Automated annotation and visualisation of high-resolution spatial proteomic mass spectrometry imaging data using HIT-MAP

被引:44
|
作者
Guo, G. [1 ,2 ]
Papanicolaou, M. [3 ,4 ,5 ]
Demarais, N. J. [1 ,2 ]
Wang, Z. [6 ]
Schey, K. L. [6 ]
Timpson, P. [3 ,4 ,7 ]
Cox, T. R. [3 ,4 ,7 ]
Grey, A. C. [1 ,2 ]
机构
[1] Univ Auckland, Mass Spectrometry Hub, Auckland, New Zealand
[2] Univ Auckland, Sch Biol Sci, Auckland, New Zealand
[3] UNSW Sydney, Garvan Inst Med Res, Sydney, NSW, Australia
[4] UNSW Sydney, Kinghorn Canc Ctr, Sydney, NSW, Australia
[5] Univ Technol Sydney, Sch Life Sci, Sydney, NSW, Australia
[6] Vanderbilt Univ, Dept Biochem, Nashville, TN 37232 USA
[7] UNSW Sydney, Fac Med, St Vincents Clin Sch, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
INTEGRAL MEMBRANE-PROTEINS; RAT-BRAIN; MALDI-TOF; CYTOCHROME-OXIDASE; TISSUE; IDENTIFICATION; PEPTIDES; LENS; MS; PURIFICATION;
D O I
10.1038/s41467-021-23461-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Spatial proteomics has the potential to significantly advance our understanding of biology, physiology and medicine. Matrix-assisted laser desorption/ionisation mass spectrometry imaging (MALDI-MSI) is a powerful tool in the spatial proteomics field, enabling direct detection and registration of protein abundance and distribution across tissues. MALDI-MSI preserves spatial distribution and histology allowing unbiased analysis of complex, heterogeneous tissues. However, MALDI-MSI faces the challenge of simultaneous peptide quantification and identification. To overcome this, we develop and validate HIT-MAP (High-resolution Informatics Toolbox in MALDI-MSI Proteomics), an open-source bioinformatics workflow using peptide mass fingerprint analysis and a dual scoring system to computationally assign peptide and protein annotations to high mass resolution MSI datasets and generate customisable spatial distribution maps. HIT-MAP will be a valuable resource for the spatial proteomics community for analysing newly generated and retrospective datasets, enabling robust peptide and protein annotation and visualisation in a wide array of normal and disease contexts. MALDI-mass spectrometry imaging (MSI) can reveal the distribution of proteins in tissues but tools for protein identification and annotation are sparse. Here, the authors develop an open-source bioinformatic workflow for false discovery rate-controlled protein annotation and spatial mapping from MALDI-MSI data.
引用
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页数:16
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