Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.

The nucleocapsid protein (N) and the phosphoprotein (P) of nonsegmented negative-strand (NNS) RNA viruses interact with each other to accomplish two crucial events necessary for the viral replication cycle. First, the P protein binds to the aggregation prone nascent N molecules maintaining them in a...

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Main Authors: Arindam Mondal, Arunava Roy, Sandipto Sarkar, Jishnu Mukherjee, Tridib Ganguly, Dhrubajyoti Chattopadhyay
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3317646?pdf=render
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spelling doaj-8d406dcae44f4c5cbef97e55338293772020-11-25T01:47:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0174e3462310.1371/journal.pone.0034623Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.Arindam MondalArunava RoySandipto SarkarJishnu MukherjeeTridib GangulyDhrubajyoti ChattopadhyayThe nucleocapsid protein (N) and the phosphoprotein (P) of nonsegmented negative-strand (NNS) RNA viruses interact with each other to accomplish two crucial events necessary for the viral replication cycle. First, the P protein binds to the aggregation prone nascent N molecules maintaining them in a soluble monomeric (N(0)) form (N(0)-P complex). It is this form that is competent for specific encapsidation of the viral genome. Second, the P protein binds to oligomeric N in the nucleoprotein complex (N-RNA-P complex), and thereby facilitates the recruitment of the viral polymerase (L) onto its template. All previous attempts to study these complexes relied on co-expression of the two proteins in diverse systems. In this study, we have characterised these different modes of N-P interaction in detail and for the first time have been able to reconstitute these complexes individually in vitro in the chandipura virus (CHPV), a human pathogenic NNS RNA virus. Using a battery of truncated mutants of the N protein, we have been able to identify two mutually exclusive domains of N involved in differential interaction with the P protein. An unique N-terminal binding site, comprising of amino acids (aa) 1-180 form the N(0)-P interacting region, whereas, C-terminal residues spanning aa 320-390 is instrumental in N-RNA-P interactions. Significantly, the ex-vivo data also supports these observations. Based on these results, we suggest that the P protein acts as N-specific chaperone and thereby partially masking the N-N self-association region, which leads to the specific recognition of viral genome RNA by N(0).http://europepmc.org/articles/PMC3317646?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Arindam Mondal
Arunava Roy
Sandipto Sarkar
Jishnu Mukherjee
Tridib Ganguly
Dhrubajyoti Chattopadhyay
spellingShingle Arindam Mondal
Arunava Roy
Sandipto Sarkar
Jishnu Mukherjee
Tridib Ganguly
Dhrubajyoti Chattopadhyay
Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
PLoS ONE
author_facet Arindam Mondal
Arunava Roy
Sandipto Sarkar
Jishnu Mukherjee
Tridib Ganguly
Dhrubajyoti Chattopadhyay
author_sort Arindam Mondal
title Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
title_short Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
title_full Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
title_fullStr Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
title_full_unstemmed Interaction of chandipura virus N and P proteins: identification of two mutually exclusive domains of N involved in interaction with P.
title_sort interaction of chandipura virus n and p proteins: identification of two mutually exclusive domains of n involved in interaction with p.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The nucleocapsid protein (N) and the phosphoprotein (P) of nonsegmented negative-strand (NNS) RNA viruses interact with each other to accomplish two crucial events necessary for the viral replication cycle. First, the P protein binds to the aggregation prone nascent N molecules maintaining them in a soluble monomeric (N(0)) form (N(0)-P complex). It is this form that is competent for specific encapsidation of the viral genome. Second, the P protein binds to oligomeric N in the nucleoprotein complex (N-RNA-P complex), and thereby facilitates the recruitment of the viral polymerase (L) onto its template. All previous attempts to study these complexes relied on co-expression of the two proteins in diverse systems. In this study, we have characterised these different modes of N-P interaction in detail and for the first time have been able to reconstitute these complexes individually in vitro in the chandipura virus (CHPV), a human pathogenic NNS RNA virus. Using a battery of truncated mutants of the N protein, we have been able to identify two mutually exclusive domains of N involved in differential interaction with the P protein. An unique N-terminal binding site, comprising of amino acids (aa) 1-180 form the N(0)-P interacting region, whereas, C-terminal residues spanning aa 320-390 is instrumental in N-RNA-P interactions. Significantly, the ex-vivo data also supports these observations. Based on these results, we suggest that the P protein acts as N-specific chaperone and thereby partially masking the N-N self-association region, which leads to the specific recognition of viral genome RNA by N(0).
url http://europepmc.org/articles/PMC3317646?pdf=render
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