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利用基质辅助激光解吸电离源内衰变质谱分析进行聚乙二醇化位点的自上而下测定

Toward top-down determination of PEGylation site using MALDI in-source decay MS analysis.

作者信息

Yoo Chul, Suckau Detlev, Sauerland Volker, Ronk Michael, Ma Minhui

机构信息

Analytical Research and Development, Amgen Inc., Thousand Oaks, California 91320, USA.

出版信息

J Am Soc Mass Spectrom. 2009 Feb;20(2):326-33. doi: 10.1016/j.jasms.2008.10.013. Epub 2008 Nov 1.

Abstract

A novel matrix assisted laser desorption/ionization (MALDI)-based mass spectrometric approach has been evaluated to rapidly analyze a custom designed PEGylated peptide that is 31 residues long and conjugated with 20 kDa linear polyethylene glycol (PEG) at the side chain of Lys. MALDI-TOF MS provided sufficiently high resolution to allow observation of each of the oligomers of the heterogeneous PEGylated peptide (m/Deltam of ca. 500), while a typical ESI-MS spectrum of this molecule was extremely complex and unresolved. Reflector in-source decay (reISD) analysis using MALDI-TOF MS was attempted to identify the PEGylation site at intact molecular level without any sample treatment. An reISD spectrum of the free peptide was observed with abundant c-, y-, and [z + 2]-fragment ion series, whereas, in the fragmented PEGylated peptide, the fragment ion series were truncated at the residue where PEG was attached. Therefore, a direct comparison of these top-down reISD spectra suggested the location of the PEGylation site. Results from this study demonstrate a clear analytical utility of the ISD technique to characterize structural aspects of heterogeneous biomolecules.

摘要

一种基于新型基质辅助激光解吸/电离(MALDI)的质谱方法已被评估,用于快速分析一种定制设计的聚乙二醇化肽,该肽长31个残基,在赖氨酸侧链与20 kDa线性聚乙二醇(PEG)共轭。MALDI-TOF MS提供了足够高的分辨率,能够观察到异质聚乙二醇化肽的每种寡聚体(约500的m/Δm),而该分子的典型ESI-MS谱极其复杂且无法解析。尝试使用MALDI-TOF MS进行反射器源内衰变(reISD)分析,以在不进行任何样品处理的情况下在完整分子水平鉴定聚乙二醇化位点。观察到游离肽的reISD谱具有丰富的c-、y-和[z + 2]-片段离子系列,而在片段化的聚乙二醇化肽中,片段离子系列在PEG连接的残基处被截断。因此,这些自上而下的reISD谱的直接比较表明了聚乙二醇化位点的位置。本研究结果证明了ISD技术在表征异质生物分子结构方面的明显分析效用。

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