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通过尺寸排阻色谱预分级和纳升液相色谱-串联质谱鉴定对小鼠肝脏进行全面的肽组分析。

Comprehensive peptidome analysis of mouse livers by size exclusion chromatography prefractionation and nanoLC-MS/MS identification.

作者信息

Hu Lianghai, Li Xin, Jiang Xinning, Zhou Houjiang, Jiang Xiaogang, Kong Liang, Ye Mingliang, Zou Hanfa

机构信息

National Chromatographic R&A Center, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China.

出版信息

J Proteome Res. 2007 Feb;6(2):801-8. doi: 10.1021/pr060469e.

Abstract

Peptidome analysis has received increasing attention in recent years. Cancer diagnosis by serum peptidome has also been reported by peptides' profiling for discovery of peptide biomarkers. Tissue, which may have a higher biomarker concentration than blood, has not been investigated extensively by means of peptidome analysis. Here, a method for the peptidome analysis of mouse liver was developed by the combination of size exclusion chromatography (SEC) prefractionation with nano-liquid chromatography-tamdem mass spectrometry (nanoLC-MS/MS) analysis. The extracted peptides from mouse liver were separated according to their molecular weight using a size exclusion column. MALDI-TOF MS was used to characterize the molecular weight distribution of the peptides in fractions eluted from the SEC column. The low molecular weight (LMW) (MW < 3000 Da) peptides in the collected fractions were directly analyzed by LC-MS/MS which resulted in the identification of 1181 unique peptides (from 371 proteins). The high molecular weight (HMW) (MW > 3000 Da) peptides in the early two fractions from the SEC column were first digested with trypsin, and the resulted digests were then analyzed by LC-MS/MS, which led to the identification of 123 and 127 progenitor proteins of the HMW peptides in fractions 1 and 2, respectively. Analysis of the peptides' cleavage sites showed that the peptides are cleaved in regulation, which may reflect the protease activity and distribution in body, and also represent the biological state of the tissue and provide a fresh source for biomarker discovery.

摘要

近年来,肽组分析受到了越来越多的关注。通过肽谱分析发现肽生物标志物,血清肽组用于癌症诊断的研究也已有报道。组织中的生物标志物浓度可能高于血液,但尚未通过肽组分析进行广泛研究。在此,通过尺寸排阻色谱(SEC)预分级与纳升液相色谱-串联质谱(nanoLC-MS/MS)分析相结合的方法,开发了一种用于小鼠肝脏肽组分析的方法。从小鼠肝脏中提取的肽使用尺寸排阻柱根据其分子量进行分离。基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)用于表征从SEC柱洗脱的级分中肽的分子量分布。收集的级分中的低分子量(LMW)(MW < 3000 Da)肽直接通过LC-MS/MS进行分析,结果鉴定出1181种独特的肽(来自371种蛋白质)。SEC柱前两个级分中的高分子量(HMW)(MW > 3000 Da)肽首先用胰蛋白酶消化,然后对所得消化产物进行LC-MS/MS分析,结果分别在第1和第2级分中鉴定出123种和127种HMW肽的前体蛋白。对肽切割位点的分析表明,肽的切割具有规律性,这可能反映了蛋白酶在体内的活性和分布,也代表了组织的生物学状态,并为生物标志物的发现提供了新的来源。

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