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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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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