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MSRescore:数据驱动的重新评分极大地提高了免疫肽识别率。

MSRescore: Data-Driven Rescoring Dramatically Boosts Immunopeptide Identification Rates.

机构信息

VIB-UGent Center for Medical Biotechnology, VIB, Zwijnaarde, Belgium; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.

Laboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Université de Strasbourg, CNRS, Strasbourg, France.

出版信息

Mol Cell Proteomics. 2022 Aug;21(8):100266. doi: 10.1016/j.mcpro.2022.100266. Epub 2022 Jul 6.

DOI:10.1016/j.mcpro.2022.100266
PMID:35803561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9411678/
Abstract

Immunopeptidomics aims to identify major histocompatibility complex (MHC)-presented peptides on almost all cells that can be used in anti-cancer vaccine development. However, existing immunopeptidomics data analysis pipelines suffer from the nontryptic nature of immunopeptides, complicating their identification. Previously, peak intensity predictions by MSPIP and retention time predictions by DeepLC have been shown to improve tryptic peptide identifications when rescoring peptide-spectrum matches with Percolator. However, as MSPIP was tailored toward tryptic peptides, we have here retrained MSPIP to include nontryptic peptides. Interestingly, the new models not only greatly improve predictions for immunopeptides but also yield further improvements for tryptic peptides. We show that the integration of new MSPIP models, DeepLC, and Percolator in one software package, MSRescore, increases spectrum identification rate and unique identified peptides with 46% and 36% compared to standard Percolator rescoring at 1% FDR. Moreover, MSRescore also outperforms the current state-of-the-art in immunopeptide-specific identification approaches. Altogether, MSRescore thus allows substantially improved identification of novel epitopes from existing immunopeptidomics workflows.

摘要

免疫肽组学旨在鉴定几乎所有细胞表面呈现的主要组织相容性复合体 (MHC) 肽,这些肽可用于开发抗癌疫苗。然而,现有的免疫肽组学数据分析流程受到免疫肽的非酶切性质的影响,这使得它们的鉴定变得复杂。此前,MSPIP 的峰强度预测和 DeepLC 的保留时间预测已被证明可通过 Percolator 对肽谱匹配进行重新评分时,提高酶切肽的鉴定率。然而,由于 MSPIP 是专门针对酶切肽设计的,因此我们在这里重新训练了 MSPIP 以包括非酶切肽。有趣的是,新模型不仅大大提高了免疫肽的预测能力,而且对酶切肽也有进一步的提高。我们表明,将新的 MSPIP 模型、DeepLC 和 Percolator 集成到一个软件包 MSRescore 中,与标准的 Percolator 重新评分相比,可将谱识别率提高 46%,将独特鉴定的肽提高 36%,在 FDR 为 1%的情况下。此外,MSRescore 还优于目前针对免疫肽的特定识别方法的最新水平。总的来说,MSRescore 因此允许从现有的免疫肽组学工作流程中大大提高新表位的鉴定能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/88962a8e91ef/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/4c0e47df40b4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/39938f4ba21e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/c18085b2e9e8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/88962a8e91ef/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/4c0e47df40b4/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/39938f4ba21e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/c18085b2e9e8/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60ec/9411678/88962a8e91ef/gr3.jpg

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