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用于基质辅助激光解吸电离质谱分析受保护合成肽的优化样品制备方法。

Optimized sample preparation for MALDI mass spectrometry analysis of protected synthetic peptides.

作者信息

Schaiberger Audrey M, Moss Jason A

机构信息

Roche Colorado Corporation, Boulder Technology Center, Boulder, CO 80301, USA.

出版信息

J Am Soc Mass Spectrom. 2008 Apr;19(4):614-9. doi: 10.1016/j.jasms.2008.01.010. Epub 2008 Jan 31.

DOI:10.1016/j.jasms.2008.01.010
PMID:18295503
Abstract

The recent development and commercialization of Fuzeon (enfuvirtide) demonstrated that a convergent strategy comprised of both solid- and solution-phase synthetic methodologies presents a viable route for peptide manufacturing on a multi-ton scale. In this strategy, the target sequence is prepared by stepwise solid-phase synthesis of protected peptide fragments, which are then coupled together in the solution-phase to give the full-length sequence. These synthetic methodologies pose a unique challenge for mass spectrometry (MS), as protected peptide intermediates are often marked by poor solubility, structural lability, and low ionization potential. Matrix-assisted laser desorption/ionization (MALDI) MS is uniquely suited to such analytes; however, generalized protocols for MALDI analysis of protected peptides have yet to be demonstrated. Herein, we report an operationally simple sample preparation method for MALDI analysis of protected peptides, which greatly facilitates the collection and interpretation of MS data. In this method, the difficulty in MS analysis of protected peptides has been greatly diminished by use of dithranol as a matrix and CsCl as an additive, giving rise to intentionally-formed Cs(+) adducts. With greatly reduced fragmentation, better crystalline morphology, and easier data interpretation, we anticipate that these findings will find utility in peptide process development and manufacturing settings for reaction monitoring, troubleshooting, and quality control.

摘要

福泽昂(恩夫韦肽)最近的研发和商业化表明,由固相和溶液相合成方法组成的汇聚策略为多吨规模的肽生产提供了一条可行途径。在该策略中,目标序列通过受保护肽片段的逐步固相合成来制备,然后在溶液相中偶联在一起以得到全长序列。这些合成方法对质谱分析(MS)提出了独特挑战,因为受保护的肽中间体通常具有溶解性差、结构不稳定和电离电位低的特点。基质辅助激光解吸/电离(MALDI)质谱特别适合此类分析物;然而,用于受保护肽的MALDI分析的通用方案尚未得到验证。在此,我们报告了一种操作简单的用于受保护肽的MALDI分析的样品制备方法,该方法极大地促进了质谱数据的收集和解读。在该方法中,通过使用连二亚硫酸钠作为基质和CsCl作为添加剂,受保护肽的质谱分析难度大大降低,产生了有意形成的Cs(+)加合物。由于碎片大大减少、晶体形态更好且数据解读更容易,我们预计这些发现将在肽工艺开发和生产环境中用于反应监测、故障排除和质量控制。

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