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Overcoming the challenges of membrane protein crystallography
Membrane protein structural biology is still a largely unconquered area, given that approximately 25% of all proteins are membrane proteins and yet less than 150 unique structures are available. Membrane proteins have proven to be difficult to study owing to their partially hydrophobic surfaces, fle...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2580798/ https://www.ncbi.nlm.nih.gov/pubmed/18674618 http://dx.doi.org/10.1016/j.sbi.2008.07.001 |
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author | Carpenter, Elisabeth P Beis, Konstantinos Cameron, Alexander D Iwata, So |
author_facet | Carpenter, Elisabeth P Beis, Konstantinos Cameron, Alexander D Iwata, So |
author_sort | Carpenter, Elisabeth P |
collection | PubMed |
description | Membrane protein structural biology is still a largely unconquered area, given that approximately 25% of all proteins are membrane proteins and yet less than 150 unique structures are available. Membrane proteins have proven to be difficult to study owing to their partially hydrophobic surfaces, flexibility and lack of stability. The field is now taking advantage of the high-throughput revolution in structural biology and methods are emerging for effective expression, solubilisation, purification and crystallisation of membrane proteins. These technical advances will lead to a rapid increase in the rate at which membrane protein structures are solved in the near future. |
format | Text |
id | pubmed-2580798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25807982008-11-14 Overcoming the challenges of membrane protein crystallography Carpenter, Elisabeth P Beis, Konstantinos Cameron, Alexander D Iwata, So Curr Opin Struct Biol Article Membrane protein structural biology is still a largely unconquered area, given that approximately 25% of all proteins are membrane proteins and yet less than 150 unique structures are available. Membrane proteins have proven to be difficult to study owing to their partially hydrophobic surfaces, flexibility and lack of stability. The field is now taking advantage of the high-throughput revolution in structural biology and methods are emerging for effective expression, solubilisation, purification and crystallisation of membrane proteins. These technical advances will lead to a rapid increase in the rate at which membrane protein structures are solved in the near future. Elsevier Science 2008-10 /pmc/articles/PMC2580798/ /pubmed/18674618 http://dx.doi.org/10.1016/j.sbi.2008.07.001 Text en © 2008 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Carpenter, Elisabeth P Beis, Konstantinos Cameron, Alexander D Iwata, So Overcoming the challenges of membrane protein crystallography |
title | Overcoming the challenges of membrane protein crystallography |
title_full | Overcoming the challenges of membrane protein crystallography |
title_fullStr | Overcoming the challenges of membrane protein crystallography |
title_full_unstemmed | Overcoming the challenges of membrane protein crystallography |
title_short | Overcoming the challenges of membrane protein crystallography |
title_sort | overcoming the challenges of membrane protein crystallography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2580798/ https://www.ncbi.nlm.nih.gov/pubmed/18674618 http://dx.doi.org/10.1016/j.sbi.2008.07.001 |
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