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A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay.

A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Research Abstract Details 

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  • A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Abstract Text:

    daniel a p gutmannDaniel A P Gutmann,eiichi mizohataEiichi Mizohata,simon newsteadSimon Newstead,sebastian ferrandonSebastian Ferrandon,vincent postisVincent Postis,xiaobing xiaXiaobing Xia,peter j f hendersonPeter J F Henderson,hendrik w van veenHendrik W van Veen,bernadette byrneBernadette Byrne,

    One key to successful crystallization of membrane proteins is the identification of detergents that maintain the protein in a soluble, monodispersed state. Because of their hydrophobic nature, membrane proteins are particularly prone to forming insoluble aggregates over time. This nonspecific aggregation of the molecules reduces the likelihood of the regular association of the protein molecules essential for crystal lattice formation. Critical buffer components affecting the aggregation of membrane proteins include detergent choice, salt concentration, and presence of glycerol. The optimization of these parameters is often a time- and protein-consuming process. Here we describe a novel ultracentrifugation dispersity sedimentation (UDS) assay in which ultracentrifugation of very small (5 microL) volumes of purified, soluble membrane protein is combined with SDS-PAGE analysis to rapidly assess the degree of protein aggregation. The results from the UDS method correlate very well with established methods like size-exclusion chromatography (SEC), while consuming considerably less protein. In addition, the UDS method allows rapid screening of detergents for membrane protein crystallization in a fraction of the time required by SEC. Here we use the UDS method in the identification of suitable detergents and buffer compositions for the crystallization of three recombinant prokaryotic membrane proteins. The implications of our results for membrane protein crystallization prescreening are discussed.

    A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Publishing Authors By Initials

    da gutmannDA Gutmann,e mizohataE Mizohata,s newsteadS Newstead,s ferrandonS Ferrandon,v postisV Postis,x xiaX Xia,pj hendersonPJ Henderson,hw van veenHW van Veen,b byrneB Byrne,

    For similar investigative techniques: centrifugation: ultracentrifugation research abstracts see: investigative techniques: centrifugation: ultracentrifugation research

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    A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Protein science : a publication of the Protein Soc

    VOLUME: 16

    Page Numbers: 1422-8

    Journal Abbreviation: Protein Sci.

    ISSN: 0961-8368

    DAY: 13

    MONTH: 06

    YEAR: 2007

    A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9211750

    A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Keywords Mesh Terms:

    KEYWORDS: Ultracentrifugation

    MESH TERMS: methods

    Chemical & Substance for Abstract: A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay. Information

    Substance Name: Membrane Proteins

    Registry Number: 0

    Grant and Affiliation Information for A high-throughput method for membrane protein solubility screening: the ultracentrifugation dispersity sedimentation assay.

    AFFILIATION: Membrane Protein Crystallography Group, Division of Molecular Biosciences, Imperial College London, UK.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Protein Sci

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