课题基金 / 基金详情

SYNTHESIS OF NOVEL IRON & MIXED METAL-SULFUR CLUSTERS

SYNTHESIS OF NOVEL IRON & MIXED METAL-SULFUR CLUSTERS
新型铁的合成
批准号:
3299727
负责人:
JEAN LE GALL
金额:
$14.16万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-12-01 至 1993-11-30

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中文摘要
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英文摘要
Iron is the most common transition metal found in proteins and participates in many fundamental physiological functions in all living organisms, in particular in processes related to energy conservation. Among the iron-containing structures which are common to eucaryotes as well as procaryotes, iron-sulfur clusters are extremely important, not only because of their ubiquity, but also because of their unique redox properties. The mechanisms of incorporation and stabilization of iron into these structures is still far from being well understood. Anerobic bacteria, which are important to man in disease and in health, constitute an excellent source of iron-sulfur cluster containing proteins and, as such, are ideal tools for their study. The long term objective of this research project is to understand the conversion mechanisms between three and four iron-containing clusters found in certain ferredoxins and their significance for the regulation of electron flow in multiple electron transfer chains. The use of ferredoxins and artificially reconceived polypeptides as templates for the synthesis of new mixed-metal clusters will also be explored as a means to develop new molecules and examine their potential catalytic properties. Specific aims of this research are: 1) to prepare new mixed-metal clusters incorporated into Desulfovibrio gigas ferredoxin II (a Co-Fe and a Zn-Fe cluster have already been obtained from this protein; 2) to search for other ferredoxins that could perform better than the D. gigas protein in the synthesis of these new metal clusters; 3) to prepare specifically isotope-labelled, either 57 Fe or 56 Fe iron-sulfur clusters and investigate their properties using different spectrometric techniques; 4) to clone and express D. gigas ferredoxin gene in E. coli in order to over-produce the protein for physical studies and also to be able to perform site-directed mutagenesis to understand how 3Fe and 4Fe sulfur clusters are formed and stabilized; 5) to perform physiological experiments with the transformed mixed-metal clusters and the mutated proteins; 6) to extend these techniques to complex metal-containing enzymes; 7) to monitor the above experiments using modern computer graphics modeling.
期刊论文(28)
专著(0)
科研奖励(0)
会议论文
Molecular dynamics simulations of the cytochrome c3-rubredoxin complex from Desulfovibrio vulgaris.
普通脱硫弧菌细胞色素 c3-红氧还蛋白复合物的分子动力学模拟。
DOI: 10.1002/prot.340110207
发表时间: 1991
期刊: Proteins
影响因子: 2.9
作者: [Stewart,DE, Wampler,JE]
通讯作者: Wampler,JE
Computational chemistry and molecular modeling of electron-transfer proteins.
电子转移蛋白的计算化学和分子建模。
DOI: 10.1016/0076-6879(94)43042-x
发表时间: 1994
期刊: Methods in enzymology
影响因子: --
作者: [Wampler,JE]
通讯作者: Wampler,JE
DOI: 10.1016/s0005-2728(05)80270-1
发表时间: 1991
期刊: Biochimica et biophysica acta
影响因子: --
作者: [Moura,JJ, Costa,C, Liu,MY, Moura,I, LeGall,J]
通讯作者: LeGall,J
Isolation and characterization of flavoredoxin, a new flavoprotein that permits in vitro reconstitution of an electron transfer chain from molecular hydrogen to sulfite reduction in the bacterium Desulfovibrio gigas.
风味蛋白的分离和表征,风味蛋白是一种新的黄素蛋白,可在细菌脱硫弧菌中体外重建从分子氢到亚硫酸盐还原的电子传递链。
DOI: 10.1006/abbi.1993.1253
发表时间: 1993
期刊: Archives of biochemistry and biophysics
影响因子: 3.9
作者: [Chen,L, Liu,MY, LeGall,J]
通讯作者: LeGall,J
22
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      6180970
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