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Biochem Biophys Res Commun. 2000 Dec 20;279(2):557-62.

The RNA aptamer-binding site of hepatitis C virus NS3 protease.

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  • 1National Institute of Bioscience & Human Technology, Tsukuba, Ibaraki, 305-8566, Japan.

Abstract

Nonstructural protein 3 (NS3) of hepatitis C virus (HCV) is a trypsin-like protease and is essential for processing of viral polyprotein. Accordingly, it is a potential target for anti-HCV drugs. Recently we could isolate RNA aptamers (G9-I, II, and III) which bind and inhibit NS3 protease using in vitro selection strategy. In addition, G9-I aptamer showed noncompetitive inhibition. In order to elucidate the binding site of G9-I aptamer in NS3 protease domain (deltaNS3), we carried out alanine scanning mutagenesis at positive charged residues on the surface of deltaNS3. The result of binding analysis by surface plasmon resonance measurements and protease inhibition assay clarified that Arg161 as well as Arg130 of deltaNS3 are essential for interaction with G9-I aptamer. This region appears to be a potential targeting site for anti-HCV drugs.

Copyright 2000 Academic Press.

PMID:
11118325
[PubMed - indexed for MEDLINE]
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