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使用含有单个保守氨基酸替换的标准肽评估蛋白质定量。

Evaluation of protein quantification using standard peptides containing single conservative amino acid replacements.

机构信息

Molecular Oncology and Proteomics, H. Lee Moffitt Cancer Center & Research Institute, University of South Florida, Tampa, FL 33612, USA.

出版信息

J Mass Spectrom. 2012 Feb;47(2):188-94. doi: 10.1002/jms.2053.

Abstract

Structural analogs are evaluated as peptide internal standards for protein quantification with liquid chromatography-multiple reaction monitoring mass spectrometry (LC-MRM); specifically, single conservative amino acid replacements (SCAR) are performed to create tagged standards that differ by the addition or subtraction of a single methylene group in one amino acid side chain. Because the performance of stable isotope-labeled standards (SIS) has been shown to be superior to structural analogs, differences in both development and quantitative performance between assays based on SIS and SCAR peptides are explored. To establish an assay using the structural analogs, analysis of endogenous, SCAR and SIS peptides was performed to examine their ion signal, fragmentation patterns and response in LC-MRM. Performance of SCAR and SIS peptides was compared for quantification of epidermal growth factor receptor from lung cancer cell lysates and immunoglobulin M in the serum of multiple myeloma patients.

摘要

结构类似物被评估为用于液相色谱-多重反应监测质谱法(LC-MRM)的蛋白质定量的肽内标;具体而言,通过单个保守氨基酸替换(SCAR)来创建标记标准,这些标记标准通过在一个氨基酸侧链中添加或减去单个亚甲基基团而有所不同。由于已经证明稳定同位素标记标准(SIS)的性能优于结构类似物,因此探索了基于 SIS 和 SCAR 肽的测定之间在开发和定量性能方面的差异。为了使用结构类似物建立测定方法,对内源性、SCAR 和 SIS 肽进行了分析,以检查它们在 LC-MRM 中的离子信号、碎裂模式和响应。比较了 SCAR 和 SIS 肽在定量肺癌细胞裂解物中的表皮生长因子受体和多发性骨髓瘤患者血清中的免疫球蛋白 M 方面的性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b49/3465614/5dbd1e4a8d5b/nihms403111f1.jpg

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