G PROTEIN STRUCTURE/FUNCTION
G PROTEIN STRUCTURE/FUNCTION
批准号:
2019887
负责人:
HEIDI E HAMM
金额:
$24.79万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-07-01 至 2002-06-30
关键词:
Escherichia coli G protein Sf9 cell line biological signal transduction chimeric proteins enzyme activity guanine nucleotide exchange factors guanosine diphosphate guanosinetriphosphatases intermolecular interaction protein structure function receptor binding receptor coupling receptor expression receptor mediated endocytosis rhodopsin site directed mutagenesis
中文摘要
描述(研究者摘要):生物转导
英文摘要
DESCRIPTION (Investigator's Abstract): The transduction of biological
signals such as light, hormones and neurotransmitters starts by a specific
interaction of the ligand or stimulus with a receptor protein. The ultimate
cell-specific responses are produced via receptor activation of specific
GTP-binding proteins. While the functional aspects of this process are
well-defined, the structural basis of G protein function, the regulated
interactions between receptor, G protein and effector, and the activation
processes are understood only partially. In the last grant period,
expression systems for generation of large amounts of wild type and mutant G
proteins were worked out. In addition, the three-dimensional structures of
alpha and beta/gamma subunits, and heterotrimeric alpha/beta/gamma complex
were solved in collaboration with Paul Sigler's laboratory. This structural
information, in conjunction with functional studies, suggests detailed
hypotheses for the mechanisms that keep G proteins inactive in the absence
of activated receptors, that lead to serial activation of G proteins and
effectors by activated receptors during signal transduction, and that
determine the timing of the active state by controlling GTP hydrolysis
rates. These hypotheses will be tested in this proposal, using
site-directed mutagenesis and heterologous expression of G protein alpha and
beta/gamma subunits in E. coli and Baculovirus-infected SF9 cells. The
model systems include a variety of receptors, G proteins and effectors,
either native or overexpressed, tested in biochemical assays in
reconstituted membranes. The critical amino acid residues involved in these
processes will be determined. The collaboration with Sigler's laboratory
will continue with crystallization and resolution of structures of
receptor-G protein complexes and complexes of G protein alpha and beta/gamma
subunits with a number of downstream effectors. The combined structural and
functional information will contribute to our understanding of basic
mechanisms of cellular activation by a variety of signals, and will also
provide insight into diseases that affect G protein function.
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海外基金