Area of research
Infectious Diseases · Virology · Machi
Research interest
Research interests include HIV/AIDS drug development and treatment, HIV Research and Treatment, HIV/AIDS Research and Interventions, and Hepatitis C virus research.
A novel corneal epithelial cell culture assay for assessing topical antivirals against herpes simplex virus keratitis.
HIV-1 usurps mixed-charge domain-dependent CPSF6 phase separation for higher-order capsid binding, nuclear entry and viral DNA integration
The HIV-1 capsid core is an opportunistic nuclear import receptor
Multidisciplinary studies with mutated HIV-1 capsid proteins reveal structural mechanisms of lattice stabilization
Discovery of Nirmatrelvir Resistance Mutations in SARS-CoV-2 3CLpro: A Computational-Experimental Approach
Biochemical and structural insights into SARS-CoV-2 polyprotein processing by Mpro
Marine Natural Products as Leads against SARS-CoV-2 Infection
Baicalein and Baicalin Inhibit SARS-CoV-2 RNA-Dependent-RNA Polymerase
Avoiding Drug Resistance in HIV Reverse Transcriptase
The SMC5/6 complex compacts and silences unintegrated HIV-1 DNA and is antagonized by Vpr
Rotten to the core: antivirals targeting the HIV-1 capsid core
Comparison of anti-SARS-CoV-2 activity and intracellular metabolism of remdesivir and its parent nucleoside
HIV-1 replication complexes accumulate in nuclear speckles and integrate into speckle-associated genomic domains
Feasibility of Known RNA Polymerase Inhibitors as Anti-SARS-CoV-2 Drugs
Novel PF74-like small molecules targeting the HIV-1 capsid protein: Balance of potency and metabolic stability
Toward Structurally Novel and Metabolically Stable HIV-1 Capsid-Targeting Small Molecules
Novel HIV-1 capsid-targeting small molecules of the PF74 binding site
Chemical profiling of HIV-1 capsid-targeting antiviral PF74
Glycosylated diphyllin as a broad-spectrum antiviral agent against Zika virus
Cutting into the Substrate Dominance: Pharmacophore and Structure-Based Approaches toward Inhibiting Human Immunodeficiency Virus Reverse Transcriptase-Associated Ribonuclease H
Long-Acting Anti-HIV Drugs Targeting HIV-1 Reverse Transcriptase and Integrase
4′-Ethynyl-2-fluoro-2′-deoxyadenosine, MK-8591
Small Molecule Inhibitor that Stabilizes the Autoinhibited Conformation of the Oncogenic Tyrosine Phosphatase SHP2
6-Arylthio-3-hydroxypyrimidine-2,4-diones potently inhibited HIV reverse transcriptase-associated RNase H with antiviral activity
6-Biphenylmethyl-3-hydroxypyrimidine-2,4-diones potently and selectively inhibited HIV reverse transcriptase-associated RNase H
The High Genetic Barrier of EFdA/MK-8591 Stems from Strong Interactions with the Active Site of Drug-Resistant HIV-1 Reverse Transcriptase
Structural Implications of Genotypic Variations in HIV-1 Integrase From Diverse Subtypes
Multiplex single-cell visualization of nucleic acids and protein during HIV infection
Oral Administration of the Nucleoside EFdA (4′-Ethynyl-2-Fluoro-2′-Deoxyadenosine) Provides Rapid Suppression of HIV Viremia in Humanized Mice and Favorable Pharmacokinetic Properties in Mice and the Rhesus Macaque
SAMHD1 Has Differential Impact on the Efficacies of HIV Nucleoside Reverse Transcriptase Inhibitors