A convenient cell fusion assay for the study of SARS‐CoV entry and inhibition
Autor: | Ying Zhu, Da He Jiang, Wen Lan Wu, Xin Mao, Rui Gong, Zhi Jian Cao, Wenxin Li, Ying Liang Wu, Hui Liu, Xiu Ling Xu, Yong Gang Sha |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2008 |
Předmět: |
fusion inhibition
Time Factors viruses Clinical Biochemistry Green Fluorescent Proteins ACE2 Biology Peptidyl-Dipeptidase A Severe Acute Respiratory Syndrome Biochemistry Article Flow cytometry S protein Cell Fusion Viral Envelope Proteins Viral entry Chlorocebus aethiops Genetics medicine Escherichia coli Animals Trypsin cell‐to‐cell fusion assay Molecular Biology Fluorescent Dyes Glutathione Transferase Syncytium COS cells Cell fusion Membrane Glycoproteins medicine.diagnostic_test Ligand binding assay SARS‐CoV Cell Biology Articles Molecular biology Coculture Techniques Recombinant Proteins Cell biology Luminescent Proteins Severe acute respiratory syndrome-related coronavirus Cell culture COS Cells Spike Glycoprotein Coronavirus Biological Assay Angiotensin-Converting Enzyme 2 Peptides Fusion mechanism |
Zdroj: | Iubmb Life |
ISSN: | 1521-6551 1521-6543 |
Popis: | SARS‐CoV spike (S) protein‐mediated cell fusion is important for the viral entry mechanism and identification of SARS‐CoV entry inhibitors. In order to avoid the high risks involved in handling SARS‐CoV and to facilitate the study of viral fusion mechanism, we established the cell lines: SR‐COS7 cells that stably express both SARS‐CoV S protein and red fluorescence protein, R‐COS7 cells that stably express red fluorescence protein, and AG‐COS7 cells that stably express both ACE2 and green fluorescence protein, respectively. When SR‐COS7 cells or R‐COS7 cells were cocultured with AG‐COS7 cells, syncytia with yellow fluorescence were conveniently observed after 12 h in SR‐COS7 cells plus AG‐COS7 cells, but not in R‐COS7 cells plus AG‐COS7 cells. The cell‐to‐cell fusion efficiency was simply determined for quantitative analysis based on the number of syncytium detected by flow cytometry. Such new cell‐to‐cell fusion model was further assessed by the potent HR2 peptide inhibitor, which led to the obvious decrease of the cell‐to‐cell fusion efficiency. The successful fusion and inhibition of cell‐based binding assay shows that it can be well used for the study of SARS‐CoV entry and inhibition. iubmb Life, 58: 480 ‐ 486, 2006 |
Databáze: | OpenAIRE |
Externí odkaz: |