Bio-optical and Bio-electronic Materials for Real-time Analyte Detection

用于实时分析物检测的生物光学和生物电子材料

基本信息

  • 批准号:
    8054786
  • 负责人:
  • 金额:
    $ 22.71万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2001
  • 资助国家:
    美国
  • 起止时间:
    2001-05-01 至 2013-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Current methods for the detection of diagnostic proteins entail time- and resource-intensive immunochemical techniques that, even under ideal circumstances, require an hour or more to return an answer to the clinician's hands. This sluggish response fits poorly into the timeframe of modern healthcare, hindering patient compliance and, in some circumstances, the efficiency and safety with which drugs and procedures are administered. (Consider: a diagnostic test that returns an answer in less than 15 minutes differs qualitatively from a test that requires 30 minutes because the latter requires a second interaction with the clinician.) Here we propose the development of a rapid, point-of-care method for the simultaneous detection of multiple diagnostic proteins. Our approach, which utilizes electrochemistry to monitor the binding-induced folding of polypeptide- or protein-based recognition elements, will be rapid, specific, convenient and, critically, selective enough to employ directly in blood serum and -we propose- whole blood. And while our initial development efforts will focus on the detection of proteins diagnostic of HIV infection (such as anti-HIV antibodies), the approach will be general enough to be of use in the detection of a wide range of clinically relevant markers. The development of rapid, parallelizable point-of-care diagnostics could significantly impact the safety, compliance and efficacy of therapies and medical procedures ranging from the detection of infectious diseases, the treatment of autoimmune diseases, and the routine monitoring of health status. PUBLIC HEALTH RELEVANCE Here we proposed the development of a reagentless, electrochemical platform for the simultaneous detection of multiple proteins diagnostic of disease. The proposed technology will be rapid, specific, and selective enough to employ directly at the point of care, thus significantly improving the speed with which molecular diagnostics can be performed and their results acted upon. This, in turn, will improve the safety, compliance and efficacy of therapies and procedures ranging from the detection of infectious diseases, the treatment of autoimmune diseases, and the routine monitoring of health status.
描述(由申请人提供):目前检测诊断性蛋白质的方法需要耗费大量时间和资源的免疫化学技术,即使在理想情况下,也需要一个小时或更长时间才能将结果反馈给临床医生。这种缓慢的反应不符合现代医疗保健的时间框架,妨碍了患者的依从性,在某些情况下,还影响了药物和程序的有效性和安全性。(考虑一下:在不到15分钟内返回答案的诊断测试与需要30分钟的测试在质量上是不同的,因为后者需要与临床医生进行第二次互动。)在这里,我们提出了一种快速的,点护理的方法,同时检测多种诊断蛋白的发展。我们的方法,利用电化学来监测结合诱导的多肽或基于蛋白质的识别元件的折叠,将是快速的,特异性的,方便的,关键的,选择性的,足以直接应用于血清和-我们建议-全血。虽然我们最初的开发工作将集中在检测诊断HIV感染的蛋白质(如抗HIV抗体),但该方法将足以用于检测广泛的临床相关标记物。快速、可并行的即时诊断技术的发展可能会对从传染病检测、自身免疫性疾病治疗到健康状况常规监测等治疗和医疗程序的安全性、依从性和有效性产生重大影响。在这里,我们提出了一种无试剂的电化学平台,用于同时检测多种蛋白质的疾病诊断。所提议的技术将具有足够的快速、特异性和选择性,可以直接应用于护理点,从而显著提高分子诊断的速度,并根据其结果采取行动。反过来,这将提高从传染病检测、自身免疫性疾病治疗到健康状况常规监测等治疗和程序的安全性、依从性和有效性。

项目成果

期刊论文数量(22)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Beyond molecular beacons: optical sensors based on the binding-induced folding of proteins and polypeptides.
  • DOI:
    10.1002/chem.200701748
  • 发表时间:
    2009
  • 期刊:
  • 影响因子:
    4.3
  • 作者:
    Oh, Kenneth J.;Cash, Kevin J.;Plaxco, Kevin W.
  • 通讯作者:
    Plaxco, Kevin W.
Structure-switching biosensors: inspired by Nature.
结构开关生物传感器:受自然的启发。
A mechanistic study of electron transfer from the distal termini of electrode-bound, single-stranded DNAs.
The length and viscosity dependence of end-to-end collision rates in single-stranded DNA.
  • DOI:
    10.1016/j.bpj.2009.04.036
  • 发表时间:
    2009-07
  • 期刊:
  • 影响因子:
    3.4
  • 作者:
    T. Uzawa;R. R. Cheng-R.;K. Cash;D. Makarov;K. Plaxco
  • 通讯作者:
    T. Uzawa;R. R. Cheng-R.;K. Cash;D. Makarov;K. Plaxco
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Kevin W Plaxco其他文献

Kevin W Plaxco的其他文献

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{{ truncateString('Kevin W Plaxco', 18)}}的其他基金

Biostable nucleic acid aptamers for long-duration, in vivo molecular monitoring
用于长时间体内分子监测的生物稳定核酸适体
  • 批准号:
    10304801
  • 财政年份:
    2021
  • 资助金额:
    $ 22.71万
  • 项目类别:
Biostable nucleic acid aptamers for long-duration, in vivo molecular monitoring
用于长时间体内分子监测的生物稳定核酸适体
  • 批准号:
    10430240
  • 财政年份:
    2021
  • 资助金额:
    $ 22.71万
  • 项目类别:
Protein-folding-based in-vivo biosensors
基于蛋白质折叠的体内生物传感器
  • 批准号:
    10063408
  • 财政年份:
    2020
  • 资助金额:
    $ 22.71万
  • 项目类别:
Protein-folding-based in-vivo biosensors
基于蛋白质折叠的体内生物传感器
  • 批准号:
    10176410
  • 财政年份:
    2020
  • 资助金额:
    $ 22.71万
  • 项目类别:
Feedback controlled, ultra-high-precision drug delivery
反馈控制的超高精度药物输送
  • 批准号:
    10084266
  • 财政年份:
    2019
  • 资助金额:
    $ 22.71万
  • 项目类别:
Feedback controlled, ultra-high-precision drug delivery
反馈控制的超高精度药物输送
  • 批准号:
    10321612
  • 财政年份:
    2019
  • 资助金额:
    $ 22.71万
  • 项目类别:
Feedback controlled, ultra-high-precision drug delivery
反馈控制的超高精度药物输送
  • 批准号:
    9761770
  • 财政年份:
    2019
  • 资助金额:
    $ 22.71万
  • 项目类别:
Bio-electrochemical detectors for in vivo continuous monitoring
用于体内连续监测的生物电化学检测器
  • 批准号:
    9238429
  • 财政年份:
    2017
  • 资助金额:
    $ 22.71万
  • 项目类别:
Bio-electrochemical detectors for in vivo continuous monitoring
用于体内连续监测的生物电化学检测器
  • 批准号:
    9551624
  • 财政年份:
    2017
  • 资助金额:
    $ 22.71万
  • 项目类别:
A new approach to quantitative, point-of-care serology
定量、护理点血清学的新方法
  • 批准号:
    9306748
  • 财政年份:
    2014
  • 资助金额:
    $ 22.71万
  • 项目类别:

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神经性自身免疫性疾病中的自身抗体和抗体分泌细胞:从生物学到治疗
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母体免疫激活对后代自身免疫性疾病的影响
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IPP: AUTOIMMUNE DISEASES STATISTICAL AND CLINICAL COORDINATING CENTER (ADSCCC)
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针对半胱氨酸环受体的自身免疫性疾病的结构机制
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