STRUCTURE OF THE SODIUM PUMP NUCLEOTIDE BINDING DOMAIN
STRUCTURE OF THE SODIUM PUMP NUCLEOTIDE BINDING DOMAIN
批准号:
6163484
负责人:
CRAIG GATTO
金额:
$12.14万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-08-01 至 2003-07-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: (Verbatim from the Applicant's Abstract) The sodium pump has been
the target for the therapeutic treatment of congestive heart failure with
cardiac glycosides for more than a century. Unfortunately there is still little
known about the mechanism of cardiac glycoside inhibition. Experimental studies
over the past three decades have established some relationships between the
biochemical reactions catalyzed by the sodium pump and the transport reactions
it mediates. However, the molecular mechanisms by which the hydrolysis of ATP
is coupled to the "uphill" movement of ions remains a mystery. This probably
stems from the fact that there remains little known about the
structure-function relationship of this protein. Our long term goal is to gain
a complete understanding of the sodium pump transport mechanism which will
require high-resolution x-ray diffraction patterns of the enzyme in its various
conformations and the identification of specific amino acids residues
associated with ligand binding. However, the techniques required to get quality
crystals of membrane proteins have not yet been perfected. The specific
experiments outlined in this proposal will exploit bacterial genetics to
overexpress the large cytoplasmic loop of the Na,K-ATPase (Aim I). All the
residues thus far implicated in ATP binding and hydrolysis have been found in
this section of the protein. The same holds true for all members of this
important protein family (i.e., P-type ATPases). The ATP binding
characteristics of the wild type and mutant ATP binding domains will be
determined and structurally characterized using CD and x-ray crystallographic
techniques (Aim III). In addition, we will determine which other sections of
the Na,K-ATPase physically interact with the ATP binding domain (Aim II). The
results from this work will provide a map of the amino acids involved in ATP
coordination and thus help elucidate the coupling mechanism between ATP
hydrolysis and cation transport. The sodium pump is vital in a variety of
organs for fluid and electrolyte balance. These processes are in a dynamic
equilibrium and this equilibrium can become disrupted in a variety of disease
states. Before an adequate description of these pathological situations can be
made, a more complete understanding of sodium pump function is required.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Role for Na,K-ATPase in Nucleoplasmic Calcium Homeostasis
-
批准号:7895864
-
项目类别:
-
资助金额:$18.43万
-
财政年份:2009
-
负责人:CRAIG GATTO
-
依托单位:
Role for Na,K-ATPase in Nucleoplasmic Calcium Homeostasis
-
批准号:7674984
-
项目类别:
-
资助金额:$19.18万
-
财政年份:2009
-
负责人:CRAIG GATTO
-
依托单位:
Cell Structure-Function of Na pump Assembly
-
批准号:6848900
-
项目类别:
-
资助金额:$21.0万
-
财政年份:2000
-
负责人:CRAIG GATTO
-
依托单位:
Cell Physiology of Na,K-ATPase
-
批准号:8878545
-
项目类别:
-
资助金额:$34.8万
-
财政年份:2000
-
负责人:CRAIG GATTO
-
依托单位:
Cell Structure-Function of Na pump Assembly
-
批准号:8043852
-
项目类别:
-
资助金额:$33.12万
-
财政年份:2000
-
负责人:CRAIG GATTO
-
依托单位:
STRUCTURE OF THE SODIUM PUMP NUCLEOTIDE BINDING DOMAIN
-
批准号:6589622
-
项目类别:
-
资助金额:$2.69万
-
财政年份:2000
-
负责人:CRAIG GATTO
-
依托单位:
STRUCTURE/FUNCTION OF NA+/K+ ATPASE ATP BINDING DOMAIN
-
批准号:2901013
-
项目类别:
-
资助金额:$3.24万
-
财政年份:1999
-
负责人:CRAIG GATTO
-
依托单位:
STRUCTURE/FUNCTION OF NA+/K+ ATPASE ATP BINDING DOMAIN
-
批准号:2639836
-
项目类别:
-
资助金额:$3.15万
-
财政年份:1998
-
负责人:CRAIG GATTO
-
依托单位:
海外基金