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Libraries of Uniquely Folded Alpha-Helical Proteins

Libraries of Uniquely Folded Alpha-Helical Proteins
独特折叠的α螺旋蛋白质文库
批准号:
6725369
负责人:
MICHAEL H HECHT
金额:
$23.34万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-04-01 至 2006-03-31

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中文摘要
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英文摘要
DESCRIPTION: The overall goal of the proposed research is to design and produce libraries of de novo proteins that fold into well ordered alpha-helical structures. This goal will be pursued through an approach that uses both rational design and combinatorial methods. The first step will entail the design of a new structural scaffold specifying a uniquely folded 4-helix bundle. Each sequence position will be defined to occur in a particular environment in the desired alpha-helical structure (exposed vs. buried; alpha-helix vs. turn etc.). The second step will use combinatorial methods to generate a library of de novo amino acid sequences consistent with the designed scaffold. The combinatorial diversity will not be random, but instead, will be designed to deliver at each position only those amino acids most compatible with the structural environment of that position in the scaffold. The specific aims of this project are (1) to design a new structural scaffold that specifies a 4-helix bundle; (2) to design and construct a library of synthetic genes that encode a large collection of protein sequences consistent with this new scaffold; (3) to express and purify de novo proteins from this collection; (4) to biophysically characterize the structural and thermodynamic properties of the purified proteins and thereby assess whether they form molten globule ensembles or uniquely folded structures; and (5) to determine the 3-dimensional structures of representative proteins by NMR spectroscopy. The ability to design and construct large collections of uniquely folded de novo proteins will have a significant impact on biotechnology and medicine. Whereas current applications of biotechnology typically focus on the control, modification, and production of naturally occurring genes and proteins, future applications will not be limited to macromolecules provided by nature. The ability to produce libraries of well folded de novo proteins is an initial and essential step towards the ultimate goal of discovering novel proteins "tailor made" for applications in industry and medicine.
期刊论文(11)
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DOI: 10.1385/1-59745-116-9:53
发表时间: 2006
期刊: Methods in molecular biology
影响因子: --
作者: [L. H. Bradley;P. Thumfort;M. Hecht]
通讯作者: L. H. Bradley;P. Thumfort;M. Hecht
DOI: 10.1021/sb200018e
发表时间: 2012-04-20
期刊: ACS SYNTHETIC BIOLOGY
影响因子: 4.7
作者: [Cherny, Izhack, Korolev, Maria, Koehler, Angela N., Hecht, Michael H.]
通讯作者: Hecht, Michael H.
Protein design by binary patterning of polar and nonpolar amino acids.
通过极性和非极性氨基酸的二元模式进行蛋白质设计。
DOI: 10.1385/1-59745-187-8:155
发表时间: 2007
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Bradley,LukeH, Wei,Yinan, Thumfort,Peter, Wurth,Christine, Hecht,MichaelH]
通讯作者: Hecht,MichaelH
A High Throughput Screen for Inhibitors of Aggregation of the Alzheimer's Peptide
  • 批准号:
    7390351
  • 项目类别:
  • 资助金额:
    $16.45万
  • 财政年份:
    2007
  • 负责人:
    MICHAEL H HECHT
  • 依托单位:
A High Throughput Screen for Inhibitors of Aggregation of the Alzheimer's Peptide
  • 批准号:
    7256597
  • 项目类别:
  • 资助金额:
    $20.15万
  • 财政年份:
    2007
  • 负责人:
    MICHAEL H HECHT
  • 依托单位:
Libraries of Uniquely Folded Alpha-Helical Proteins
  • 批准号:
    6636606
  • 项目类别:
  • 资助金额:
    $23.41万
  • 财政年份:
    2001
  • 负责人:
    MICHAEL H HECHT
  • 依托单位:
Libraries of Uniquely Folded Alpha-Helical Proteins
  • 批准号:
    6318449
  • 项目类别:
  • 资助金额:
    $23.34万
  • 财政年份:
    2001
  • 负责人:
    MICHAEL H HECHT
  • 依托单位:
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