Evidence map›Paper›PMID 38965780›Full record

ArticleBiophysical journal2024

A colloidal model for the equilibrium assembly and liquid-liquid phase separation of the reflectin A1 protein.

Tse-Chiang Huang, Robert Levenson, Youli Li, Phillip Kohl, Daniel E Morse, M Scott Shell, Matthew E Helgeson

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Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

7 authors.

Tse-Chiang HuangDepartment of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California.
Robert LevensonLife Sciences, Soka University of America, Aliso Viejo, California.
Youli LiMaterials Research Laboratory, University of California Santa Barbara, Santa Barbara, California.
Phillip KohlMaterials Research Laboratory, University of California Santa Barbara, Santa Barbara, California.
Daniel E MorseDepartment of Molecular, Cellular, and Developmental Biology, University of California Santa Barbara, Santa Barbara, California.
M Scott ShellDepartment of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California. Electronic address: shell@ucsb.edu.
Matthew E HelgesonDepartment of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California. Electronic address: helgeson@ucsb.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reflectin is an intrinsically disordered protein known for its ability to modulate the biophotonic camouflage of cephalopods based on its assembly-induced osmotic properties. Its reversible self-assembly into discrete, size-controlled clusters and condensed droplets are known to depend sensitively on the net protein charge, making reflectin stimuli-responsive to pH, phosphorylation, and electric fields. Despite considerable efforts to characterize this behavior, the detailed physical mechanisms of reflectin's assembly are not yet fully understood. Here, we pursue a coarse-grained molecular understanding of reflectin assembly using a combination of experiments and simulations. We hypothesize that reflectin assembly and phase behavior can be explained from a remarkably simple colloidal model whereby individual protein monomers effectively interact via a short-range attractive and long-range repulsive (SA-LR) pair potential. We parameterize a coarse-grained SA-LR interaction potential for reflectin A1 from small-angle x-ray scattering measurements, and then extend it to a range of pH values using Gouy-Chapman theory to model monomer-monomer electrostatic interactions. The pH-dependent SA-LR interaction is then used in molecular dynamics simulations of reflectin assembly, which successfully capture a number of qualitative features of reflectin, including pH-dependent formation of discrete-sized nanoclusters and liquid-liquid phase separation at high pH, resulting in a putative phase diagram for reflectin. Importantly, we find that at low pH size-controlled reflectin clusters are equilibrium assemblies, which dynamically exchange protein monomers to maintain an equilibrium size distribution. These findings provide a mechanistic understanding of the equilibrium assembly of reflectin, and suggest that colloidal-scale models capture key driving forces and interactions to explain thermodynamic aspects of native reflectin behavior. Furthermore, the success of SA-LR interactions presented in this study demonstrates the potential of a colloidal interpretation of interactions and phenomena in a range of intrinsically disordered proteins.

Indexed as

ColloidsAnimalsHydrogen-Ion ConcentrationIntrinsically Disordered ProteinsModels, MolecularMolecular Dynamics SimulationPhase SeparationStatic ElectricityColloidsIntrinsically Disordered Proteins

Identifiers

PMID38965780
PMCPMC11427776

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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.