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结合毛细管电泳基质辅助激光解吸/电离质谱和稳定同位素标记技术进行甲壳动物比较肽组学研究。

Combining capillary electrophoresis matrix-assisted laser desorption/ionization mass spectrometry and stable isotopic labeling techniques for comparative crustacean peptidomics.

机构信息

School of Pharmacy and Department of Chemistry, University of Wisconsin-Madison, Madison, WI 53705-2222, USA.

出版信息

J Chromatogr A. 2010 Jun 25;1217(26):4463-70. doi: 10.1016/j.chroma.2010.02.084. Epub 2010 Mar 6.

Abstract

Herein we describe a sensitive and straightforward off-line capillary electrophoresis (CE) matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) interface in conjunction with stable isotopic labeling (SIL) technique for comparative neuropeptidomic analysis in crustacean model organisms. Two SIL schemes, including a binary H/D formaldehyde labeling technique and novel, laboratory-developed multiplexed dimethylated leucine-based isobaric tagging reagents, have been evaluated in these proof-of-concept experiments. We employ these isotopic labeling techniques in conjunction with CE-MALDI-MS for quantitative peptidomic analyses of the pericardial organs isolated from two crustacean species, the European green crab Carcinus maenas and the blue crab Callinectes sapidus. Isotopically labeled peptide pairs are found to co-migrate in CE fractions and quantitative changes in relative abundances of peptide pairs are obtained by comparing peak intensities of respective peptide pairs. Several neuropeptide families exhibit changes in response to salinity stress, suggesting potential physiological functions of these signaling peptides.

摘要

在这里,我们描述了一种灵敏且直接的离线毛细管电泳(CE)-基质辅助激光解吸/电离质谱(MALDI-MS)接口,结合稳定同位素标记(SIL)技术,用于甲壳动物模型生物中的比较神经肽组学分析。在这些概念验证实验中,我们评估了两种 SIL 方案,包括二元 H/D 甲醛标记技术和新开发的实验室多路复用二甲基化亮氨酸等排标记试剂。我们将这些同位素标记技术与 CE-MALDI-MS 结合,用于从两种甲壳类动物,欧洲绿蟹(Carcinus maenas)和蓝蟹(Callinectes sapidus)的围心器官中进行定量肽组学分析。发现同位素标记的肽对在 CE 馏分中共同迁移,并通过比较各自肽对的峰强度来获得肽对相对丰度的定量变化。几种神经肽家族对盐度胁迫表现出变化,这表明这些信号肽具有潜在的生理功能。

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