles and thus exhibit similar resis...
Affinity maturation of SARS-CoV-2 neutralizing antibodies confers potency, breadth, and resilience to viral escape mutations
julio 31, 2021
Author(s):
Frauke Muecksch,Yiska Weisblum,Christopher O Barnes,Fabian Schmidt,Dennis Schaefer-Babajew,Zijun Wang,Julio C C Lorenzi,Andrew I Flyak,Andrew T DeLaitsch,Kathryn E Huey-Tubman,Shurong Hou,Celia A Schi...
Source:
Immunity
Antibodies elicited by infection accumulate somatic mutations in germinal centers that can increase affinity for cognate antigens. We analyzed 6 independent groups of clonally related severe acute res...
Structural basis of substrate specificity in human cytidine deaminase family APOBEC3s
junio 25, 2021
Author(s):
Shurong Hou,Jeong Min Lee,Wazo Myint,Hiroshi Matsuo,Nese Kurt Yilmaz,Celia A Schiffer
Source:
The Journal of biological chemistry
The human cytidine deaminase family of APOBEC3s (A3s) plays critical roles in both innate immunity and the development of cancers. A3s comprise seven functionally overlapping but distinct members that...
Deciphering Antifungal Drug Resistance in Pneumocystis jirovecii DHFR with Molecular Dynamics and Machine Learning
junio 17, 2021
Author(s):
Florian Leidner,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Journal of chemical information and modeling
Drug resistance impacts the effectiveness of many new therapeutics. Mutations in the therapeutic target confer resistance; however, deciphering which mutations, often remote from the enzyme active sit...
Report of the National Institutes of Health SARS-CoV-2 Antiviral Therapeutics Summit
junio 10, 2021
Author(s):
Matthew D Hall,James M Anderson,Annaliesa Anderson,David Baker,Jay Bradner,Kyle R Brimacombe,Elizabeth A Campbell,Kizzmekia S Corbett,Kara Carter,Sara Cherry,Lillian Chiang,Tomas Cihlar,Emmie de Wit,M...
Source:
The Journal of infectious diseases
The NIH Virtual SARS-CoV-2 Antiviral Summit, held on 6 November 2020, was organized to provide an overview on the status and challenges in developing antiviral therapeutics for coronavirus disease 201...
Deciphering Complex Mechanisms of Resistance and Loss of Potency through Coupled Molecular Dynamics and Machine Learning
marzo 30, 2021
Author(s):
Florian Leidner,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Journal of chemical theory and computation
Drug resistance threatens many critical therapeutics through mutations in the drug target. The molecular mechanisms by which combinations of mutations, especially those remote from the active site, al...
Development of potency, breadth and resilience to viral escape mutations in SARS-CoV-2 neutralizing antibodies
marzo 24, 2021
Author(s):
Frauke Muecksch,Yiska Weisblum,Christopher O Barnes,Fabian Schmidt,Dennis Schaefer-Babajew,Julio C C Lorenzi,Andrew I Flyak,Andrew T DeLaitsch,Kathryn E Huey-Tubman,Shurong Hou,Celia A Schiffer,Christ...
Source:
bioRxiv : the preprint server for biology
Antibodies elicited in response to infection undergo somatic mutation in germinal centers that can result in higher affinity for the cognate antigen. To determine the effects of somatic mutation on th...
Introduction: Drug Resistance
marzo 24, 2021
Author(s):
Nese Kurt Yilmaz,Celia A Schiffer
Source:
Chemical reviews
No abstract
Inhibiting HTLV-1 Protease: A Viable Antiviral Target
febrero 23, 2021
Author(s):
Gordon J Lockbaum,Mina Henes,Nathaniel Talledge,Linah N Rusere,Klajdi Kosovrasti,Ellen A Nalivaika,Mohan Somasundaran,Akbar Ali,Louis M Mansky,Nese Kurt Yilmaz,Celia A Schiffer
Source:
ACS chemical biology
Human T-cell lymphotropic virus type 1 (HTLV-1) is a retrovirus that can cause severe paralytic neurologic disease and immune disorders as well as cancer. An estimated 20 million people worldwide are ...
NAD(H) phosphates mediate tetramer assembly of human C-terminal binding protein (CtBP)
febrero 01, 2021
Author(s):
Jeffry C Nichols,Celia A Schiffer,William E Royer
Source:
The Journal of biological chemistry
C-terminal binding proteins (CtBPs) are cotranscriptional factors that play key roles in cell fate. We have previously shown that NAD(H) promotes the assembly of similar tetramers from either human Ct...
Crystal Structure of SARS-CoV-2 Main Protease in Complex with the Non-Covalent Inhibitor ML188
enero 28, 2021
Author(s):
Gordon J Lockbaum,Archie C Reyes,Jeong Min Lee,Ronak Tilvawala,Ellen A Nalivaika,Akbar Ali,Nese Kurt Yilmaz,Paul R Thompson,Celia A Schiffer
Source:
Viruses
Viral proteases are critical enzymes for the maturation of many human pathogenic viruses and thus are key targets for direct acting antivirals (DAAs). The current viral pandemic caused by SARS-CoV-2 i...
Unique structural solution from a VH3-30 antibody targeting the hemagglutinin stem of influenza A viruses
enero 26, 2021
Author(s):
Wayne D Harshbarger,Derrick Deming,Gordon J Lockbaum,Nattapol Attatippaholkun,Maliwan Kamkaew,Shurong Hou,Mohan Somasundaran,Jennifer P Wang,Robert W Finberg,Quan Karen Zhu,Celia A Schiffer,Wayne A Ma...
Source:
Nature communications
Broadly neutralizing antibodies (bnAbs) targeting conserved influenza A virus (IAV) hemagglutinin (HA) epitopes can provide valuable information for accelerating universal vaccine designs. Here, we re...
Interactions of APOBEC3s with DNA and RNA
enero 24, 2021
Author(s):
Atanu Maiti,Shurong Hou,Celia A Schiffer,Hiroshi Matsuo
Source:
Current opinion in structural biology
APOBEC3 enzymes are key enzymes in our innate immune system regulating antiviral response in HIV and unfortunately adding diversity in cancer as they deaminate cytosine. Seven unique single and double...
Drug Design Strategies to Avoid Resistance in Direct-Acting Antivirals and Beyond
enero 07, 2021
Author(s):
Ashley N Matthew,Florian Leidner,Gordon J Lockbaum,Mina Henes,Jacqueto Zephyr,Shurong Hou,Desaboini Nageswara Rao,Jennifer Timm,Linah N Rusere,Debra A Ragland,Janet L Paulsen,Kristina Prachanronarong,...
Source:
Chemical reviews
Drug resistance is prevalent across many diseases, rendering therapies ineffective with severe financial and health consequences. Rather than accepting resistance after the fact, proactive strategies ...
Cryo-EM structure of CtBP2 confirms tetrameric architecture
diciembre 02, 2020
Author(s):
Anne M Jecrois,M Michael Dcona,Xiaoyan Deng,Dipankar Bandyopadhyay,Steven R Grossman,Celia A Schiffer,William E Royer
Source:
Structure (London, England : 1993)
C-terminal binding proteins 1 and 2 (CtBP1 and CtBP2) are transcriptional regulators that activate or repress many genes involved in cellular development, apoptosis, and metastasis. NADH-dependent CtB...
Crystal Structure of a Soluble APOBEC3G Variant Suggests ssDNA to Bind in a Channel that Extends between the Two Domains
octubre 25, 2020
Author(s):
Atanu Maiti,Wazo Myint,Krista A Delviks-Frankenberry,Shurong Hou,Tapan Kanai,Vanivilasini Balachandran,Christina Sierra Rodriguez,Rashmi Tripathi,Nese Kurt Yilmaz,Vinay K Pathak,Celia A Schiffer,Hiros...
Source:
Journal of molecular biology
APOBEC3G (A3G) is a single-stranded DNA (ssDNA) cytosine deaminase that can restrict HIV-1 infection by mutating the viral genome. A3G consists of a non-catalytic N-terminal domain (NTD) and a catalyt...
A cross-reactive human IgA monoclonal antibody blocks SARS-CoV-2 spike-ACE2 interaction
agosto 23, 2020
Author(s):
Monir Ejemel,Qi Li,Shurong Hou,Zachary A Schiller,Julia A Tree,Aaron Wallace,Alla Amcheslavsky,Nese Kurt Yilmaz,Karen R Buttigieg,Michael J Elmore,Kerry Godwin,Naomi Coombes,Jacqueline R Toomey,Ryan S...
Source:
Nature communications
COVID-19 caused by SARS-CoV-2 has become a global pandemic requiring the development of interventions for the prevention or treatment to curtail mortality and morbidity. No vaccine to boost mucosal im...
Genome-scale in vivo CRISPR screen identifies RNLS as a target for beta cell protection in type 1 diabetes
julio 29, 2020
Author(s):
Erica P Cai,Yuki Ishikawa,Wei Zhang,Nayara C Leite,Jian Li,Shurong Hou,Badr Kiaf,Jennifer Hollister-Lock,Nese Kurt Yilmaz,Celia A Schiffer,Douglas A Melton,Stephan Kissler,Peng Yi
Source:
Nature metabolism
Type 1 diabetes (T1D) is caused by the autoimmune destruction of pancreatic beta cells. Pluripotent stem cells can now be differentiated into beta cells, thus raising the prospect of a cell replacemen...
Structural Analysis of Potent Hybrid HIV-1 Protease Inhibitors Containing Bis-tetrahydrofuran in a Pseudosymmetric Dipeptide Isostere
julio 17, 2020
Author(s):
Linah N Rusere,Gordon J Lockbaum,Mina Henes,Sook-Kyung Lee,Ean Spielvogel,Desaboini Nageswara Rao,Klajdi Kosovrasti,Ellen A Nalivaika,Ronald Swanstrom,Nese Kurt Yilmaz,Celia A Schiffer,Akbar Ali
Source:
Journal of medicinal chemistry
The design, synthesis, and X-ray structural analysis of hybrid HIV-1 protease inhibitors (PIs) containing bis-tetrahydrofuran (bis-THF) in a pseudo-C(2)-symmetric dipeptide isostere are described. A s...
IgA MAb blocks SARS-CoV-2 Spike-ACE2 interaction providing mucosal immunity
junio 09, 2020
Author(s):
Monir Ejemel,Qi Li,Shurong Hou,Zachary A Schiller,Aaron L Wallace,Alla Amcheslavsky,Nese Kurt Yilmaz,Jacqueline R Toomey,Ryan Schneider,Brianna J Close,Da-Yuan Chen,Hasahn L Conway,Saeed Mohsan,Lisa A...
Source:
bioRxiv : the preprint server for biology
COVID-19 caused by SARS-CoV-2 has become a global pandemic requiring the development of interventions for the prevention or treatment to curtail mortality and morbidity. No vaccine to boost mucosal im...
Avoiding Drug Resistance by Substrate Envelope-Guided Design: Toward Potent and Robust HCV NS3/4A Protease Inhibitors
abril 03, 2020
Author(s):
Ashley N Matthew,Jacqueto Zephyr,Desaboini Nageswara Rao,Mina Henes,Wasih Kamran,Klajdi Kosovrasti,Adam K Hedger,Gordon J Lockbaum,Jennifer Timm,Akbar Ali,Nese Kurt Yilmaz,Celia A Schiffer
Source:
mBio
Hepatitis C virus (HCV) infects millions of people worldwide, causing chronic liver disease that can lead to cirrhosis, hepatocellular carcinoma, and liver transplant. In the last several years, the a...
Optimizing the refinement of merohedrally twinned P61 HIV-1 protease-inhibitor cocrystal structures
marzo 06, 2020
Author(s):
Gordon J Lockbaum,Florian Leidner,William E Royer,Nese Kurt Yilmaz,Celia A Schiffer
Source:
Acta crystallographica. Section D, Structural biology
Twinning is a crystal-growth anomaly in which protein monomers exist in different orientations but are related in a specific way, causing diffraction reflections to overlap. Twinning imposes additiona...
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Overview: Drug Resistance
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Introducing Sequence Diversity: APOBEC3s
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