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中文摘要
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英文摘要
The development of new biophysical techniques is of paramount importance to the advancement of science. This proposal aims to advance existing spectroscopic imaging techniques to elucidate the understanding of cellular membranes and to further this understanding by developing both new model systems and techniques with unprecedented chemical and spatial resolution for application to biological systems. A Raman near fleld scanning optical microscope (NSOM) was developed during the K99 phase that will enable vibrational spectroscopic imaging with nanoscale spatial resolution. Vibrational spectroscopic imaging offers the opportunity to spatially resolve biological systems solely on the basis ofthe molecules present. This enables the study of the dynamical and organizational characteristics of cells and tissue without the need for external labels, which can disrupt the behavior of the system. This proposal aims to further develop and apply these new techniques to elucidate further the characteristics of biomolecules located within cellular membranes. Specifically, model systems will be utilized to explore the biophysical insights gained from this new methodology. Planar supported bilayers will be used as a model system for domain formation motifs, particularly the chemical composition and interactions that are found in lipid domains. l\/Iore sophisticated model systems, such as confined vesicles, will be developed that will facilitate the ultimate goal of observing and understanding membrane heterogeneity and its role in cellular membrane processes such as signaling, and transport across the cell membrane. Ultimately, this proposal will utilize the established instrumentation and advance the methodology to gain insight into intact cell membranes. While domains are commonly ambiguously implicated in cell membrane processes related to pathogen infection, transport, and protein receptor activity, this research will demonstrate and clarify these molecular interactions at levels previously unattainable.
期刊论文(9)
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会议论文
DOI: 10.1039/c1an15432j
发表时间: 2011-11-07
期刊: The Analyst
影响因子: --
作者: [Asiala SM, Schultz ZD]
通讯作者: Schultz ZD
DOI: 10.1021/la301976s
发表时间: 2012-08-14
期刊: Langmuir : the ACS journal of surfaces and colloids
影响因子: --
作者: [Marr JM, Li F, Petlick AR, Schafer R, Hwang CT, Chabot A, Ruggiero ST, Tanner CE, Schultz ZD]
通讯作者: Schultz ZD
DOI: 10.1021/ac301739k
发表时间: 2012-09-04
期刊: ANALYTICAL CHEMISTRY
影响因子: 7.4
作者: [Alexander, Kristen D., Schultz, Zachary D.]
通讯作者: Schultz, Zachary D.
DOI: 10.1071/ch11019
发表时间: 2011-05-01
期刊: Australian journal of chemistry
影响因子: 1.1
作者: [Schultz ZD]
通讯作者: Schultz ZD
9
    Glycosylation Analysis by Sheath-Flow SERS
    • 批准号:
      10312126
    • 项目类别:
    • 资助金额:
      $19.2万
    • 财政年份:
      2021
    • 负责人:
      Zachary Schultz
    • 依托单位:
    Online Raman Diagnostics of Oncometabolites
    • 批准号:
      9675692
    • 项目类别:
    • 资助金额:
      $23.21万
    • 财政年份:
      2016
    • 负责人:
      Zachary Schultz
    • 依托单位:
    Online Raman Diagnostics of Oncometabolites
    • 批准号:
      9147682
    • 项目类别:
    • 资助金额:
      $36.39万
    • 财政年份:
      2016
    • 负责人:
      Zachary Schultz
    • 依托单位:
    Enhanced Raman Imaging of Ligand-Receptor Recognition
    • 批准号:
      10687237
    • 项目类别:
    • 资助金额:
      $33.35万
    • 财政年份:
      2015
    • 负责人:
      Zachary Schultz
    • 依托单位: