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Insights into integrin-ligand binding and activation from the first crystal structure
CHAPTER SUMMARY: Integrin receptors transduce bidirectional signals between extracellular adhesion molecules and intracellular cytoskeletal and signalling molecules. The structural basis of integrin signalling is unknown, but the recent publication of the first crystal structure of the extracellular...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240139/ https://www.ncbi.nlm.nih.gov/pubmed/12110125 http://dx.doi.org/10.1186/ar563 |
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author | Humphries, Martin J |
author_facet | Humphries, Martin J |
author_sort | Humphries, Martin J |
collection | PubMed |
description | CHAPTER SUMMARY: Integrin receptors transduce bidirectional signals between extracellular adhesion molecules and intracellular cytoskeletal and signalling molecules. The structural basis of integrin signalling is unknown, but the recent publication of the first crystal structure of the extracellular domain of integrin αVβ3 has provided a number of insights. In this review, previous structure–function analyses of integrins that have employed biochemical and molecular biological approaches are placed in the context of the crystal structure, and novel routes to the development of integrin antagonists are discussed. |
format | Online Article Text |
id | pubmed-3240139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32401392011-12-16 Insights into integrin-ligand binding and activation from the first crystal structure Humphries, Martin J Arthritis Res Review CHAPTER SUMMARY: Integrin receptors transduce bidirectional signals between extracellular adhesion molecules and intracellular cytoskeletal and signalling molecules. The structural basis of integrin signalling is unknown, but the recent publication of the first crystal structure of the extracellular domain of integrin αVβ3 has provided a number of insights. In this review, previous structure–function analyses of integrins that have employed biochemical and molecular biological approaches are placed in the context of the crystal structure, and novel routes to the development of integrin antagonists are discussed. BioMed Central 2002 2002-05-09 /pmc/articles/PMC3240139/ /pubmed/12110125 http://dx.doi.org/10.1186/ar563 Text en Copyright ©2002 BioMed Central Ltd |
spellingShingle | Review Humphries, Martin J Insights into integrin-ligand binding and activation from the first crystal structure |
title | Insights into integrin-ligand binding and activation from the first crystal structure |
title_full | Insights into integrin-ligand binding and activation from the first crystal structure |
title_fullStr | Insights into integrin-ligand binding and activation from the first crystal structure |
title_full_unstemmed | Insights into integrin-ligand binding and activation from the first crystal structure |
title_short | Insights into integrin-ligand binding and activation from the first crystal structure |
title_sort | insights into integrin-ligand binding and activation from the first crystal structure |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3240139/ https://www.ncbi.nlm.nih.gov/pubmed/12110125 http://dx.doi.org/10.1186/ar563 |
work_keys_str_mv | AT humphriesmartinj insightsintointegrinligandbindingandactivationfromthefirstcrystalstructure |