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DESCRIPTION (provided by applicant): Adrenal ascorbate-dependent cytochrome (cyt.) b561 is a transmembrane electron transporter required for synthesis of catecholamine and some peptide hormone and is the prototype of an expanding and insufficiently characterized cyt. b561 protein family; other mammalian family members have been linked to intestinal iron transport and tumor suppression. Our overall goal is to characterize the mechanism of adrenal b561 and to use information about this cytochrome to understand the structure and function of other b561 family members. The specific aims of this project are: 1) Define the structural kernel of adrenal cyt. b561, determine its relationship to the membrane bilayer, and evaluate the kernel's generality among mammalian cyt. b561 family members; 2) Characterize the interaction of adrenal cyt. b561 with its natural reductant, ascorbate, and its natural oxidant, semidehydroascorbate; and 3) Determine the path of electron flow via adrenal cyt. b561 and its regulation. Planned experiments will be conducted on the native mammalian protein and recombinant wild type and mutant forms of the adrenal cytochrome and other mammalian cyt. b561 family members in prokaryotic and eukaryotic systems that we have developed. We will characterize the topological, structural, and kinetic properties of these recombinant proteins and purified endogenous adrenal cyt b561 using biochemical and biophysical techniques. Understanding how adrenal cyt. b561 functions is a fundamental part of understanding the physiology and pathology of epinephrine and norepinephrine and of some peptide hormones in humans. Defining similarities and differences between adrenal cyt. b561 and recently-discovered human cyt. b561 family members will accelerate characterization of the physiological and pathological roles of the newer cyt. b561s.
期刊论文(8)
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会议论文
Electrochemical reduction of ferrous alpha-verdoheme in complex with heme oxygenase-1.
亚铁 α-绿血红素与血红素加氧酶-1 复合物的电化学还原。
DOI: 10.1016/j.jinorgbio.2007.05.016
发表时间: 2007
期刊: Journal of inorganic biochemistry
影响因子: 3.9
作者: [Sato,Hideaki, Higashimoto,Yuichiro, Sakamoto,Hiroshi, Sugishima,Masakazu, Takahashi,Kenichi, Palmer,Graham, Noguchi,Masato]
通讯作者: Noguchi,Masato
Spectroscopic evidence of the role of an axial ligand histidinate in the mechanism of adrenal cytochrome b(561).
轴向配体组氨酸在肾上腺细胞色素 b(561) 机制中作用的光谱证据。
DOI: 10.1021/bi301127k
发表时间: 2012
期刊: Biochemistry
影响因子: 2.9
作者: [daSilva,GiordanoFZ, Shinkarev,VladimirP, Kamensky,YuryA, Palmer,Graham]
通讯作者: Palmer,Graham
DOI: 10.1021/bi401078b
发表时间: 2014-06-10
期刊: BIOCHEMISTRY
影响因子: 2.9
作者: [Jancura, Daniel, Stanicova, Jana, Palmer, Graham, Fabian, Marian]
通讯作者: Fabian, Marian
High-yield production, purification and characterization of functional human duodenal cytochrome b in an Escherichia coli system.
在大肠杆菌系统中高产生产、纯化和表征功能性人十二指肠细胞色素 b。
DOI: 10.1016/j.pep.2011.04.001
发表时间: 2011
期刊: Protein expression and purification
影响因子: 1.6
作者: [Liu,Wen, Wu,Gang, Tsai,Ah-Lim, Kulmacz,RichardJ]
通讯作者: Kulmacz,RichardJ
Structure and function of cytochrome b561
  • 批准号:
    7246408
  • 项目类别:
  • 资助金额:
    $29.15万
  • 财政年份:
    2007
  • 负责人:
    Graham A. Palmer
  • 依托单位:
Structure and function of cytochrome b561
  • 批准号:
    7585163
  • 项目类别:
  • 资助金额:
    $28.4万
  • 财政年份:
    2007
  • 负责人:
    Graham A. Palmer
  • 依托单位:
Structure and function of cytochrome b561
  • 批准号:
    7393110
  • 项目类别:
  • 资助金额:
    $28.4万
  • 财政年份:
    2007
  • 负责人:
    Graham A. Palmer
  • 依托单位:
CATALYTIC MECHANISM OF HEME/COPPER OXIDASES
  • 批准号:
    2599775
  • 项目类别:
  • 资助金额:
    $15.58万
  • 财政年份:
    1998
  • 负责人:
    Graham A. Palmer
  • 依托单位:
海外基金