Evidence map›Paper›PMID 35914159›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Controlling the shape and topology of two-component colloidal membranes.

Ayantika Khanra, Leroy L Jia, Noah P Mitchell, Andrew Balchunas, Robert A Pelcovits, Thomas R Powers, Zvonimir Dogic, Prerna Sharma

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 59% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Topology and kinetic pathways of colloidosome assembly and disassembly.Proceedings of the National Academy of Sciences of the United States of America · 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

8 authors at 5 institutions in 2 countries.

Ayantika KhanraDepartment of Physics, Indian Institute of Science, Bangalore 560012, India.ORCID 0000-0002-8550-9142
Leroy L JiaCenter for Computational Biology, Flatiron Institute, New York, NY 10010.ORCID 0000-0003-1968-4767
Noah P MitchellKavli Institute for Theoretical Physics, University of California, Santa Barbara, CA 93106.ORCID 0000-0003-1922-8470
Andrew BalchunasMartin A. Fisher School of Physics, Brandeis University, Waltham, MA 02454.
Robert A PelcovitsBrown Theoretical Physics Center and Department of Physics, Brown University, Providence, RI 02912.
Thomas R PowersBrown Theoretical Physics Center and Department of Physics, Brown University, Providence, RI 02912.ORCID 0000-0003-3432-8226
Zvonimir DogicPhysics Department, University of California, Santa Barbara, CA 93106.ORCID 0000-0003-0142-1838
Prerna SharmaDepartment of Physics, Indian Institute of Science, Bangalore 560012, India.ORCID 0000-0003-4988-9560
Brown University · USIndian Institute of Science Bangalore · INUniversity of California, Santa Barbara · USBrandeis University · USFlatiron Health (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Changes in the geometry and topology of self-assembled membranes underlie diverse processes across cellular biology and engineering. Similar to lipid bilayers, monolayer colloidal membranes have in-plane fluid-like dynamics and out-of-plane bending elasticity. Their open edges and micrometer-length scale provide a tractable system to study the equilibrium energetics and dynamic pathways of membrane assembly and reconfiguration. Here, we find that doping colloidal membranes with short miscible rods transforms disk-shaped membranes into saddle-shaped surfaces with complex edge structures. The saddle-shaped membranes are well approximated by Enneper's minimal surfaces. Theoretical modeling demonstrates that their formation is driven by increasing the positive Gaussian modulus, which in turn, is controlled by the fraction of short rods. Further coalescence of saddle-shaped surfaces leads to diverse topologically distinct structures, including shapes similar to catenoids, trinoids, four-noids, and higher-order structures. At long timescales, we observe the formation of a system-spanning, sponge-like phase. The unique features of colloidal membranes reveal the topological transformations that accompany coalescence pathways in real time. We enhance the functionality of these membranes by making their shape responsive to external stimuli. Our results demonstrate a pathway toward control of thin elastic sheets' shape and topology-a pathway driven by the emergent elasticity induced by compositional heterogeneity.

Indexed as

Lipid BilayersElasticityMembranesNormal DistributionLipid Bilayersmembranesminimal surfacestopological shape transitions

Identifiers

PMID35914159
PMCPMC9371715
OpenAlexW4221144493

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.