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The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a phy...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592820/ https://www.ncbi.nlm.nih.gov/pubmed/19029339 http://dx.doi.org/10.1083/jcb.200808122 |
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author | Skinner, John J. Wood, Stacey Shorter, James Englander, S. Walter Black, Ben E. |
author_facet | Skinner, John J. Wood, Stacey Shorter, James Englander, S. Walter Black, Ben E. |
author_sort | Skinner, John J. |
collection | PubMed |
description | The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a physiologically relevant time scale by a self–self interaction between its two forms, culminating in a large pool of active Mad2. Recent structural, biochemical, and cell biological advances suggest that the catalyzed conversion of Mad2 requires a major structural rearrangement that transits through a partially unfolded intermediate. |
format | Text |
id | pubmed-2592820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25928202009-06-01 The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching Skinner, John J. Wood, Stacey Shorter, James Englander, S. Walter Black, Ben E. J Cell Biol Reviews The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a physiologically relevant time scale by a self–self interaction between its two forms, culminating in a large pool of active Mad2. Recent structural, biochemical, and cell biological advances suggest that the catalyzed conversion of Mad2 requires a major structural rearrangement that transits through a partially unfolded intermediate. The Rockefeller University Press 2008-12-01 /pmc/articles/PMC2592820/ /pubmed/19029339 http://dx.doi.org/10.1083/jcb.200808122 Text en © 2008 Skinner et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Skinner, John J. Wood, Stacey Shorter, James Englander, S. Walter Black, Ben E. The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title | The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title_full | The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title_fullStr | The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title_full_unstemmed | The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title_short | The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching |
title_sort | mad2 partial unfolding model: regulating mitosis through mad2 conformational switching |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592820/ https://www.ncbi.nlm.nih.gov/pubmed/19029339 http://dx.doi.org/10.1083/jcb.200808122 |
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