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TEMPLATE-DIRECTED SYNTHESIS--SEQUENCE SPECIFIC MATERIALS

TEMPLATE-DIRECTED SYNTHESIS--SEQUENCE SPECIFIC MATERIALS
模板指导合成——序列特定材料
批准号:
2772067
负责人:
DAVID Gilbert LYNN
金额:
$11.08万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-30 至 1999-08-31

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中文摘要
翻译
描述(改编自申请人的摘要):该过程
英文摘要
DESCRIPTION (Adapted from the applicant's abstract): The processes that enable the accurate flow of genetic information in biology, transcription of DNA into RNA, and translation into protein are template-directed polymerizations. Inspired by the Watson-Crick duplex structure of DNA, many attempts to emulate template-directed synthesis for the construction of sequence-specific and monodisperse materials have been reported; however, these attempts have had only limited success. A general method for accurate template-directed translation of an existing polymer could have as profound an effect on biomaterials research as the polymerase chain reaction (PCR) has had on biological and genome research. Employing the principles that drive these biological reactions, it has been possible to efficiently drive a ligation reaction as directed by a complementary template which shows the necessary accuracy to make oligomeric and polymeric materials. This proposal aims to demonstrate that it is possible to perform multiple coupling steps and accurately prepare complementary oligomeric materials from a polymeric template. Specifically, it is proposed to: 1) construct a novel amide-based template on which to control the reactions; 2) develop thermodynamically controlled conditions for imine coupling of designed monomers along the template; and 3) develop thermodynamically-controlled conditions for ring-opening metathesis polymerization of novel monomers to give sequence specific products. The demonstration of these general approaches could open new extensions of these and other reactions to the construction of specific oligomeric and polymeric biomaterials.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
Structure-function relationships in side chain lactam cross-linked peptide models of a conserved N-terminal domain of apolipoprotein E.
载脂蛋白 E 保守 N 末端结构域的侧链内酰胺交联肽模型中的结构-功能关系。
DOI: 10.1021/bi980482f
发表时间: 1998
期刊: Biochemistry.
影响因子: --
作者: [Benzinger,TL, Braddock,DT, Dominguez,SR, Burkoth,TS, Miller-Auer,H, Subramanian,RM, Fless,GM, Jones,DN, Lynn,DG, Meredith,SC]
通讯作者: Meredith,SC
Reading DNA differently.
以不同的方式读取 DNA。
DOI: 10.1002/(sici)1097-0282(1998)48:1
发表时间: 1998
期刊: Biopolymers.
影响因子: --
作者: [Gat,Y, Lynn,DG]
通讯作者: Lynn,DG
Faculty postion in computational protein design and evolution
  • 批准号:
    7860756
  • 项目类别:
  • 资助金额:
    $36.0万
  • 财政年份:
    2009
  • 负责人:
    DAVID Gilbert LYNN
  • 依托单位:
Faculty postion in computational protein design and evolution
  • 批准号:
    7943924
  • 项目类别:
  • 资助金额:
    $35.83万
  • 财政年份:
    2009
  • 负责人:
    DAVID Gilbert LYNN
  • 依托单位:
STUDY OF ZN BINDING SITE IN AMYLOID FIBRILS BY XAFS
  • 批准号:
    6975537
  • 项目类别:
  • 资助金额:
    $2.74万
  • 财政年份:
    2004
  • 负责人:
    DAVID Gilbert LYNN
  • 依托单位:
TEMPLATE-DIRECTED SYNTHESIS--SEQUENCE SPECIFIC MATERIALS
  • 批准号:
    2454244
  • 项目类别:
  • 资助金额:
    $11.08万
  • 财政年份:
    1997
  • 负责人:
    DAVID Gilbert LYNN
  • 依托单位:
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