Evidence map›Paper›PMID 40521613›Full record

ReviewProtein science : a publication of the Protein Society2025

Biomolecular condensates-Prerequisites for anhydrobiosis?

Charles A Elder, Hannah M Skaggs, Lynnette M A Dirk, David F Grimm, Clinton J Belott, Willem F Wolkers, Harriëtte Oldenhof, Vladimir N Uversky, A Bruce Downie, Michael A Menze

Abstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Principles Underlying Cryopreservation and Freeze-Drying of Cells.Methods in molecular biology (Clifton, N.J.) · 2026
    Review
  4. Review
  5. Biomolecular condensates-Prerequisites for anhydrobiosis?Protein science : a publication of the Protein Society · 2025
    Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Charles A ElderDepartment of Biology, University of Louisville, Louisville, Kentucky, USA.ORCID 0009-0004-3137-4096
Hannah M SkaggsDepartment of Biology, University of Louisville, Louisville, Kentucky, USA.
Lynnette M A DirkSeed Biology Group, Department of Horticulture, Martin-Gatton College of Agriculture, Food and Environment, University of Kentucky, Lexington, Kentucky, USA.ORCID 0000-0002-7564-5095
David F GrimmDepartment of Biology, University of Louisville, Louisville, Kentucky, USA.
Clinton J BelottDepartment of Biology, University of Louisville, Louisville, Kentucky, USA.
Willem F WolkersBiostabilization Laboratory-Lower Saxony Centre for Biomedical Engineering, Implant Research and Development, Hannover, Germany.
Harriëtte OldenhofBiostabilization Laboratory-Lower Saxony Centre for Biomedical Engineering, Implant Research and Development, Hannover, Germany.
Vladimir N UverskyDepartment of Molecular Medicine and USF Health Byrd Alzheimer's Research Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
A Bruce DownieSeed Biology Group, Department of Horticulture, Martin-Gatton College of Agriculture, Food and Environment, University of Kentucky, Lexington, Kentucky, USA.ORCID 0000-0001-6680-0551
Michael A MenzeDepartment of Biology, University of Louisville, Louisville, Kentucky, USA.ORCID 0000-0003-1072-5462

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is often underappreciated that despite water being a requirement for life on Earth, organisms belonging to all taxonomic kingdoms have developed mechanisms to survive desiccation. These organisms, referred to as anhydrobiotes, accumulate specific biomolecules during or before drying that facilitate the survival of desiccation stress. Compounds utilized by a wide variety of anhydrobiotes during desiccation include metabolites such as sugars and amino acids, as well as proteins with extensive intrinsically disordered regions. Intrinsically disordered proteins that are constitutively expressed or upregulated during the onset or in preparation for desiccation include late embryogenesis abundant proteins, tardigrade disordered proteins, hydrophilins, some small heat shock proteins, and prion-like proteins. Some of these proteins form biomolecular condensates in the cellular environment. We hypothesize that phase transitions driven by anhydrobiosis-related intrinsically disordered proteins play a substantial role in enabling anhydrobiosis by (1) contributing to the downregulation of metabolic and developmental processes, (2) selectively sequestering desiccation-sensitive molecules into a "protective compartment" during drying, (3) interfering with programmed cell death signaling pathways to confer optimal time for the cell to repair after rehydration, (4) resisting intracellular volume changes to aid in membrane stabilization during desiccation, and (5) changing the biophysical properties of water to reduce desiccation-induced cellular damage. Biochemical strategies in anhydrobiotes are certainly multifaceted and may differ among systems. Nevertheless, a better understanding of the relevance of phase transitions in anhydrobiosis may allow us to get one step closer to unraveling the enigmatic phenomenon of life without water.

Indexed as

Biomolecular CondensatesIntrinsically Disordered ProteinsAnimalsDesiccationTardigradaIntrinsically Disordered Proteinscryptobiosisintrinsically disordered proteinsliquid–liquid phase separationmembraneless organellesstress tolerance

Identifiers

PMID40521613
PMCPMC12168135

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.