MECHANISMS OF ARSENIC TRANSPORT AND BIOTRANSFORMATIONS
砷转运和生物转化机制
基本信息
- 批准号:9923901
- 负责人:
- 金额:$ 33.96万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-04-01 至 2025-03-31
- 项目状态:未结题
- 来源:
- 关键词:AcetyltransferaseAffectAntibioticsArsenicArsenicalsArsenitesBiochemicalBiochemistryBiologyBiosensing TechniquesBiosensorCancer EtiologyCardiovascular systemCategoriesChildhoodCrystallographyDevelopmental Delay DisordersDiabetes MellitusEnvironmental CarcinogensEnzymesFlowersFundingGene ProteinsGenesGoalsGrantHealthHeart DiseasesHerbicidesHumanHuman MicrobiomeLyaseMalignant NeoplasmsMalignant neoplasm of urinary bladderMetabolic BiotransformationMethylationMethyltransferaseMolecularMolecular GeneticsNational Institute of General Medical SciencesNatural ProductsOxidasesPathway interactionsPeripheral Vascular DiseasesPhysiologicalProteinsRecording of previous eventsRegulationResearchResistanceRoleSkin CancerStructureToxic Environmental SubstancesToxic effectToxinUnited StatesVisionantimicrobial drugenzyme structurefallshealth applicationmicrobial genomenervous system disordernovelpermeasepollutantprogramsresistance gene
项目摘要
Project Summary/Abstract: Arsenic is the most pervasive toxin, considered by the EPA to be one the
most significant potential environmental threats to human health. Arsenic exposure is a cause of cancer, heart
disease, childhood developmental delay, and disrupts the human microbiome. Our research program
blossomed during the current funding period of our NIGMS grant, focusing on arsenic transporters
and biotransformations, which modify its availability, speciation, mobility and toxicity. We are uniquely
qualified for this project: over the lifetime of this grant, my group identified and characterized the majority of
ars genes/proteins involved in arsenic transport, biotransformations and resistance and their impact on the
global arsenic biogeocycle. We discovered enzymes of the arsenic methylation cycle and elucidated
mechanisms and structures of the enzymes of biotransformation, developed biosensors for
organoarsenicals herbicides and discovered organoarsenicals with the potential to be novel antimicrobial
agents. My goals for the next five years fall into four categories. 1) Structure/function analysis of enzymes
of arsenic biotransformations. We will elucidate the catalytic cycle of the ArsM arsenite S-
adenosylmethione (SAM) methyltransferase, the ArsH methylarsenite oxidases, the ArsI C-As bond lyases
and the ArsN N-acetyltransferase through biochemical and structural analysis. 2) Regulation and biosensing.
We will determine the structural details of metalloregulation. We will devise new applications for sensing
environmental organoarsenical pollutants. 3) Arsenic transporters; we identified a number of new permeases
for organoarsenicals and will determine the mechanism of transport by a combination of molecular genetics,
biochemistry and crystallography. 4) Arsenical antibiotics; we recently identified two organoarsenical natural
products with antibiotic activity. We will determine the pathways of synthesis and mode of action of
these novel compounds and discover new natural products with potential health applications. My overall
vision is a research program of sufficient breadth to encompass identification of the physiological roles of
known arsenic resistance genes and sufficient depth to elucidate their molecular mechanisms. Microbial
genomes have many uncharacterized arsenic-related genes. There are predicted permeases and enzymes
with no known substrate or function. We predict these are involved in arsenical transport or biotransformations.
We will mine microbial genomes for new ars genes, deduce their evolutionary histories and determine how they
affect cycling of environmental arsenicals. We will discover their physiological functions. Their protein
products will be purified and characterized by biochemical and structural analyses. My overarching theme is
to make substantial contributions to understanding of the global arsenic biogeocycle and its impact on
human health.
项目摘要/摘要:砷是最普遍存在的毒素,被EPA认为是环境污染最严重的毒素之一
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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BARRY P. ROSEN其他文献
BARRY P. ROSEN的其他文献
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{{ truncateString('BARRY P. ROSEN', 18)}}的其他基金
MECHANISMS OF ARSENIC TRANSPORT AND BIOTRANSFORMATIONS
砷转运和生物转化机制
- 批准号:
10595533 - 财政年份:2020
- 资助金额:
$ 33.96万 - 项目类别:
MECHANISMS OF ARSENIC TRANSPORT AND BIOTRANSFORMATIONS
砷转运和生物转化机制
- 批准号:
10374036 - 财政年份:2020
- 资助金额:
$ 33.96万 - 项目类别:
XAS STUDIES OF NOVEL ARSENIC BINDING SITES IN AS(III)-RESPONSIVE TRANSCRIPTIONAL
AS(III) 响应转录中新型砷结合位点的 XAS 研究
- 批准号:
8170040 - 财政年份:2010
- 资助金额:
$ 33.96万 - 项目类别:
XAS STUDIES OF NOVEL ARSENIC BINDING SITES IN AS(III)-RESPONSIVE TRANSCRIPTIONAL
AS(III) 响应转录中新型砷结合位点的 XAS 研究
- 批准号:
7954364 - 财政年份:2009
- 资助金额:
$ 33.96万 - 项目类别:
XAS STUDIES OF NOVEL ARSENIC BINDING SITES IN AS (III)-RESPONSIVE TRANSCRIPTIONA
AS (III) 响应转录中新型砷结合位点的 XAS 研究
- 批准号:
7722025 - 财政年份:2008
- 资助金额:
$ 33.96万 - 项目类别:
XAS STUDIES OF NOVEL ARSENIC BINDING SITES IN AS (III)-RESPONSIVE TRANSCRIPTIONA
AS (III) 响应转录中新型砷结合位点的 XAS 研究
- 批准号:
7598285 - 财政年份:2007
- 资助金额:
$ 33.96万 - 项目类别:
THE ATP-COUPLED ARSENICAL PUMP OF ESCHERICHIA COLI
大肠杆菌的 ATP 耦合砷泵
- 批准号:
6395920 - 财政年份:2000
- 资助金额:
$ 33.96万 - 项目类别:
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