Evidence map›Paper›PMID 38427377›Full record

ArticleACS applied bio materials2024

Design and Construction of a Multi-Tiered Minimal Actin Cortex for Structural Support in Lipid Bilayer Applications.

Amanda J Smith, Theodore R B Larsen, Harmony K Zimmerman, Samuel J Virolainen, Joshua J Meyer, Lisa M Keranen Burden, Daniel L Burden

Abstract read
In one paragraph

Article in ACS applied bio materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Amanda J SmithChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.ORCID 0000-0003-3678-1104
Theodore R B LarsenChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.
Harmony K ZimmermanChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.
Samuel J VirolainenChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.
Joshua J MeyerChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.
Lisa M Keranen BurdenChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.
Daniel L BurdenChemistry Department, Wheaton College, 501 College Ave., Wheaton, Illinois 60187, United States.ORCID 0000-0001-9789-1572

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Artificial lipid bilayers have revolutionized biochemical and biophysical research by providing a versatile interface to study aspects of cell membranes and membrane-bound processes in a controlled environment. Artificial bilayers also play a central role in numerous biosensing applications, form the foundational interface for liposomal drug delivery, and provide a vital structure for the development of synthetic cells. But unlike the envelope in many living cells, artificial bilayers can be mechanically fragile. Here, we develop prototype scaffolds for artificial bilayers made from multiple chemically linked tiers of actin filaments that can be bonded to lipid headgroups. We call the interlinked and layered assembly a multiple minimal actin cortex (multi-MAC). Construction of multi-MACs has the potential to significantly increase the bilayer's resistance to applied stress while retaining many desirable physical and chemical properties that are characteristic of lipid bilayers. Furthermore, the linking chemistry of multi-MACs is generalizable and can be applied almost anywhere lipid bilayers are important. This work describes a filament-by-filament approach to multi-MAC assembly that produces distinct 2D and 3D architectures. The nature of the structure depends on a combination of the underlying chemical conditions. Using fluorescence imaging techniques in model planar bilayers, we explore how multi-MACs vary with electrostatic charge, assembly time, ionic strength, and type of chemical linker. We also assess how the presence of a multi-MAC alters the underlying lateral diffusion of lipids and investigate the ability of multi-MACs to withstand exposure to shear stress.

Indexed as

ActinsLipid BilayersActin CytoskeletonCell MembraneCytoskeletonActinsLipid Bilayersactinbiomembranelayer-by-layerlipid bilayernanopore Biosensorspolyelectrolytereconstitutionsurface dynamics

Identifiers

PMID38427377
PMCPMC10951949

What OpenQuestion holds

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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.