Wellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, UK.
Chair of Bioanalytics, Technische Universität Berlin, Berlin, Germany.
Proteomics. 2024 Sep;24(17):e2300385. doi: 10.1002/pmic.202300385. Epub 2024 Jul 12.
The mzIdentML data format, originally developed by the Proteomics Standards Initiative in 2011, is the open XML data standard for peptide and protein identification results coming from mass spectrometry. We present mzIdentML version 1.3.0, which introduces new functionality and support for additional use cases. First of all, a new mechanism for encoding identifications based on multiple spectra has been introduced. Furthermore, the main mzIdentML specification document can now be supplemented by extension documents which provide further guidance for encoding specific use cases for different proteomics subfields. One extension document has been added, covering additional use cases for the encoding of crosslinked peptide identifications. The ability to add extension documents facilitates keeping the mzIdentML standard up to date with advances in the proteomics field, without having to change the main specification document. The crosslinking extension document provides further explanation of the crosslinking use cases already supported in mzIdentML version 1.2.0, and provides support for encoding additional scenarios that are critical to reflect developments in the crosslinking field and facilitate its integration in structural biology. These are: (i) support for cleavable crosslinkers, (ii) support for internally linked peptides, (iii) support for noncovalently associated peptides, and (iv) improved support for encoding scores and the corresponding thresholds.
mzIdentML 数据格式最初由蛋白质组学标准倡议于 2011 年开发,是用于从质谱获得的肽和蛋白质鉴定结果的开放 XML 数据标准。我们现在介绍 mzIdentML 版本 1.3.0,它引入了新功能并支持更多用例。首先,引入了一种基于多个光谱进行鉴定编码的新机制。此外,现在可以在主要的 mzIdentML 规范文档中添加扩展文档,为不同蛋白质组学子领域的特定用例的编码提供进一步的指导。添加了一个扩展文档,涵盖了用于交叉连接肽鉴定编码的其他用例。添加扩展文档的功能有助于使 mzIdentML 标准与蛋白质组学领域的进展保持同步,而无需更改主要规范文档。交联扩展文档提供了对 mzIdentML 版本 1.2.0 中已经支持的交联用例的进一步解释,并为编码反映交联领域发展和促进其在结构生物学中的整合的关键场景提供了支持。这些是:(i)支持可裂解交联剂,(ii)支持内部连接的肽,(iii)支持非共价结合的肽,以及(iv)改进了对编码分数和相应阈值的支持。