Amy Diallo

ORCID: 0000-0001-9843-2255
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About
Contact & Profiles
Research Areas
  • SARS-CoV-2 and COVID-19 Research
  • Monoclonal and Polyclonal Antibodies Research
  • vaccines and immunoinformatics approaches
  • interferon and immune responses
  • Protein Degradation and Inhibitors
  • Computational Drug Discovery Methods
  • Chromatin Remodeling and Cancer
  • RNA and protein synthesis mechanisms
  • Nematode management and characterization studies
  • Global Health and Surgery
  • COVID-19 Clinical Research Studies
  • Bioinformatics and Genomic Networks
  • Competency Development and Evaluation
  • SARS-CoV-2 detection and testing
  • Counseling Practices and Supervision
  • Immunodeficiency and Autoimmune Disorders
  • Biomedical and Engineering Education
  • Poxvirus research and outbreaks
  • Mitochondrial Function and Pathology
  • Genetics, Bioinformatics, and Biomedical Research
  • Protist diversity and phylogeny
  • Bacteriophages and microbial interactions
  • Click Chemistry and Applications
  • Machine Learning in Bioinformatics
  • Synthesis and biological activity

University of California, San Francisco
2020-2025

Quantitative BioSciences
2021-2022

Molecular Biology Consortium
2020-2021

University of San Francisco
2021

David E. Gordon Joseph Hiatt Mehdi Bouhaddou Veronica V. Rezelj Svenja Ulferts and 95 more Hannes Braberg Alexander S. Jureka Kirsten Obernier Jeffrey Guo Jyoti Batra Robyn M. Kaake Andrew R. Weckstein Tristan W. Owens Meghna Gupta Sergei Pourmal Erron W. Titus Merve Çakır Margaret Soucheray Michael McGregor Zeynep Cakir Gwendolyn Μ. Jang Matthew J. O’Meara Tia A. Tummino Ziyang Zhang Helene Foussard Ajda Rojc Yuan Zhou Dmitry Kuchenov Ruth Hüttenhain Jiewei Xu Manon Eckhardt Danielle L. Swaney Jacqueline M. Fabius Manisha R. Ummadi Beril Tutuncuoglu Ujjwal Rathore Maya Modak Paige Haas Kelsey M. Haas Zun Zar Chi Naing Ernst H. Pulido Ying Shi Inigo Barrio‐Hernandez Danish Memon Eirini Petsalaki Alistair S. Dunham Miguel Marrero David F. Burke Cassandra Koh Thomas Vallet Jesus A. Silvas Caleigh M. Azumaya Christian B. Billesbølle Axel F. Brilot Melody G. Campbell Amy Diallo Miles Sasha Dickinson Devan Diwanji Nadia Herrera Nick Hoppe Huong T. Kratochvil Yanxin Liu Gregory E. Merz Michelle Moritz Henry C. Nguyen Carlos Nowotny Cristina Puchades Alexandrea N. Rizo Ursula Schulze‐Gahmen Amber M. Smith Ming Sun I.D. Young Jianhua Zhao Daniel Asarnow J.T. Biel Alisa Bowen Julian R. Braxton Jen Chen Cynthia M. Chio Un Seng Chio Ishan Deshpande Loan Doan Bryan Faust Sebastián Flores Mingliang Jin Kate Kim Victor L. Lam Fei Li Junrui Li Yen-Li Li Yang Li Xi Liu Megan Lo Kyle E. Lopez Arthur A. Melo Frank R. Moss Phuong Nguyen Joana Paulino Komal Ishwar Pawar Jessica K. Peters

The COVID-19 pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is a grave threat to public health and the global economy. SARS-CoV-2 closely related more lethal but less transmissible coronaviruses SARS-CoV-1 Middle East (MERS-CoV). Here, we have carried out comparative viral-human protein-protein interaction viral protein localization analyses for all three viruses. Subsequent functional genetic screening identified host factors that functionally impinge on...

10.1126/science.abe9403 article EN cc-by Science 2020-10-15

10.1038/s41589-020-00679-1 article EN other-oa Nature Chemical Biology 2020-10-20

Abstract The SARS-CoV-2 protein Nsp2 has been implicated in a wide range of viral processes, but its exact functions, and the structural basis those remain unknown. Here, we report an atomic model for full-length obtained by combining cryo-electron microscopy with deep learning-based structure prediction from AlphaFold2. resulting reveals highly-conserved zinc ion-binding site, suggesting role RNA binding. Mapping emerging mutations variants on shows potential host-Nsp2 interaction regions....

10.1101/2021.05.10.443524 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-05-12

The main protease (MPro) of SARS-CoV-2 is crucial for viral replication and the target nirmatrelvir (the active ingredient Paxlovid) ensitrelvir. identification new agents with differentiated pharmacokinetic drug resistance profiles will increase therapeutic options COVID-19 patients bolster pandemic preparedness generally. Starting a lead-like dihydrouracil chemotype from large-library docking campaign, we improved MPro inhibition >1,000 fold by engaging additional subsites in site, most...

10.1101/2025.01.16.633443 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2025-01-18

Inhibitors of bromodomain and extraterminal domain (BET) proteins are possible anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) prophylactics as they downregulate angiotensin-converting enzyme (ACE2). Here we show that BET should not be inactivated therapeutically because critical antiviral factors at the post-entry level. Depletion BRD3 or BRD4 in cells overexpressing ACE2 exacerbates SARS-CoV-2 infection; same is observed when with endogenous expression treated inhibitors...

10.1016/j.celrep.2022.111088 article EN cc-by-nc-nd Cell Reports 2022-06-27

The SARS-CoV-2 protein Nsp2 has been implicated in a wide range of viral processes, but its exact functions, and the structural basis those remain unknown. Here, we report an atomic model for full-length obtained by combining cryo-electron microscopy with deep learning-based structure prediction from AlphaFold2. resulting reveals highly-conserved zinc ion-binding site, suggesting role RNA binding. Mapping emerging mutations variants on shows potential host-Nsp2 interaction regions. Using...

10.21203/rs.3.rs-515215/v1 preprint EN cc-by Research Square (Research Square) 2021-05-19

Inhibitors of Bromodomain and Extra-terminal domain (BET) proteins are possible anti-SARS-CoV-2 prophylactics as they downregulate angiotensin-converting enzyme 2 (ACE2). Here, we show that BET should not be inactivated therapeutically critical antiviral factors at the post-entry level. Knockouts BRD3 or BRD4 in cells overexpressing ACE2 exacerbate SARS-CoV-2 infection; same is observed when with endogenous expression treated inhibitors during infection, before. Viral replication mortality...

10.1101/2021.11.14.468537 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-11-15

Science education and research have the potential to drive profound change in low- middle-income countries (LMICs) through encouraging innovation, attracting industry, creating job opportunities. However, LMICs, capacity is often limited, acquisition of funding access state-of-the-art technologies challenging. The Alliance for Global Health (the Alliance) was founded as a partnership between University California, Berkeley (USA) Makerere (Uganda), with goal strengthening University's...

10.1080/16549716.2022.2062175 article EN cc-by Global Health Action 2022-06-22
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