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


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
28 05 2021
Historique:
received: 06 10 2020
accepted: 29 04 2021
entrez: 29 5 2021
pubmed: 30 5 2021
medline: 9 6 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34050164
doi: 10.1038/s41467-021-23461-w
pii: 10.1038/s41467-021-23461-w
pmc: PMC8163805
doi:

Substances chimiques

Peptides 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3241

Subventions

Organisme : NEI NIH HHS
ID : R01 EY013462
Pays : United States

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Auteurs

G Guo (G)

Mass Spectrometry Hub, University of Auckland, Auckland, New Zealand.
School of Biological Sciences, University of Auckland, Auckland, New Zealand.

M Papanicolaou (M)

The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, UNSW Sydney, Sydney, NSW, Australia.
School of Life Sciences, University of Technology Sydney, Sydney, NSW, Australia.

N J Demarais (NJ)

Mass Spectrometry Hub, University of Auckland, Auckland, New Zealand.
University of Auckland, School of Biological Sciences, Auckland, New Zealand.

Z Wang (Z)

Department of Biochemistry, Vanderbilt University, Nashville, TN, USA.

K L Schey (KL)

Department of Biochemistry, Vanderbilt University, Nashville, TN, USA.

P Timpson (P)

The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, UNSW Sydney, Sydney, NSW, Australia.
St Vincent's Clinical School, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia.

T R Cox (TR)

The Garvan Institute of Medical Research and The Kinghorn Cancer Centre, UNSW Sydney, Sydney, NSW, Australia. t.cox@garvan.org.au.
St Vincent's Clinical School, Faculty of Medicine, UNSW Sydney, Sydney, NSW, Australia. t.cox@garvan.org.au.

A C Grey (AC)

Mass Spectrometry Hub, University of Auckland, Auckland, New Zealand. ac.grey@auckland.ac.nz.
School of Biological Sciences, University of Auckland, Auckland, New Zealand. ac.grey@auckland.ac.nz.

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Classifications MeSH