A Novel Mass Spectrometric Ion Source for Proteomics

用于蛋白质组学的新型质谱离子源

• 批准号: 6823270
• 负责人: JOSHUA J COON
• 金额: $ 3.99万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-09-01 至 2005-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6823270
• 关键词: acute myelogenous leukemia; biomarker; biotechnology; chromatography; high performance liquid chromatography; ionization; mass spectrometry; matrix assisted laser desorption ionization; method development; postdoctoral investigator; protein sequence; proteomics

DESCRIPTION (provided by applicant): The overall goals of this research are: (1) to develop a novel high performance liquid chromatography electrospray/ matrix-assisted laser desorption/ionization-mass spectrometry (HPLC-ESI/MALDI-MS) interface to enhance the mass spectrometric identification and sequence analysis of proteins in complex mixtures and (2) to employ this technology to solve problems at the forefront of biological research. The specific aims are to: (1) develop a novel ionization method for mass spectrometry that is capable of increasing proteome coverage, while at the same time providing a more rapid and inexpensive approach for the analysis of proteins in complex mixtures and (2) to apply developed technology to identify proteins that function as diagnostic markers or potential drug targets for acute myeloid leukemias. By operating at atmospheric pressure, the technique will eliminate many of the barriers encountered when combining MALDI with microcapillary HPLC. The method will utilize ESI aerosol droplets to serve as a platform for MALDI ion generation. And unlike any other HPLC-MS approach, this method will capitalize the favorable attributes of both ionization methods simultaneously. This technology will be applied to determine the regulatory pathways involved with the mixed lineage leukemia gene (MLL), which is a common target for chromosome translocation that often results in acute myeloid leukemias. Utilizing HPLC-ESI/MALDI-MS, we propose to identify proteins, induced by the MLL-ENL fusion protein that could function as biomarkers or potential drug targets for treatment of acute myeloid leukemias.

描述（由申请人提供）：本研究的总体目标是：（1）开发一种新型高效液相色谱电喷雾/基质辅助激光解吸/电离质谱（HPLC-ESI/MALDI-MS）接口，以增强复杂混合物中蛋白质的质谱鉴定和序列分析，以及（2）采用该技术解决生物学研究前沿的问题。具体目标是：（1）开发一种新的质谱电离方法，能够增加蛋白质组覆盖率，同时提供一种更快速、更廉价的方法来分析复杂混合物中的蛋白质;（2）应用已开发的技术来鉴定作为急性髓性白血病诊断标志物或潜在药物靶点的蛋白质。通过在大气压下操作，该技术将消除MALDI与微毛细管HPLC相结合时遇到的许多障碍。该方法将利用ESI气溶胶液滴作为MALDI离子产生的平台。与任何其他HPLC-MS方法不同，该方法将同时利用两种电离方法的有利属性。这项技术将被应用于确定与混合谱系白血病基因（MLL），这是一个常见的目标染色体易位，往往导致急性髓性白血病涉及的调控途径。利用HPLC-ESI/MALDI-MS，我们建议鉴定MLL-ENL融合蛋白诱导的蛋白质，这些蛋白质可以作为治疗急性髓性白血病的生物标志物或潜在的药物靶点。