Abstract
All human diseases involve proteins, yet our current tools to characterize and quantify them are limited. To better elucidate proteins across space, time, and molecular composition, we provide a >10 years of projection for technologies to meet the challenges that protein biology presents. With a broad perspective, we discuss grand opportunities to transition the science of proteomics into a more propulsive enterprise. Extrapolating recent trends, we describe a next generation of approaches to define, quantify, and visualize the multiple dimensions of the proteome, thereby transforming our understanding and interactions with human disease in the coming decade.
Original language | English (US) |
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Article number | 100254 |
Journal | Molecular and Cellular Proteomics |
Volume | 21 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2022 |
Funding
Funding and additional information—C. V. was supported by awards R35GM127089, 75N93019C00052, and the Chan Zuckerberg Initiative; K. E. B.-J. was supported by award UH3 CA255132-03; N. L. K. by UH3 CA246635-02; G. P. N. by U54 HG010426-03; and J. M. S. U54 DK120058-03, all of which are part of the Human Biomolecular Atlas Program. A. N. was supported by R01 CA232517 and Catalyst Award C-088 from the Chicago Biomedical Consortium, United States. A. E. H. was supported by a National Institutes of Health Cancer Moonshot, United States grant (grant no.: R33CA225296) and as a Chan Zuckerberg Biohub Investigator. E. L. was supported by the KAW Foundation (grant nos.: 2016.0204 and 2018.0172), the Swedish Research Council, Sweden (grant no.: 2017-05327), and the Chan Zuckerberg Initiative, United States (grant no.: CZF2019-002448). N. S. was supported by DP2GM123497 and CZF2019-002424, and N. S. and N. L. K. were supported by Allen Distinguished Investigator awards through the Paul G. Allen Frontiers Group. R. T. K. was supported by R01 GM138931.
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Molecular Biology