Unknown

Dataset Information

0

Selectivity in ISG15 and ubiquitin recognition by the SARS coronavirus papain-like protease.


ABSTRACT: The severe acute respiratory syndrome coronavirus papain-like protease (SARS-CoV PLpro) carries out N-terminal processing of the viral replicase polyprotein, and also exhibits Lys48-linked polyubiquitin chain debranching and ISG15 precursor processing activities in vitro. Here, we used SDS-PAGE and fluorescence-based assays to demonstrate that ISG15 derivatives are the preferred substrates for the deubiquitinating activity of the PLpro. With k(cat)/K(M) of 602,000 M(-1)s(-1), PLpro hydrolyzes ISG15-AMC 30- and 60-fold more efficiently than Ub-AMC and Nedd8-AMC, respectively. Data obtained with truncated ISG15 and hybrid Ub/ISG15 substrates indicate that both the N- and C-terminal Ub-like domains of ISG15 contribute to this preference. The enzyme also displays a preference for debranching Lys48- over Lys63-linked polyubiquitin chains. Our results demonstrate that SARS-CoV PLpro can differentiate between ubiquitin-like modifiers sharing a common C-terminal sequence, and that the debranching activity of the PLpro is linkage type selective. The potential structural basis for the demonstrated specificity of SARS-CoV PLpro is discussed.

SUBMITTER: Lindner HA 

PROVIDER: S-EPMC7094341 | biostudies-literature | 2007 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Selectivity in ISG15 and ubiquitin recognition by the SARS coronavirus papain-like protease.

Lindner Holger A HA   Lytvyn Viktoria V   Qi Hongtao H   Lachance Paule P   Ziomek Edmund E   Ménard Robert R  

Archives of biochemistry and biophysics 20070714 1


The severe acute respiratory syndrome coronavirus papain-like protease (SARS-CoV PLpro) carries out N-terminal processing of the viral replicase polyprotein, and also exhibits Lys48-linked polyubiquitin chain debranching and ISG15 precursor processing activities in vitro. Here, we used SDS-PAGE and fluorescence-based assays to demonstrate that ISG15 derivatives are the preferred substrates for the deubiquitinating activity of the PLpro. With k(cat)/K(M) of 602,000 M(-1)s(-1), PLpro hydrolyzes IS  ...[more]

Similar Datasets

| S-EPMC4875570 | biostudies-literature
| S-EPMC9094096 | biostudies-literature
| S-EPMC7161584 | biostudies-literature
| S-EPMC4403493 | biostudies-literature
| S-EPMC7605552 | biostudies-literature
| S-EPMC5896749 | biostudies-literature
| S-EPMC8423903 | biostudies-literature
| S-EPMC4031219 | biostudies-literature
| S-EPMC8103894 | biostudies-literature
| S-EPMC8983325 | biostudies-literature