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Biophysical Characterization Of Macromolecules

Biophysical Characterization Of Macromolecules
大分子的生物物理表征
批准号：
7967861
负责人：
PETER SCHUCK
金额：
$14.93万
依托单位：
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
依托单位国家：
美国
项目类别：
财政年份：
--
资助国家：
美国
项目状态：
未结题
起止时间：
至
来源：
https://reporter.nih.gov/project-details/7967861
关键词：
Adaptor Signaling ProteinBiologicalBiosensing TechniquesCalmodulinCircular Dichroism SpectroscopyDifferential Scanning CalorimetryEnzymesExtracellular DomainField Flow FractionationGlutamate ReceptorGoalsLaboratoriesMembrane ProteinsMethodologyMonoclonal AntibodiesPeptidesProteinsResearchSignal TransductionSurface Plasmon ResonanceSystemT-Cell ActivationTechniquesTitrationsToll-like receptorsTubulinViral Proteinsanalytical ultracentrifugationanthrax edema factorexperiencehuman RORA proteinlight scatteringmacromoleculemicrocalorimetrynew technologyparticle

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英文摘要
Experimental techniques employed are analytical ultracentrifugation, static and dynamic light scattering, field flow fractionation, isothermal titration microcalorimetry, differential scanning calorimetry, circular dichroism spectroscopy, and surface plasmon resonance biosensing. Molecules studied in this project include MHC-like viral proteins, extracellular domains of glutamate receptors, adaptor proteins involved in the formation of signaling particles after T-cell activation, the enzyme ROR-alpha, the adaptor protein TIRAP of the Toll-like receptor and MyD88, the anthrax edema factor interaction with calmodulin and a monoclonal antibody, tubulin, and peptides derived from malarial surface proteins.
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BIOPHYSICAL CHARACTERIZATION OF MACROMOLECULES
Dynamics of Protein Assemblies by Analytical Ultracentrifugation
Multi-Method Approaches for the Study of Complex Protein Interactions
Multi-Method Approaches for the Study of Complex Protein Interactions
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