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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...

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Detalles Bibliográficos
Autores principales: Carpenter, Elisabeth P, Beis, Konstantinos, Cameron, Alexander D, Iwata, So
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science 2008
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.
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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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