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DESCRIPTION (provided by applicant): PROJECT SUMMARY: The "nearest-neighbor recognition" (NNR) method is a promising chemical technique that provides fundamental insight into the lateral organization of fluid phospholipid membranes. In essence, NNR measurements take molecular-level snapshots of membrane organization by detecting and quantifying the tendency of lipids to become nearest-neighbors. The specific aims of this research are to use the NNR method to investigate lipid-peptide interactions, lipid-protein interactions, and lipid-lipid interactions in the presence of natural and unnatural membrane-perturbing agents. More specifically, lipid-peptide experiments will be part of a long-term effort aimed at clarifying the "rules" governing the sorting of peripheral and integral proteins by lipids in fluid bilayers. Lipid-protein studies, in combination with transbilayer phospholipid interactions, will provide insight into a much-debated issue that has a direct bearing on the structure and function of cell membranes-an issue for which there is virtually no experimental data; that is, the "communication" between the inner and outer leaflets of lipid bilayers. Finally, the effects of selected general anesthetics and amyloid beta-peptides on lipid-lipid interactions will provide fundamental insight into two problems that have major biomedical importance; that is, the mechanism by which general anesthetics function, and the molecular basis of Alzheimer's disease. The long-term objective of this program is to develop a fundamental understanding of the two-dimensional organization of fluid bilayers, which will help bring exploitable targets in biological membranes into sharper focus. Such insight will assist the rational design of novel classes of therapeutic agents. RELEVANCE: Cell membranes are "the skin" of cells, which are essential for maintaining the living state. Understanding how these membranes are organized in two dimensions, at the molecular level, should aid in the design of new and improved drugs; e.g., drugs that can be used to cure Alzheimer's disease, drugs to combat alcohol abuse, and drugs that can be used as improved general anesthetics. This program is aimed at obtaining such an understanding using simple model systems.
期刊论文(25)
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会议论文
Detection of unusual lipid mixing in cholesterol-rich phospholipid bilayers: the long and the short of it.
检测富含胆固醇的磷脂双层中的异常脂质混合:其长和短。
DOI: 10.1021/ja0359355
发表时间: 2003
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Tokutake,Nobuya, Jing,Bingwen, Regen,StevenL]
通讯作者: Regen,StevenL
DOI: 10.1021/la100878s
发表时间: 2010-04-20
期刊: LANGMUIR
影响因子: 3.9
作者: [Janout, Vaclav, Turkyilmaz, Serhan, Regen, Steven L.]
通讯作者: Regen, Steven L.
Selective sterol-phospholipid associations in fluid bilayers.
流体双层中的选择性甾醇-磷脂结合。
DOI: 10.1021/ja017269i
发表时间: 2002
期刊: Journal of the American Chemical Society
影响因子: 15
作者: [Sugahara,Michihiro, Uragami,Maki, Regen,StevenL]
通讯作者: Regen,StevenL
Cholesterol-phospholipid association in fluid bilayers: a thermodynamic analysis from nearest-neighbor recognition measurements.
流体双层中的胆固醇-磷脂关联:最近邻识别测量的热力学分析。
DOI: 10.1529/biophysj.106.084152
发表时间: 2006
期刊: Biophysical journal.
影响因子: --
作者: [Zhang,Jianbing, Cao,Honghua, Jing,Bingwen, Almeida,PauloF, Regen,StevenL]
通讯作者: Regen,StevenL
18
    Molecular Umbrella-Amphotericin B Conjugates
    • 批准号:
      8516063
    • 项目类别:
    • 资助金额:
      $31.61万
    • 财政年份:
      2012
    • 负责人:
      STEVEN L. REGEN
    • 依托单位:
    Molecular Umbrella-Amphotericin B Conjugates
    • 批准号:
      8666555
    • 项目类别:
    • 资助金额:
      $31.23万
    • 财政年份:
      2012
    • 负责人:
      STEVEN L. REGEN
    • 依托单位:
    Molecular Umbrella-Amphotericin B Conjugates
    • 批准号:
      8370193
    • 项目类别:
    • 资助金额:
      $28.18万
    • 财政年份:
      2012
    • 负责人:
      STEVEN L. REGEN
    • 依托单位:
    MOBILITY STUDY OF ALLYLAMINE BY FRAP
    • 批准号:
      7598453
    • 项目类别:
    • 资助金额:
      $0.32万
    • 财政年份:
      2007
    • 负责人:
      STEVEN L. REGEN
    • 依托单位: