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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >3-Mercaptopropionic acid modified ZnSe quantum dots as the matrix for direct surface-assisted laser desorption/ionization mass spectrometric analysis of peptides/proteins from sodium salt solution
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3-Mercaptopropionic acid modified ZnSe quantum dots as the matrix for direct surface-assisted laser desorption/ionization mass spectrometric analysis of peptides/proteins from sodium salt solution

机译:3-巯基丙酸修饰的ZnSe量子点作为基质,用于钠盐溶液中的肽/蛋白质的直接表面辅助激光解吸/电离质谱分析

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摘要

This study describes a strategy of using zinc selenium quantum dots (ZnSe QDs) modified with 3-mercaptopropionic acid (3-MPA) as the matrix for direct analysis of peptides and proteins from sodium salt solution in surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS). The enhancement of detection sensitivity for these biomolecules was due to the adsorption of positively charged peptides or proteins onto the surfaces of negatively charged ZnSe-3MPA QDs via electrostatic interactions resulting in an increase in ionization efficiency for sodium adduct ions ([M+Na]+). The applicability of the current approach was demonstrated for a variety of peptides, including leucine-enkephalin, methione-enkephalin, HW6, substance P and angiotensin II, and proteins (cytochrome c, myoglobin and lysozyme). Signal intensities of these peptides or proteins can be enhanced by 25-95 times compared with those obtained by LDI-MS in the absence of ZnSe-3MPA QDs. Applying ZnSe-3MPA QDs to serve as the matrix in SALDI-MS is a simple and effective approach for direct analysis of peptide and protein molecules from sodium salt solution without any pretreatment as the peptides and proteins can be successfully detected as sodium adduct ions ([M+Na]~+).
机译:本研究描述了一种使用3-巯基丙酸(3-MPA)修饰的锌硒量子点(ZnSe QDs)作为基质在表面辅助激光解吸/电离质谱中直接分析钠盐溶液中的肽和蛋白质的策略(SALDI-MS)。这些生物分子检测灵敏度的提高是由于带正电的肽或蛋白质通过静电相互作用吸附到带负电的ZnSe-3MPA QD表面上,从而导致钠加合离子([M + Na] + )。证明了当前方法对多种肽的适用性,包括亮氨酸-脑啡肽,甲硫氨酸-脑啡肽,HW6,P物质和血管紧张素II,以及蛋白质(细胞色素c,肌红蛋白和溶菌酶)。与没有ZnSe-3MPA QD的LDI-MS相比,这些肽或蛋白质的信号强度可以提高25-95倍。将ZnSe-3MPA QD用作SALDI-MS中的基质是一种简单有效的方法,无需进行任何预处理即可直接从钠盐溶液直接分析肽和蛋白质分子,因为肽和蛋白质可以成功检测为钠加合物离子([ M + Na]〜+)。

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