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. 1996 Oct;70(10):6694-700.
doi: 10.1128/JVI.70.10.6694-6700.1996.

Activity of purified hepatitis C virus protease NS3 on peptide substrates

C Steinkühler  1 , A Urbani, L Tomei, G Biasiol, M Sardana, E Bianchi, A Pessi, R De Francesco
Affiliations

Activity of purified hepatitis C virus protease NS3 on peptide substrates

C Steinkühler et al. J Virol. 1996 Oct.

Abstract

The protease domain of the hepatitis C virus (HCV) protein NS3 was expressed in Escherichia coli, purified to homogeneity, and shown to be active on peptides derived from the sequence of the NS4A-NS4B junction. Experiments were carried out to optimize protease activity. Buffer requirements included the presence of detergent, glycerol, and dithiothreitol, pH between 7.5 and 8.5, and low ionic strength. C- and N-terminal deletion experiments defined a peptide spanning from the P6 to the P4' residue as a suitable substrate. Cleavage kinetics were subsequently measured by using decamer P6-P4' peptides corresponding to all intermolecular cleavage sites of the HCV polyprotein. The following order of cleavage efficiency, in terms of kcat/Km, was determined: NS5A-NS5B > NS4A-NS4B >> NS4B-NS5A. A 14-mer peptide containing residues 21 to 34 of the protease cofactor NS4A (Pep4A 21-34), when added in stoichiometric amounts, was shown to increase cleavage rates of all peptides, the largest effect (100-fold) being observed on the hydrolysis of the NS4B-NS5A decamer. From the kinetic analysis of cleavage data, we conclude that (i) primary structure is an important determinant of the efficiency with which each site is cleaved during polyprotein processing, (ii) slow cleavage of the NS4B-NS5A site in the absence of NS4A is due to low binding affinity of the enzyme for this site, and (iii) formation of a 1:1 complex between the protease and Pep4A 21-34 is sufficient and required for maximum activation.

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References

    1. Biochem Biophys Res Commun. 1993 Apr 30;192(2):399-406 - PubMed
    1. J Gen Virol. 1995 Jul;76 ( Pt 7):1729-36 - PubMed
    1. J Virol. 1993 Jul;67(7):4017-26 - PubMed
    1. J Virol. 1993 Aug;67(8):4665-75 - PubMed
    1. J Biol Chem. 1993 Dec 5;268(34):25449-54 - PubMed

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