SYNTHESIS OF DOPA-MODIFIED PEG

多巴修饰 PEG 的合成

基本信息

  • 批准号:
    8361231
  • 负责人:
  • 金额:
    --
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2011
  • 资助国家:
    美国
  • 起止时间:
    2011-03-01 至 2012-02-29
  • 项目状态:
    已结题

项目摘要

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Marine mussels are known to anchor themselves to underwater surfaces in turbulent intertidal zones. They secrete adhesive proteins that can rapidly cure to form adhesive plaques. It is believed that 3,4-dihydroxyphenylalanine (DOPA), an amino acid found in MAPs at a content as much as 25 mol%, is responsible for both strong interfacial binding and curing of these proteins. The goals of our research are to combine the water-resistant adhesive characteristics of DOPA and its derivatives with biocompatible, synthetic polymer for different biomedical applications. One aspect of our research is to design DOPA-modified polymers for the use as tissue adhesive or sealant, which exploits DOPA's ability to cure rapidly and to adhere to a wide variety of surfaces in an aqueous environment. Through the use of different synthetic polymers, it is possible to create novel bioadhesives with improved characteristics (i.e. water-resistant adhesion, biodegradability, and safety) as compared to existing medical adhesives. Another research area focuses on combining DOPA with antifouling polymers to create coating materials that can repel proteins, cells, and bacteria. These coatings can render different surfaces resistant to cell and bacteria adhesion ranging from metals, semiconductors, and synthetic polymers.
这个子项目是利用这些资源的众多研究子项目之一

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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John R. Murphy其他文献

THE METABOLISM OF VARIOUSLY LABELED GLUCOSE IN RAT LIVER IN VIVO
  • DOI:
    10.1016/s0021-9258(18)64989-0
  • 发表时间:
    1957-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    John A. Muntz;John R. Murphy
  • 通讯作者:
    John R. Murphy
Identification of the primary metal ion-activation sites of the diphtheria tox represser by X-ray crystallography and site-directed mutational analysis
通过 X 射线晶体学和定点突变分析鉴定白喉毒素抑制剂的主要金属离子激活位点
  • DOI:
  • 发表时间:
    1996
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Xiaochun Ding;Hui‐yan Zeng;N. Schiering;Dagmar Ringe;John R. Murphy
  • 通讯作者:
    John R. Murphy
THE METABOLISM OF GLUCOSE IN THE PERFUSED RAT LIVER
  • DOI:
    10.1016/s0021-9258(18)64990-7
  • 发表时间:
    1957-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    John R. Murphy;John A. Muntz
  • 通讯作者:
    John A. Muntz
CHAPTER 4 – Modifying Specific Properties: Mechanical Properties – Fillers
第 4 章 – 修改特定属性:机械属性 – 填料
  • DOI:
    10.1016/b978-185617370-4/50006-3
  • 发表时间:
    2001
  • 期刊:
  • 影响因子:
    0
  • 作者:
    John R. Murphy
  • 通讯作者:
    John R. Murphy
CHAPTER 2 – Types of Additive and the Main Technical Trends
  • DOI:
    10.1016/b978-185617370-4/50004-x
  • 发表时间:
    2001
  • 期刊:
  • 影响因子:
    0
  • 作者:
    John R. Murphy
  • 通讯作者:
    John R. Murphy

John R. Murphy的其他文献

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{{ truncateString('John R. Murphy', 18)}}的其他基金

COPI interactions mediate toxin entry: a common shared mechanism of translocation
COPI 相互作用介导毒素进入:一种常见的易位共享机制
  • 批准号:
    8375448
  • 财政年份:
    2012
  • 资助金额:
    --
  • 项目类别:
SYNTHESIS OF NOVEL MATERIALS BASED ON MUSSEL ADHESIVE PROTEINS
基于贻贝粘附蛋白的新材料的合成
  • 批准号:
    8361232
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
COPI interactions mediate toxin entry: a common shared mechanism of translocation
COPI 相互作用介导毒素进入:一种常见的易位共享机制
  • 批准号:
    8233433
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
TRAINING IN THE USE OF BRUKER AND VARIAN SPECTROMETERS AND NMR
布鲁克和瓦里安光谱仪和核磁共振的使用培训
  • 批准号:
    8361233
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
Biomolecule Core
生物分子核心
  • 批准号:
    8307624
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
MUSSEL ADHESIVE PROTEINS
贻贝粘附蛋白
  • 批准号:
    8361230
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
COPI interactions mediate toxin entry: a common shared mechanism of translocation
COPI 相互作用介导毒素进入:一种常见的易位共享机制
  • 批准号:
    7669764
  • 财政年份:
    2009
  • 资助金额:
    --
  • 项目类别:
Administration Core
行政核心
  • 批准号:
    8443485
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
Community Relations Core
社区关系核心
  • 批准号:
    8443481
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
ID OF CYTOSOLIC TRANSLOCATION FACTORS INVOLVED IN BACTERIAL INTOXIFICATION
细菌中毒相关细胞质转位因子的识别
  • 批准号:
    7369220
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:

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I-Corps: Translation Potential of Peptidic Ensembles as Novel Bio-adhesives
I-Corps:肽整体作为新型生物粘合剂的转化潜力
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