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Protein surface chemistry encodes an adaptive tolerance to desiccation
Open accessPreprint — published as 10.1016/j.cels.2025.101407 · Paper page
Abstract
Cellular desiccation - the loss of nearly all water from the cell - is a recurring stress in an increasing number of ecosystems that can drive protein unfolding and aggregation. For cells to survive, at least some of the proteome must resume function upon rehydration. Which proteins tolerate desiccation, and the molecular determinants that underlie this tolerance, are largely unknown. Here, we apply quantitative and structural proteomic mass spectrometry to show that certain proteins possess an innate capacity to tolerate rehydration following extreme water loss. Structural analysis points to protein surface chemistry as a key determinant for desiccation tolerance, which we test by showing that rational surface mutants can convert a desiccation sensitive protein into a tolerant one. Desiccation tolerance also has strong overlap with cellular function, with highly tolerant proteins responsible for production of small molecule building blocks, and intolerant proteins involved in energy-consuming processes such as ribosome biogenesis. As a result, the rehydrated proteome is preferentially enriched with metabolite and small molecule producers and depleted of some of the cell’s heaviest consumers. We propose this functional bias enables cells to kickstart their metabolism and promote cell survival following desiccation and rehydration. Teaser: Proteins can resist extreme dryness by tuning the amino acids on their surfaces.
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Metadata
- Authors
- Romero-Pérez, P. S., Moran, H. M., Horani, A., Truong, A., Manriquez-Sandoval, E., Ramirez, J. F., Martinez, A., Gollub, E., Hunter, K., Lotthammer, J. M., Emenecker, R. J., Liu, H., Iwasa, J. H., Boothby, T. C., Holehouse, A. S., Fried, S. D., & Sukenik, S.
- Affiliations
- Johns Hopkins University (US)
- University of California, Merced (US)
- University of Wyoming (US)
- Washington University in St. Louis (US)
- University of Utah (US)
- Corresponding author
- Holehouse, Alex S.
- Fried, Stephen D.
- Sukenik, Shahar
- ORCID
- Venue
- Cell Systems
- Publisher
- openRxiv
- Published
- 2024-07-29
- Volume
- 16
- Issue
- 10
- Pages
- 101407-101407
- ISSN
- 2405-4712 (ISSN-L)
- PMC
- PMC11312438
- OpenAlex
- W4414805570
- Cited by
- 9
- References
- 1
- Citations by year
- 2026: 5 · 2025: 4
- FWCI
- 1.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cell Systems (acceptedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- SSRN Electronic Journal (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- Funders
- National Science Foundation (2213983, 2045844, 2128067, 2128068, CAREER, 1817845, 2139839, 2128069)
- Alfred P. Sloan Foundation
- Human Frontier Science Program (RGP0015/2022)
- National Institutes of Health (1dp2gm140926-01)
- National Institute of General Medical Sciences (DP2-GM140926, T32GM080189, T32GM135131)
- Division of Biological Infrastructure (62937, 89249, 89248, 89252, 2213983, 89247, CAREER, 62936, 1817845)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Tardigrade Biology and Ecology
- Keywords
- desiccation tolerance, rehydration, protein stability, ribosome biogenesis
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