Advanced spectrometer with time-resolved mid-infrared and near-infrared capabilities for studies of membrane proteins and polymers
具有时间分辨中红外和近红外功能的先进光谱仪,用于膜蛋白和聚合物的研究
基本信息
- 批准号:RTI-2017-00032
- 负责人:
- 金额:$ 10.92万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Research Tools and Instruments
- 财政年份:2016
- 资助国家:加拿大
- 起止时间:2016-01-01 至 2017-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
FTIR spectroscopy is a powerful analytical technique, which enables researchers to look into structural properties of biological samples and polymers quickly and non-destructively. It can be used in static and time-resolved modes, where the latter allows following functional changes of biomolecules in real time. We request modern FTIR spectrometer with microsecond time-resolved capabilities (so called step-scan) and broad spectral range, which gives possibility to study not only proteins (mid-infrared) but also polymers and other complex media (near-infrared). We will apply these techniques to a wide range of scientific problems, ranging from studies of biologically and medically important membrane proteins serving as transporters of ions, water, and small molecules to structure of industrially relevant polymers. In particular, we will study novel microbial photosensors and light-driven ion pumps (microbial rhodopsins), human water channels (aquaporins) and hormone receptors (G-protein coupled receptors), and bacterial osmosensors (ProP). Besides serving as a powerful structural method by itself, FTIR will be also used as a quality control technique for another cutting-edge structural technique, solid-state NMR, for which University of Guelph has excellent facilities and active research program. Such research on structure and function of membrane proteins has broad biomedical impact, as these proteins constitute about a half of drug targets on the market. Finally, we will employ near-infrared capability of FTIR spectrometer to look at structural details of industrial polymers with the aim of rational design of their improved composition.
FTIR光谱是一种强大的分析技术,它使研究人员能够快速、非破坏性地研究生物样品和聚合物的结构特性。它可以在静态和时间分辨模式下使用,其中后者允许真实的时间内跟踪生物分子的功能变化。我们要求现代FTIR光谱仪具有微秒时间分辨能力(所谓的步进扫描)和宽光谱范围,这使得不仅可以研究蛋白质(中红外),还可以研究聚合物和其他复杂介质(近红外)。我们将把这些技术应用于广泛的科学问题,从研究作为离子、水和小分子转运蛋白的生物和医学重要膜蛋白到工业相关聚合物的结构。特别是,我们将研究新的微生物光传感器和光驱动离子泵(微生物视紫红质),人类水通道(水通道蛋白)和激素受体(G蛋白偶联受体),以及细菌的光传感器(ProP)。除了本身作为一种强大的结构方法外,FTIR还将被用作另一种尖端结构技术--固态NMR的质量控制技术,圭尔夫大学在这方面拥有出色的设施和积极的研究计划。这种对膜蛋白结构和功能的研究具有广泛的生物医学影响,因为这些蛋白质构成了市场上约一半的药物靶标。最后,我们将使用FTIR光谱仪的近红外功能来查看工业聚合物的结构细节,以合理设计其改进的组成。
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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Brown, Leonid其他文献
Mapping the Structure of an Integral Membrane Protein under Semi-Denaturing Conditions by Laser-Induced Oxidative Labeling and Mass Spectrometry
- DOI:
10.1016/j.jmb.2009.09.063 - 发表时间:
2009-12-18 - 期刊:
- 影响因子:5.6
- 作者:
Pan, Yan;Brown, Leonid;Konermann, Lars - 通讯作者:
Konermann, Lars
Site-Directed Mutagenesis Combined with Oxidative Methionine Labeling for Probing Structural Transitions of a Membrane Protein by Mass Spectrometry
- DOI:
10.1016/j.jasms.2010.08.004 - 发表时间:
2010-11-01 - 期刊:
- 影响因子:3.2
- 作者:
Pan, Yan;Brown, Leonid;Konermann, Lars - 通讯作者:
Konermann, Lars
Hydrogen/deuterium exchange mass spectrometry and optical spectroscopy as complementary tools for studying the structure and dynamics of a membrane protein
- DOI:
10.1016/j.ijms.2010.04.011 - 发表时间:
2011-04-30 - 期刊:
- 影响因子:1.8
- 作者:
Pan, Yan;Brown, Leonid;Konermann, Lars - 通讯作者:
Konermann, Lars
Kinetic Folding Mechanism of an Integral Membrane Protein Examined by Pulsed Oxidative Labeling and Mass Spectrometry
- DOI:
10.1016/j.jmb.2011.04.074 - 发表时间:
2011-07-01 - 期刊:
- 影响因子:5.6
- 作者:
Pan, Yan;Brown, Leonid;Konermann, Lars - 通讯作者:
Konermann, Lars
Brown, Leonid的其他文献
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{{ truncateString('Brown, Leonid', 18)}}的其他基金
New functionalities of microbial rhodopsins - where bioinformatics meets biophysics
微生物视紫红质的新功能——生物信息学与生物物理学的结合
- 批准号:
RGPIN-2018-04397 - 财政年份:2022
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
New functionalities of microbial rhodopsins - where bioinformatics meets biophysics
微生物视紫红质的新功能——生物信息学与生物物理学的结合
- 批准号:
RGPIN-2018-04397 - 财政年份:2021
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
New functionalities of microbial rhodopsins - where bioinformatics meets biophysics
微生物视紫红质的新功能——生物信息学与生物物理学的结合
- 批准号:
RGPIN-2018-04397 - 财政年份:2020
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
New functionalities of microbial rhodopsins - where bioinformatics meets biophysics
微生物视紫红质的新功能——生物信息学与生物物理学的结合
- 批准号:
RGPIN-2018-04397 - 财政年份:2019
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
New functionalities of microbial rhodopsins - where bioinformatics meets biophysics
微生物视紫红质的新功能——生物信息学与生物物理学的结合
- 批准号:
RGPIN-2018-04397 - 财政年份:2018
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
Mechanisms of triggering novel light-switchable functions in rhodopsins: enzymes and non-proton cation pumps
触发视紫红质新型光开关功能的机制:酶和非质子阳离子泵
- 批准号:
250202-2013 - 财政年份:2017
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
Mechanisms of triggering novel light-switchable functions in rhodopsins: enzymes and non-proton cation pumps
触发视紫红质新型光开关功能的机制:酶和非质子阳离子泵
- 批准号:
250202-2013 - 财政年份:2015
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
Mechanisms of triggering novel light-switchable functions in rhodopsins: enzymes and non-proton cation pumps
触发视紫红质新型光开关功能的机制:酶和非质子阳离子泵
- 批准号:
250202-2013 - 财政年份:2014
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
Mechanisms of triggering novel light-switchable functions in rhodopsins: enzymes and non-proton cation pumps
触发视紫红质新型光开关功能的机制:酶和非质子阳离子泵
- 批准号:
250202-2013 - 财政年份:2013
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
Retinal-binding proteins: new bioenergetic and photosensory mechanisms
视网膜结合蛋白:新的生物能和光传感机制
- 批准号:
250202-2007 - 财政年份:2012
- 资助金额:
$ 10.92万 - 项目类别:
Discovery Grants Program - Individual
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