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SARS-CoV-2 Nucleocapsid Protein TR-FRET Assay Amenable to High Throughput Screening.
Gorshkov, Kirill; Morales Vasquez, Desarey; Chiem, Kevin; Ye, Chengjin; Nguyen Tran, Bruce; Carlos de la Torre, Juan; Moran, Thomas; Chen, Catherine Z; Martinez-Sobrido, Luis; Zheng, Wei.
Affiliation
  • Gorshkov K; National Center for Advancing Translational Sciences, 9800 Medical Center Drive, Rockville, Maryland 20850, United States.
  • Morales Vasquez D; Texas Biomedical Research Institute, 8715 West Military Drive, San Antonio, Texas 78227, United States.
  • Chiem K; Texas Biomedical Research Institute, 8715 West Military Drive, San Antonio, Texas 78227, United States.
  • Ye C; Texas Biomedical Research Institute, 8715 West Military Drive, San Antonio, Texas 78227, United States.
  • Nguyen Tran B; National Center for Advancing Translational Sciences, 9800 Medical Center Drive, Rockville, Maryland 20850, United States.
  • Carlos de la Torre J; Department of Immunology and Microbiology, IMM6, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
  • Moran T; Icahn School of Medicine, Mt. Sinai, 1 Gustave L. Levy Place, New York, New York 10029, United States.
  • Chen CZ; National Center for Advancing Translational Sciences, 9800 Medical Center Drive, Rockville, Maryland 20850, United States.
  • Martinez-Sobrido L; Texas Biomedical Research Institute, 8715 West Military Drive, San Antonio, Texas 78227, United States.
  • Zheng W; National Center for Advancing Translational Sciences, 9800 Medical Center Drive, Rockville, Maryland 20850, United States.
ACS Pharmacol Transl Sci ; 5(1): 8-19, 2022 Jan 14.
Article in En | MEDLINE | ID: mdl-35036857
Drug development for specific antiviral agents against coronavirus disease 2019 (COVID-19) is still an unmet medical need as the pandemic continues to spread globally. Although huge efforts for drug repurposing and compound screens have been put forth, only a few compounds are in late-stage clinical trials. New approaches and assays are needed to accelerate COVID-19 drug discovery and development. Here, we report a time-resolved fluorescence resonance energy transfer-based assay that detects the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid protein (NP) produced in infected cells. It uses two specific anti-NP monoclonal antibodies conjugated to donor and acceptor fluorophores that produce a robust ratiometric signal for high throughput screening of large compound collections. Using this assay, we measured a half maximal inhibitory concentration (IC50) for remdesivir of 9.3 µM against infection with SARS-CoV-2 USA/WA1/2020 (WA-1). The assay also detected SARS-CoV-2 South African (Beta, ß), Brazilian/Japanese P.1 (Gamma, γ), and Californian (Epsilon, ε) variants of concern (VoC). Therefore, this homogeneous SARS-CoV-2 NP detection assay can be used for accelerating lead compound discovery for drug development and for evaluating drug efficacy against emerging SARS-CoV-2 VoC.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: ACS Pharmacol Transl Sci Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Screening_studies Language: En Journal: ACS Pharmacol Transl Sci Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos