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DESCRIPTION (provided by applicant): The past two decades have witnessed significant advances in the analysis of complex biological environments. Fluorescence imaging utilizing indicator dyes or proteins has played an important role but also suffers from significant limitations including toxicity, chemical stability and perturbation of the system. Though quite useful for a variety of ions and small molecules where fluorescent indicators or ionophores are available, large categories of chemically and biologically relevant analytes elude detection due to a lack of suitable indicators or lack of intrinsic optical or electrochemical activity. The use of membrane receptors, ion channels and molecular transporters in chemical sensing applications presents several potential advantages over traditional reporters as many such membrane proteins are highly selective to small molecule and/or protein based ligands and typically demonstrate high affinity binding that may translate to high sensitivity of the sensor. Here we propose a new class of nanometer-sized, biomimetic chemical sensors with embedded membrane proteins for intracellular, in vivo and environmental labeling, tracing and sensing applications. To realize such a sensor platform, we will create phospholipid vesicles from a series of lipids that can be chemically crosslinked and we will functionalize the vesicles with reconstituted membrane proteins. The key features of our sensor platform are: a) a phospholipid membrane formed from self assembly of polymerizable lipids and lipid composites; b) incorporated biological signal transduction elements, e.g. receptors; c) external membrane elements that serve to initiate cellular uptake and localization of the sensor; and d) indicator or reporter elements that serve to generate an optical signal. This modular sensor geometry will provide a general platform that can be utilized to readily design a wide variety of sensors.
期刊论文(8)
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Analysis of protein kinase A activity in insulin-secreting cells using a cell-penetrating protein substrate and capillary electrophoresis.
使用细胞穿透蛋白底物和毛细管电泳分析胰岛素分泌细胞中的蛋白激酶 A 活性。
DOI: 10.1007/s00216-010-3776-7
发表时间: 2010
期刊: Analytical and bioanalytical chemistry
影响因子: 4.3
作者: [Rauf,Femina, Huang,Yiding, Muhandiramlage,ThusithaP, Aspinwall,CraigA]
通讯作者: Aspinwall,CraigA
DOI: 10.1007/s00216-014-8246-1
发表时间: 2015-01
期刊: ANALYTICAL AND BIOANALYTICAL CHEMISTRY
影响因子: 4.3
作者: [Li, Zhen, Muhandiramlage, Thusitha P., Keogh, John P., Hall, Henry K., Jr., Aspinwall, Craig A.]
通讯作者: Aspinwall, Craig A.
Polymer-stabilized phospholipid vesicles with a controllable, pH-dependent disassembly mechanism.
聚合物稳定的磷脂囊泡,具有可控、pH 依赖性分解机制。
DOI: 10.1021/la803358m
发表时间: 2009
期刊: Langmuir : the ACS journal of surfaces and colloids
影响因子: --
作者: [Roberts,DavidL, Ma,Yaning, Bowles,StevenE, Janczak,ColleenM, Pyun,Jeffrey, Saavedra,SScott, Aspinwall,CraigA]
通讯作者: Aspinwall,CraigA
Nanoshell sensors for cellular analysis
  • 批准号:
    9149291
  • 项目类别:
  • 资助金额:
    $29.67万
  • 财政年份:
    2015
  • 负责人:
    CRAIG A ASPINWALL
  • 依托单位:
Nanoshell sensors for cellular analysis
  • 批准号:
    9307921
  • 项目类别:
  • 资助金额:
    $29.67万
  • 财政年份:
    2015
  • 负责人:
    CRAIG A ASPINWALL
  • 依托单位:
Nanoshell sensors for cellular analysis
  • 批准号:
    9006016
  • 项目类别:
  • 资助金额:
    $29.58万
  • 财政年份:
    2015
  • 负责人:
    CRAIG A ASPINWALL
  • 依托单位:
Hybrid nanomaterials for dynamic, intracellular radioisotope detection
  • 批准号:
    8854082
  • 项目类别:
  • 资助金额:
    $18.46万
  • 财政年份:
    2014
  • 负责人:
    CRAIG A ASPINWALL
  • 依托单位:
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