MICROFOCUS X-RAY DATA COLLECTION WITH DIFFRACTION-CAPABLE MICROFLUIDIC CHIPS
MICROFOCUS X-RAY DATA COLLECTION WITH DIFFRACTION-CAPABLE MICROFLUIDIC CHIPS
批准号:
7955162
负责人:
JAMES BERGER
金额:
$1.93万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-04-01 至 2010-03-31
关键词:
BiologicalComplexComputer Retrieval of Information on Scientific Projects DatabaseCrystallizationDNADNA biosynthesisData CollectionFundingGrantIn SituInstitutionMembrane ProteinsMicrofluidicsMolecular ConformationResearchResearch PersonnelResourcesRoentgen RaysSamplingSourceStructureSystemUnited States National Institutes of HealthVirulence Factorsbeamlinecryogenicsdesigninterestmacromolecular assemblymolecular assembly/self assemblyresearch studystructural biology
中文摘要
这个子项目是众多研究子项目之一
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Microfocus X-ray Data Collection with Diffraction-Capable Microfluidic Chips and Microcrystals of Large Molecular Assemblies
We have recently developed microfluidic crystallization chips designed for in-situ diffraction data collection. These chips have been designed for low-volume crystallization experiments (10nl sample per sample chamber) and to minimize x-ray background scatter from the chip material. Sections can be removed from chips, cryoprotectants can be added, and cryogenic data collection is possible. Crystals grown in these chips are typically small (40x40x40 ¿m) and data collection from them will benefit from the use of microfocus X-ray sources to further reduce background X-ray scatter. This subproject aims to demonstrate the utility of the NE-CAT microfocus X-ray beamline for data collection from microfluidic chips and determine structures of samples of broad biological interest including DNA replication complexes, membrane proteins and bacterial virulence factors.
We also have been studying large macromolecular assemblies that remodel and replicate DNA. Many of these systems assume multiple conformational states during their catalytic cycle, making them challenging structural targets, and prone to forming microcrystals despite extensive optimization efforts.
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