CHARACTERIZATION OF NOVEL LCP MATRICES FOR MEMBRANE PROTEIN CRYSTALLIZATION BY S
CHARACTERIZATION OF NOVEL LCP MATRICES FOR MEMBRANE PROTEIN CRYSTALLIZATION BY S
批准号:
8362309
负责人:
Vadim Cherezov
金额:
$0.52万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-03-01 至 2012-02-29
关键词:
ArchitectureBehaviorCrystallizationDetergentsFundingG-Protein-Coupled ReceptorsGrantHumanIn SituJointsLipidsMeasuresMembrane ProteinsNational Center for Research ResourcesPhasePreparationPrincipal InvestigatorPropertyProteinsRadiationResearchResearch InfrastructureResolutionResourcesSamplingSourceTechniquesTechnologyUnited States National Institutes of HealthWorkbeamlinecostdesigninnovationnovelresearch studystructural biology
中文摘要
点击翻译按钮获取中文摘要
英文摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
Structural studies of membrane proteins are limited by the availability of crystals diffracting to high resolution. Crystallization in lipidic cubic phase (LCP) matrices (or in meso) has proven to yield high quality crystals of challenging membrane proteins, such as human G protein-coupled receptors. Broader applications of in meso techniques require identification of new lipids with specific phase properties capable of stabilizing proteins with large range of sizes and architectures. At the Joint Center for Innovative Membrane Protein Technologies (JCIMPT) we are working on design and synthesis of such lipids. The phase and structural behavior of novel lipid matrices should be thoroughly characterized prior to being used in specific applications. We propose to overcome the obstacles associated with conventional preparation of lipid samples for x-ray studies, by preparing samples in 96-well sandwich plates and measuring them in situ at the BioSAXS beamline. This approach will allow us to screen for effects of detergents, additive lipids, proteins as well as great variety of precipitants on the lipidic matrices in the high-throughput mode at conditions mimicking those encountered during crystallization trials. During the duration of this proposal we anticipate to fully characterize 10-12 most promising novel lipids pre-selected out of a larger pool of synthesized candidates. The obtained results will be indispensable for selection of proper lipids and guiding in meso crystallization experiments.
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