MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
批准号:
6699400
负责人:
ERKANG FAN
金额:
$30.18万
依托单位:
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:
2000-02-01 至 2006-01-31
关键词:
Escherichia coliVibrio choleraechemical modelschemical synthesischolera toxincombinatorial chemistryenterotoxinsenzyme linked immunosorbent assayexperimental designsintermolecular interactionligandsmolecular shapeprotein structure functionreceptor bindingsolutionsstoichiometrythermodynamicsthermostability
中文摘要
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英文摘要
The goal of this proposal is to take advantage of the structural symmetry of multimeric proteins, a rarely explored property, to arrive eventually at structurally complementary multidentate protein ligands with ultra-high affinity and specificity. The long term objective is to illuminate an area of fundamental biological interest: the molecular recognition properties of multidentate protein ligands and the use of such ligands to control protein functions. Specifically, this proposal encompasses the design, synthesis and evaluation of multidentate ligands targeting a pair of ideal model systems: the heat-labile enterotoxin from E. coli (LT) and the closely related cholera toxin secreted by V. cholerae (CT), which are both AB5 heterohexamers. The biological mechanism of the actions of LT and CT includes a critical step of receptor recognition on the target cell by the B pentamer. The five-fold symmetry of the B subunits of LT and CT offers good opportunities to develop pentadentate ligands with overall structures complementary to the arrangement of toxin receptor binding sites. Such ligands will be created stepwise using a modular approach with each module providing opportunities for further optimization Building on the principles of molecular recognition, our proposed work will combine the powers of combinatorial chemistry and structure-based design to arrive at ultrahigh affinity pentadentate ligands. The affinity of the ligands obtained will be investigated with a variety of analytical tools. Detailed thermodynamics of ligand-protein interaction will be studied using a series of mono- to penta-dentate ligands. The proposed research has broad implications for the field of molecular recognition in general since it is at the frontiers of investigations focusing on multidentate ligands interacting with multimeric proteins. In addition, high affinity ligands derived from our work have potential health benefits, as they may lead to the development of agents useful for the detection, treatment, and prevention of AB5 toxin-related enterotoxigenic diseases.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
Solid-phase and solution-phase syntheses of oligomeric guanidines bearing peptide side chains.
带有肽侧链的寡聚胍的固相和溶液相合成。
DOI:
10.1021/jo051226t
发表时间:
2005
期刊:
The Journal of organic chemistry.
影响因子:
--
作者:
[Zhang,Zhongsheng, Fan,Erkang]
通讯作者:
Fan,Erkang
Modular synthesis and study of multivalent carbohydrate ligands with long and flexible linkers.
具有长而灵活的连接体的多价碳水化合物配体的模块化合成和研究。
DOI:
10.1016/s0076-6879(03)01014-0
发表时间:
2003
期刊:
Methods in enzymology.
影响因子:
--
作者:
[Zhang,Zhongsheng, Fan,Erkang]
通讯作者:
Fan,Erkang
MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
-
批准号:6497140
-
项目类别:
-
资助金额:$28.46万
-
财政年份:2000
-
负责人:ERKANG FAN
-
依托单位:
MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
-
批准号:6627895
-
项目类别:
-
资助金额:$29.31万
-
财政年份:2000
-
负责人:ERKANG FAN
-
依托单位:
MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
-
批准号:6349894
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项目类别:
-
资助金额:$28.14万
-
财政年份:2000
-
负责人:ERKANG FAN
-
依托单位:
MULTIDENTATE HIGH AFFINITY LIGANDS FOR AB5 TOXINS
-
批准号:6045337
-
项目类别:
-
资助金额:$27.35万
-
财政年份:2000
-
负责人:ERKANG FAN
-
依托单位:
CATALYTIC ANTIBODIES--SELECTIVE AMIDE BOND HYDROLYSIS
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批准号:2171497
-
项目类别:
-
资助金额:$2.86万
-
财政年份:1995
-
负责人:ERKANG FAN
-
依托单位:
CATALYTIC ANTIBODIES--SELECTIVE AMIDE BOND HYDROLYSIS
-
批准号:2171496
-
项目类别:
-
资助金额:$2.37万
-
财政年份:1994
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负责人:ERKANG FAN
-
依托单位:
海外基金