A high-throughput approach to evaluating NCp7 RNA binding activity for HIV-1 drug discovery

The HIV-1 epidemic broadly impacts healthcare. There remains a continued need for improved anti-viral therapies resilient to the development of drug resistance. HIV-1 nucleocapsid protein 7 (NCp7) seems a prime drug target due to its unique nucleic acid chaperone activity required for multiple viral processes. NCp7 RNA binding activity has been shown to increase viral production and infectivity within the host. Here we introduce a high-throughput AlphaScreen assay to evaluate NCp7 RNA binding activity and validate its specificity and sensitivity using a known inhibitor. We also demonstrate the utility of this assay by performing a drug-repurposing screen, which identified seven confirmed inhibitors of NCp7 RNA binding and two confirmed enhancers of NCp7 RNA binding. This tool will aid in future NCp7-targeted drug discovery initiatives for the treatment of HIV-1 infection.

Authors

Institutions

Publication Details

Journal
SLAS DISCOVERY
Published
2025-08-11
DOI
https://doi.org/10.1016/j.slasd.2025.100260
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A high-throughput approach to evaluating NCp7 RNA binding activity for HIV-1 drug discovery

Joanna K. Winstone, Rikki L. Uhrich, Thibault Alle, Brian C. Kraemer
SLAS DISCOVERY
HIV Research and Treatment
article

A high-throughput approach to evaluating NCp7 RNA binding activity for HIV-1 drug discovery

Joanna K. Winstone, Rikki L. Uhrich, Thibault Alle, Brian C. Kraemer
article en

Abstract

The HIV-1 epidemic broadly impacts healthcare. There remains a continued need for improved anti-viral therapies resilient to the development of drug resistance. HIV-1 nucleocapsid protein 7 (NCp7) seems a prime drug target due to its unique nucleic acid chaperone activity required for multiple viral processes. NCp7 RNA binding activity has been shown to increase viral production and infectivity within the host. Here we introduce a high-throughput AlphaScreen assay to evaluate NCp7 RNA binding activity and validate its specificity and sensitivity using a known inhibitor. We also demonstrate the utility of this assay by performing a drug-repurposing screen, which identified seven confirmed inhibitors of NCp7 RNA binding and two confirmed enhancers of NCp7 RNA binding. This tool will aid in future NCp7-targeted drug discovery initiatives for the treatment of HIV-1 infection.

SLAS DISCOVERYVol. 35
University of Puget Sound (US), University of Washington (US), Skagit Valley Hospital (US), VA Puget Sound Health Care System (US), Geriatric Research Education and Clinical Center (US), University of Montana (US)
Foundation for the National Institutes of Health, U.S. Department of Veterans Affairs, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 77%
HIV Research and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.