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原位过滤辅助样品预处理与微波辅助蛋白质消化相结合的快速高效蛋白质组样品制备综合方法:imFASP

imFASP: An integrated approach combining in-situ filter-aided sample pretreatment with microwave-assisted protein digestion for fast and efficient proteome sample preparation.

作者信息

Zhao Qun, Fang Fei, Wu Ci, Wu Qi, Liang Yu, Liang Zhen, Zhang Lihua, Zhang Yukui

机构信息

Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Science, National Chromatographic Research and Analysis Center, 457 Zhongshan Road, Dalian, 116023, China.

Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Science, National Chromatographic Research and Analysis Center, 457 Zhongshan Road, Dalian, 116023, China; Graduate School of Chinese Academy of Sciences, Beijing, 100039, China.

出版信息

Anal Chim Acta. 2016 Mar 17;912:58-64. doi: 10.1016/j.aca.2016.01.049. Epub 2016 Feb 1.

Abstract

An integrated sample preparation method, termed "imFASP", which combined in-situ filter-aided sample pretreatment and microwave-assisted trypsin digestion, was developed for preparation of microgram and even nanogram amounts of complex protein samples with high efficiency in 1 h. For imFASP method, proteins dissolved in 8 M urea were loaded onto a filter device with molecular weight cut off (MWCO) as 10 kDa, followed by in-situ protein preconcentration, denaturation, reduction, alkylation, and microwave-assisted tryptic digestion. Compared with traditional in-solution sample preparation method, imFASP method generated more protein and peptide identifications (IDs) from preparation of 45 μg Escherichia coli protein sample due to the higher efficiency, and the sample preparation throughput was significantly improved by 14 times (1 h vs. 15 h). More importantly, when the starting amounts of E. coli cell lysate decreased to nanogram level (50-500 ng), the protein and peptide identified by imFASP method were improved at least 30% and 44%, compared with traditional in-solution preparation method, suggesting dramatically higher peptide recovery of imFASP method for trace amounts of complex proteome samples. All these results demonstrate that the imFASP method developed here is of high potential for high efficient and high throughput preparation of trace amounts of complex proteome samples.

摘要

一种名为“imFASP”的集成样品制备方法被开发出来,该方法结合了原位过滤辅助样品预处理和微波辅助胰蛋白酶消化,可在1小时内高效制备微克甚至纳克级的复杂蛋白质样品。对于imFASP方法,将溶解在8M尿素中的蛋白质加载到截留分子量(MWCO)为10kDa的过滤装置上,随后进行原位蛋白质预浓缩、变性、还原、烷基化和微波辅助胰蛋白酶消化。与传统的溶液内样品制备方法相比,由于效率更高,imFASP方法从45μg大肠杆菌蛋白质样品的制备中产生了更多的蛋白质和肽鉴定(ID),并且样品制备通量显著提高了14倍(1小时对15小时)。更重要的是,当大肠杆菌细胞裂解物的起始量降至纳克水平(50 - 500ng)时,与传统的溶液内制备方法相比,imFASP方法鉴定出的蛋白质和肽至少提高了30%和44%,这表明imFASP方法对于痕量复杂蛋白质组样品具有显著更高的肽回收率。所有这些结果表明,这里开发的imFASP方法在高效、高通量制备痕量复杂蛋白质组样品方面具有很高的潜力。

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