Dual Oxidases (Duox): Enzymology & Biological Function
Dual Oxidases (Duox): Enzymology & Biological Function
批准号:
7057319
负责人:
John David Lambeth
金额:
$26.12万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-05-01 至 2008-04-30
关键词:
DrosophilidaeNAD(P)H dehydrogenasebiological modelscalciumcell membraneclinical researchcrosslinkenzyme activityenzyme mechanismenzyme structureepitheliumextracellular matrixhormone biosynthesishuman genetic material taghuman tissueimmunityimmunofluorescence techniqueiodotyrosinemass spectrometryoxidationperoxidasesprotein localizationthyroid hormonestissue /cell culturetyrosine
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): A family of Dual Oxidases (Duox) has been defined. Duox enzymes consist of three domains: 1) an NADPH-oxidase domain homologous to gp91phox, the catalytic subunit of the phagocyte respiratory burst oxidase; 2) a calcium-binding domain; and 3) a peroxidase domain. Located in plasma membrane of epithelial cells (colon, lung, thyroid, pancreas), Duoxs' are proposed to function by using intracellular NADPH to reduce 02 to form H202 outside the cell. The latter is used by the peroxidase domain to catalyze peroxidative reactions involving modification of extracellular matrix proteins and probably other extracellular small molecules. Specifically, Duox's are proposed to function biologically in innate immunity, endocrine function and cancer. We identified and cloned two human isoforms, h-Duox1 and h-Duox2, and have identified Duox enzymes in diverse species, including C. elegans and Drosophila. In C. elegans, we showed that the enzyme functions to chemically cross-link tyrosine residues in collagen and other extracellular matrix proteins, thus stabilizing the structure of the cuticle. We will test the hypothesis that a general function of Duox enzymes throughout the animal kingdom is the chemical modification of tyrosine and/or other residues of extracellular matrix. Genetic and biochemical methods will be used to test this hypothesis in Drosophila, where we propose that the tyrosine modifications stabilize the structure of the wing. Phage display methods will be used to develop peptide inhibitors of the peroxidase domains of h-Duoxl and h-Duox2, and these will be used to investigate normal biological functions of Duox such as thyroid hormone biosynthesis and innate immunity. Enzymatic properties and regulation by calcium of Duox will be documented, and the transmembrane topology of the domains will be explored. These studies will provide for the first time fundamental information regarding the enzymology, topology and biological functions of this newly discovered group of enzymes and will document their ability to chemically modify extracellular matrix (ECM). Because ECM is a critical determinant of transformation Duox enzymes may play an important role in cancer biology in some tissues.
期刊论文(7)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1186/1471-2148-7-178
发表时间:
2007-09-27
期刊:
BMC EVOLUTIONARY BIOLOGY
影响因子:
3.4
作者:
[Kawahara, Tsukasa, Lambeth, J. David]
通讯作者:
Lambeth, J. David
DOI:
10.1186/1471-2148-7-109
发表时间:
2007-07-06
期刊:
BMC evolutionary biology
影响因子:
3.4
作者:
[Kawahara T, Quinn MT, Lambeth JD]
通讯作者:
Lambeth JD
NOX1 and NOX2 as Therapeutic Targets in Influenza
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批准号:8889190
-
项目类别:
-
资助金额:$45.96万
-
财政年份:2012
-
负责人:John David Lambeth
-
依托单位:
NOX1 and NOX2 as Therapeutic Targets in Influenza
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批准号:8490301
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项目类别:
-
资助金额:$22.54万
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财政年份:2012
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负责人:John David Lambeth
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依托单位:
NOX1 and NOX2 as Therapeutic Targets in Influenza
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批准号:8390976
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项目类别:
-
资助金额:$19.28万
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财政年份:2012
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负责人:John David Lambeth
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依托单位:
Project 4: NOX1 Involvement In Colon Cancer
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批准号:8099689
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项目类别:
-
资助金额:$13.83万
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财政年份:2010
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负责人:John David Lambeth
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依托单位:
Mox 1: A Novel Mitogenic Oxidase
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批准号:7811391
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项目类别:
-
资助金额:$64.33万
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财政年份:2009
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负责人:John David Lambeth
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依托单位:
Project 4: NOX1 Involvement In Colon Cancer
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批准号:7511070
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项目类别:
-
资助金额:$13.57万
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财政年份:2008
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负责人:John David Lambeth
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依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:8066381
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项目类别:
-
资助金额:$24.55万
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财政年份:2004
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负责人:John David Lambeth
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依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:7069094
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项目类别:
-
资助金额:$24.5万
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财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:7419032
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项目类别:
-
资助金额:$23.79万
-
财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:7239651
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项目类别:
-
资助金额:$23.79万
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财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:6817762
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项目类别:
-
资助金额:$25.09万
-
财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:8449706
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项目类别:
-
资助金额:$23.08万
-
财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:7887135
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项目类别:
-
资助金额:$25.31万
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财政年份:2004
-
负责人:John David Lambeth
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依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:8247071
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项目类别:
-
资助金额:$24.55万
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财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:8658004
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项目类别:
-
资助金额:$23.81万
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财政年份:2004
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负责人:John David Lambeth
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依托单位:
Regulation of Nox Enzymes by Calcium and Novel Subunits
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批准号:6913621
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项目类别:
-
资助金额:$25.09万
-
财政年份:2004
-
负责人:John David Lambeth
-
依托单位:
Dual Oxidases (Duox): Enzymology & Biological Function
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批准号:6891403
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项目类别:
-
资助金额:$26.75万
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财政年份:2003
-
负责人:John David Lambeth
-
依托单位:
Dual Oxidases (Duox): Enzymology & Biological Function
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批准号:6742511
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项目类别:
-
资助金额:$26.75万
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财政年份:2003
-
负责人:John David Lambeth
-
依托单位:
Dual Oxidases (Duox): Enzymology & Biological Function
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批准号:6594087
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项目类别:
-
资助金额:$26.75万
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财政年份:2003
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负责人:John David Lambeth
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依托单位:
MOX 1--A NOVEL MITOGENIC OXIDASE
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批准号:6038184
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项目类别:
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资助金额:$25.46万
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财政年份:2000
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负责人:John David Lambeth
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依托单位:
海外基金