Evidence map›Paper›PMID 39961049›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2025

Electrochemically Driven Optical Dynamics of Reflectin Protein Films.

Yin-Chen Lin, Changxuan Yang, Seren Tochikura, Joshua R Uzarski, Daniel E Morse, Lior Sepunaru, Michael J Gordon

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2025. 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

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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Electrochemically Driven Optical Dynamics of Reflectin Protein Films.Advanced materials (Deerfield Beach, Fla.) · 2025
    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

7 authors.

Yin-Chen LinInstitute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106, USA.
Changxuan YangDepartment of Chemical Engineering, University of California, Santa Barbara, CA, 93106, USA.
Seren TochikuraDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, CA, 93106, USA.
Joshua R UzarskiU.S. Army Combat Capabilities Development Command Soldier Center, 15 General Greene Avenue, Natick, MA, 01760, USA.
Daniel E MorseInstitute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106, USA.
Lior SepunaruDepartment of Chemistry and Biochemistry, University of California, Santa Barbara, CA, 93106, USA.
Michael J GordonInstitute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106, USA.ORCID https://orcid.org/0000-0003-0123-9649

Funding

Bioelectrochemistry at the Nanoscale: Fundamentals and ApplicationsR35GM142920 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SEPUNARU, LIOR · 2021 to 2025
$1.7M
Army Research Office W911NF-19-D-0001Army Research Office W911NF-21-2-0068NIGMS NIH HHS R35 GM142920NIH HHS R35GM142920
6 · The paper itself

Abstract

Neuronally triggered phosphorylation drives the dynamic condensation of reflectin proteins, enabling squid to fine tune the colors reflected from specialized skin cells (iridocytes) for camouflage and communication. Reflectin, the primary component of iridocyte lamellae, forms alternating layers of protein and low refractive index extracellular space within membrane-encapsulated structures, acting as a biologically tunable distributed Bragg reflector. In vivo, reflectin condensation induces osmotic dehydration of these lamellae, reducing their thickness and shifting the wavelength of reflected light. Inspired by this natural mechanism, we demonstrate that electrochemical reduction of imidazolium moieties within the protein provides a reversible and tunable method to control the water volume fraction in reflectin thin films, allowing precise, dynamic modulation of the film's refractive index and thickness - mimicking the squid's dynamic color adaptation. To unravel the underlying mechanisms, we developed electrochemical correlative ellipsometry and surface plasmon resonance spectroscopy, enabling real-time analysis of optical property changes of reflectin films. This electrochemically driven approach offers unprecedented control over reflectin condensation dynamics. Our findings not only deepen the understanding of biophysical processes governing cephalopod coloration but also pave the way for bio-inspired materials and devices that seamlessly integrate biological principles with synthetic systems to bridge the biotic-abiotic gap.

Indexed as

Electrochemical TechniquesOptical PhenomenaProteinsAnimalsDecapodiformesSurface Plasmon ResonanceProteinselectrochemistryellipsometryreflectinsurface plasmon resonance

Identifiers

PMID39961049
PMCPMC11937991

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Registered trials

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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.