GAS PHASE ION SEPARATIONS FOR COMB LIBRARY ANALYSIS
用于梳库分析的气相离子分离
基本信息
- 批准号:6490187
- 负责人:
- 金额:$ 14.31万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2000
- 资助国家:美国
- 起止时间:2000-01-01 至 2003-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
This proposal describes a program for developing gas-phase ion separation strategies for the analysis of complex biomolecular mixtures such as combinatorial libraries. Preliminary data show that a new ion mobility/time-of-flight mass spectrometry technique combined with electrospray ionization allows components of complex peptide mixtures to be simultaneously characterized. Th this approach the components of the mixture are ionized and the ions are separated by differences in their mobilities through an inert buffer gas before being dispersed into a mass spectrometer. The gas-phase separation step allows structural and sequence isomers to be distinguished. An important feature of the proposal is the development of instrumentation that is capable of parallel sequencing of multiple mobility-separated components of a mixture. This is feasible because fragment ions will be formed after mobility separation and thus are labeled according to parent ion mobilities. Applications of the proposed techniques to several types of libraries (peptide, oligonucleotide, and organic molecule) are outlined. The ability to characterize isomers within a given m/z ratio will have a tremendous impact on the utility of mass spectrometric methods in revealing whether or not expected library components are truly present. This will be a powerful tool in refinement of synthetic methods, and will provide opportunities for development of new search strategies.
本提案描述了一个开发气相离子分离策略的程序,用于分析复杂的生物分子混合物,如组合文库。初步数据表明,一种新的离子迁移率/飞行时间质谱技术结合电喷雾电离可以同时表征复杂肽混合物的成分。在这种方法中,混合物的成分被电离,离子通过惰性缓冲气体通过其迁移率的差异被分离,然后被分散到质谱仪中。气相分离步骤允许区分结构和序列异构体。该提案的一个重要特征是开发能够对混合物的多个流动性分离组分进行平行测序的仪器。这是可行的,因为碎片离子会在迁移率分离后形成,从而根据母离子迁移率进行标记。提出的技术应用于几种类型的文库(肽,寡核苷酸和有机分子)概述。在给定的m/z比内表征同分异构体的能力将对质谱方法的效用产生巨大影响,以揭示期望的库成分是否真正存在。这将是改进合成方法的有力工具,并将为开发新的搜索策略提供机会。
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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DAVID E. CLEMMER其他文献
DAVID E. CLEMMER的其他文献
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{{ truncateString('DAVID E. CLEMMER', 18)}}的其他基金
Administrative Supplement to Characterizing proteasome-substrate interactions by mass spectrometry proteomics
通过质谱蛋白质组学表征蛋白酶体-底物相互作用的行政补充
- 批准号:
10388694 - 财政年份:2020
- 资助金额:
$ 14.31万 - 项目类别:
Characterizing proteasome-substrate interactions by mass spectrometry proteomics
通过质谱蛋白质组学表征蛋白酶体-底物相互作用
- 批准号:
10200097 - 财政年份:2020
- 资助金额:
$ 14.31万 - 项目类别:
Characterizing proteasome-substrate interactions by mass spectrometry proteomics
通过质谱蛋白质组学表征蛋白酶体-底物相互作用
- 批准号:
10377447 - 财政年份:2020
- 资助金额:
$ 14.31万 - 项目类别:
Developing High-Resolution Ion Mobility Spectrometry-Charge Detection-Mass Spectrometry for Rapid Analysis in the Megadalton to Gigadalton Regime
开发高分辨率离子淌度谱-电荷检测-质谱法,以实现兆道尔顿到千兆道尔顿范围内的快速分析
- 批准号:
10061629 - 财政年份:2018
- 资助金额:
$ 14.31万 - 项目类别:
Developing High-Resolution Ion Mobility Spectrometry-Charge Detection-Mass Spectrometry for Rapid Analysis in the Megadalton to Gigadalton Regime
开发高分辨率离子淌度谱-电荷检测-质谱法,以实现兆道尔顿到千兆道尔顿范围内的快速分析
- 批准号:
10295181 - 财政年份:2018
- 资助金额:
$ 14.31万 - 项目类别:
Development of high resolution mobility measurements for structural biology
结构生物学高分辨率迁移率测量的开发
- 批准号:
9383630 - 财政年份:2017
- 资助金额:
$ 14.31万 - 项目类别:
New proteome techniques: mapping adult D. Melanogaster
新的蛋白质组技术:绘制成年黑腹果蝇图谱
- 批准号:
9146961 - 财政年份:2015
- 资助金额:
$ 14.31万 - 项目类别:
New proteome techniques: mapping adult D. Melanogaster
新蛋白质组技术:绘制成年黑腹果蝇图谱
- 批准号:
9009178 - 财政年份:2015
- 资助金额:
$ 14.31万 - 项目类别:
2011 Biological Molecules in the Gas Phase and in Solution GRC
2011 气相和溶液中的生物分子 GRC
- 批准号:
8193187 - 财政年份:2011
- 资助金额:
$ 14.31万 - 项目类别:
Developing high-throughput IMS-MS and IMS-IMS-MS techniques for glycomics analysi
开发用于糖组学分析的高通量 IMS-MS 和 IMS-IMS-MS 技术
- 批准号:
7887486 - 财政年份:2010
- 资助金额:
$ 14.31万 - 项目类别: