Department of Microbiology and Immunology, Dalhousie University, Halifax, B3H 4R2, Canada.
Department of Pathology, Dalhousie University, Halifax, B3H 4R2, Canada.
Proteomics. 2019 Mar;19(5):e1800458. doi: 10.1002/pmic.201800458. Epub 2019 Feb 19.
MHC class I (MHC-I)-bound ligands play a pivotal role in CD8 T cell immunity and are hence of major interest in understanding and designing immunotherapies. One of the most commonly utilized approaches for detecting MHC ligands is LC-MS/MS. Unfortunately, the effectiveness of current algorithms to identify MHC ligands from LC-MS/MS data is limited because the search algorithms used were originally developed for proteomics approaches detecting tryptic peptides. Consequently, the analysis often results in inflated false discovery rate (FDR) statistics and an overall decrease in the number of peptides that pass FDR filters. Andreatta et al. describe a new scoring tool (MS-rescue) for peptides from MHC-I immunopeptidome datasets. MS-rescue incorporates the existence of MHC-I peptide motifs to rescore peptides from ligandome data. The tool is demonstrated here using peptides assigned from LC-MS/MS data with PEAKs software but can be deployed on data from any search algorithm. This new approach increased the number of peptides identified by up to 20-30% and promises to aid the discovery of novel MHC-I ligands with immunotherapeutic potential.
MHC I 类(MHC-I)结合配体在 CD8 T 细胞免疫中起着关键作用,因此在理解和设计免疫疗法方面具有重要意义。检测 MHC 配体最常用的方法之一是 LC-MS/MS。不幸的是,当前用于从 LC-MS/MS 数据中识别 MHC 配体的算法的有效性有限,因为用于检测胰蛋白酶肽的原始搜索算法最初是为蛋白质组学方法开发的。因此,分析通常会导致虚报率(FDR)统计数据膨胀,并且通过 FDR 过滤器的肽的总数总体减少。Andreatta 等人描述了一种用于 MHC-I 免疫肽组数据集的肽的新评分工具(MS-rescue)。MS-rescue 将 MHC-I 肽基序的存在纳入配体组数据的肽重新评分中。该工具在此处使用 PEAKs 软件分配的 LC-MS/MS 数据中的肽进行了演示,但可以部署在任何搜索算法的数据上。这种新方法将鉴定的肽的数量增加了 20-30%,有望有助于发现具有免疫治疗潜力的新型 MHC-I 配体。