Whiteaker Jeffrey R, Zhao Lei, Schoenherr Regine M, Kennedy Jacob J, Ivey Richard G, Paulovich Amanda G
Fred Hutchinson Cancer Research Center, 1100 Fairview Ave. N. E2-112, Seattle, WA, 98109, USA.
Methods Mol Biol. 2017;1599:197-213. doi: 10.1007/978-1-4939-6955-5_15.
Peptide immunoaffinity enrichment coupled with targeted mass spectrometry is a quantitative approach for the robust and reproducible quantification of peptide analytes. The approach is capable of multiplexed quantification of peptides, including posttranslational modifications such as phosphorylation. Anti-peptide antibodies are used to enrich analytes and heavy stable isotope-labeled standards. The enriched peptides are directly measured by multiple reaction monitoring (MRM), a well-characterized quantitative mass spectrometry-based method. Quantification is performed by measuring the analyte (light) peptide response relative to the heavy standard, which is spiked at a known concentration. Here, we describe the methodology for multiplexed measurement of phosphorylated peptides on the ATM kinase and their nonmodified peptide analogs in cellular lysates. The method provides quantitative measurements of phospho-signaling and can be extended to a number of other phosphopeptides and sample types.
肽免疫亲和富集结合靶向质谱分析是一种用于对肽分析物进行可靠且可重复定量的定量方法。该方法能够对肽进行多重定量,包括翻译后修饰如磷酸化。抗肽抗体用于富集分析物和重稳定同位素标记的标准品。富集的肽通过多反应监测(MRM)直接测量,MRM是一种特征明确的基于定量质谱的方法。通过测量分析物(轻)肽相对于以已知浓度加入的重标准品的响应来进行定量。在此,我们描述了在细胞裂解物中对ATM激酶上的磷酸化肽及其未修饰的肽类似物进行多重测量的方法。该方法提供了磷酸化信号的定量测量,并且可以扩展到许多其他磷酸肽和样品类型。