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通过微流控电捕获进行肽富集以用于电喷雾质谱在线分析。

Peptide enrichment by microfluidic electrocapture for online analysis by electrospray mass spectrometry.

作者信息

Vollmer Susanne, Astorga-Wells Juan, Alvelius Gunvor, Bergman Tomas, Jörnvall Hans

机构信息

Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 77 Stockholm, Sweden.

出版信息

Anal Biochem. 2008 Mar 1;374(1):154-62. doi: 10.1016/j.ab.2007.09.017. Epub 2007 Sep 20.

Abstract

Identification of peptides from a complex mixture can be difficult because of the wide concentration range and the different ionization efficiencies of peptides during analysis by electrospray ionization (ESI) mass spectrometry (MS). Preconcentration methods are necessary to allow low-abundance and low-intensity peptides to reach the ionization threshold of the mass spectrometer. Here we demonstrate peptide enrichment based on electroimmobilization. Peptides are immobilized without the use of solid support or chemical binding by application of an electric field along a microflow stream in an electrocapture cell. Once enriched/preconcentrated inside the cell, they are released by removal of the electric field and via an interface with an electrospray emitter are submitted to online mass spectrometric analysis. Tandem mass spectrometric analysis of a peptide mixture containing hemoglobin, myoglobin, bovine serum albumin (BSA), and cytochrome c was successful. Amplification factors up to 16-fold were achieved with improvement of the signal-to-noise values for the preconcentrated sample. The limit of detection for one of the preconcentrated peptides was 3.6 fmol.

摘要

由于复杂混合物中肽段的浓度范围广泛,且在电喷雾电离(ESI)质谱分析(MS)过程中肽段的电离效率不同,从复杂混合物中鉴定肽段可能会很困难。预浓缩方法对于使低丰度和低强度的肽段达到质谱仪的电离阈值是必要的。在此,我们展示了基于电固定的肽段富集方法。通过在电捕获池中沿微流通道施加电场,肽段无需使用固体支持物或化学结合即可被固定。一旦在池中富集/预浓缩,通过去除电场将其释放,并通过与电喷雾发射器的接口进行在线质谱分析。对含有血红蛋白、肌红蛋白、牛血清白蛋白(BSA)和细胞色素c的肽段混合物进行串联质谱分析获得成功。预浓缩样品的信噪比得到改善,实现了高达16倍的放大因子。其中一种预浓缩肽段的检测限为3.6飞摩尔。

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