LOCAL AND LONG RANGE INTERACTIONS IN PROTEIN FOLDING
LOCAL AND LONG RANGE INTERACTIONS IN PROTEIN FOLDING
批准号:
6625097
负责人:
J. MARTIN SCHOLTZ
金额:
$20.16万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-05-01 至 2004-11-30
中文摘要
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英文摘要
DESCRIPTION: A complete description of protein folding and stability remains as
one of the most important questions in modern biochemistry. To realize the full
potential of Dr. Scholtz's growing knowledge of genome information, he must
come to an understanding of the rules for protein folding. This proposal
addresses some very fundamental issues in protein stability and folding ranging
from the role of electrostatic interactions in defining the folded and unfolded
conformations of proteins to the role that interactions between networks of
polar residues have on the rate of protein folding, the stability of the final
folded structure and the mechanism of folding. Dr. Scholtz's basic approach is
to make quantitative comparisons between different proteins or variants that
alter a specific property. These comparisons encompass global structural and
stability measurements to detailed atomic level descriptions of interactions to
kinetic studies on the folding reactions. A complete molecular and quantitative
description of the rules for protein folding will only be achieved through
studies such as those presented here.
This proposal addresses two major topics in protein folding and stability: 1)
What are the roles of electrostatic interactions in defining the structure and
stability of the folded and unfolded conformations of a protein, and 2) How do
complex networks of interactions between polar groups govern the stability and
folding of globular proteins? Dr. Scholtz will use a variety of different
experimental techniques to explore the molecular forces responsible for protein
stability, folding and structure. The strength of the program is the use of
comparisons-comparisons between single-site variants of proteins, between
proteins and model peptides and between the properties of a protein under
different solution conditions. This broad-based comparative approach will allow
the PI to reach a better understanding of the rules for protein folding,
stability and structure and these rules will help answer these very basic
questions in molecular medicine.
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Texas A&M University Interdisciplinary Life Sciences Building Build-Out
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批准号:7839650
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项目类别:
-
资助金额:$352.96万
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财政年份:2010
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负责人:J. MARTIN SCHOLTZ
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依托单位:
HIERARCHY OF PROTEIN FOLDING AND STABILITY
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批准号:2191527
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项目类别:
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资助金额:$9.5万
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财政年份:1995
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负责人:J. MARTIN SCHOLTZ
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依托单位:
HIERARCHY OF PROTEIN FOLDING AND STABILITY
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批准号:2191528
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项目类别:
-
资助金额:$9.4万
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财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
HIERARCHY OF PROTEIN FOLDING AND STABILITY
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批准号:2910179
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项目类别:
-
资助金额:$11.07万
-
财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
LOCAL AND LONG RANGE INTERACTIONS IN PROTEIN FOLDING
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批准号:6283805
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项目类别:
-
资助金额:$20.16万
-
财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
LOCAL AND LONG RANGE INTERACTIONS IN PROTEIN FOLDING
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批准号:6476550
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项目类别:
-
资助金额:$20.16万
-
财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
HIERARCHY OF PROTEIN FOLDING AND STABILITY
-
批准号:2701672
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项目类别:
-
资助金额:$10.61万
-
财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
HIERARCHY OF PROTEIN FOLDING AND STABILITY
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批准号:2415306
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项目类别:
-
资助金额:$10.18万
-
财政年份:1995
-
负责人:J. MARTIN SCHOLTZ
-
依托单位:
LOCAL AND LONG RANGE INTERACTIONS IN PROTEIN FOLDING
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批准号:6679486
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项目类别:
-
资助金额:$20.16万
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财政年份:1995
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负责人:J. MARTIN SCHOLTZ
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依托单位:
FOLDING AND STABILITY OF APOMYOGLOBIN
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批准号:3044598
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项目类别:
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资助金额:$1.43万
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财政年份:1991
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负责人:J. MARTIN SCHOLTZ
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依托单位:
FOLDING AND STABILITY OF APOMYOGLOBIN
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批准号:3044599
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项目类别:
-
资助金额:$2.1万
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财政年份:1990
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负责人:J. MARTIN SCHOLTZ
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依托单位:
FOLDING AND STABILITY OF APOMYOGLOBIN
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批准号:3044597
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项目类别:
-
资助金额:$2.0万
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财政年份:1990
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负责人:J. MARTIN SCHOLTZ
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依托单位:
海外基金