MAPPING THE IGF-II BINDING SITE OF THE IGF-II RECEPTOR
MAPPING THE IGF-II BINDING SITE OF THE IGF-II RECEPTOR
批准号:
2143616
负责人:
RICHARD G. MACDONALD
金额:
$12.51万
依托单位国家:
美国
项目类别:
财政年份:
1994
资助国家:
美国
项目状态:
已结题
起止时间:
1994-01-01 至 1996-12-31
关键词:
SDS polyacrylamide gel electrophoresis animal genetic material tag chemical binding chimeric proteins complementary DNA crosslink genetic library genetic mapping growth factor receptors high performance liquid chromatography insulinlike growth factor molecular cloning nucleic acid sequence protein sequence protein structure function receptor binding receptor coupling receptor expression site directed mutagenesis tissue /cell culture
中文摘要
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英文摘要
The insulin-like growth factor II (IGF-II) receptor has high affinity
binding sites for the polypeptide IGF-II and glycosylated lysosomal
enzymes. This unique receptor's key role in transporting lysosomal enzymes
is well established, but the mechanism by which IGF-II-initiated signal
transduction events are mediated by the IGF-II receptor is controversial.
To help elucidate this mechanism, the objective of this project is to map
the ICF-II binding site of the IGF-II receptor using two complementary
approaches. First, purified 125I-IGF-II affinity-labelled receptors will
be digested with endoproteinase Glu-C, then peptide regions of the
receptor covalently attached to IGF-II will be isolated for sequencing.
Second, cDNA clones encoding the IGF-II receptor's avian homolog, which
does not bind ICF-II, will be isolated by screening chicken cDNA libraries
with radiolabelled fragments of mammalian IGF-II receptor cDNAs. Sequence
and mapping information as well as reagents obtained in those studies will
be used to designate targets for site-directed mutagenesis of the
mammalian receptor's IGF-II binding site and to design avian/mammalian
receptor chimeras. Wild-type, mutant and chimeric receptors will be
expressed in mammalian cells to assess IGF-II binding parameters, and to
investigate structure-function relationships linking IGF-II binding to
signal transduction.
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IGF-II-Based Approach to Therapy for Pancreatic Cancer
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批准号:9110216
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项目类别:
-
资助金额:$19.57万
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财政年份:2015
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负责人:RICHARD G. MACDONALD
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依托单位:
Molecular Dissection of IGF2R Growth Suppressor Activity
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批准号:6515149
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项目类别:
-
资助金额:$16.54万
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财政年份:2001
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负责人:RICHARD G. MACDONALD
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依托单位:
Molecular Dissection of IGF2R Growth Suppressor Activity
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批准号:6634068
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项目类别:
-
资助金额:$16.54万
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财政年份:2001
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负责人:RICHARD G. MACDONALD
-
依托单位:
Molecular Dissection of IGF2R Growth Suppressor Activity
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批准号:6359218
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项目类别:
-
资助金额:$16.25万
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财政年份:2001
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负责人:RICHARD G. MACDONALD
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依托单位:
Molecular Dissection of IGF2R Growth Suppressor Activity
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批准号:6767546
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项目类别:
-
资助金额:$16.54万
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财政年份:2001
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负责人:RICHARD G. MACDONALD
-
依托单位:
MAPPING THE IGF II BINDING SITE OF THE IGF II RECEPTOR
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批准号:2143619
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项目类别:
-
资助金额:$2.61万
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财政年份:1996
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负责人:RICHARD G. MACDONALD
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依托单位:
MAPPING THE IGF-II BINDING SITE OF THE IGF-II RECEPTOR
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批准号:2143617
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项目类别:
-
资助金额:$2.46万
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财政年份:1995
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负责人:RICHARD G. MACDONALD
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依托单位:
MAPPING THE IGF-II BINDING SITE OF THE IGF-II RECEPTOR
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批准号:2143615
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项目类别:
-
资助金额:$12.64万
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财政年份:1994
-
负责人:RICHARD G. MACDONALD
-
依托单位:
MAPPING THE IGF-II BINDING SITE OF THE IGF-II RECEPTOR
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批准号:2143618
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项目类别:
-
资助金额:$13.07万
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财政年份:1994
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负责人:RICHARD G. MACDONALD
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依托单位:
BIOSYNTHESIS AND PROCESSING OF THE IGF-II RECEPTOR
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批准号:3446013
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项目类别:
-
资助金额:$5.79万
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财政年份:1984
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负责人:RICHARD G. MACDONALD
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依托单位:
BIOSYNTHESIS AND PROCESSING OF THE IGF-II RECEPTOR
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批准号:3447273
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项目类别:
-
资助金额:$6.15万
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财政年份:1984
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负责人:RICHARD G. MACDONALD
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依托单位: