First-pass extracted concept

stochastic self-assembly

Candidate: concept label1 source documents4 linked claims
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What the tool is doing

This is the mechanistic interpretation proposed for how chemotaxis clusters form and are maintained. The paper argues that stochastic self-assembly can generate approximately periodic membrane structures without direct cytoskeletal involvement or active transport.

Source 1DOIPubMed

Evidence Snippets

Analysis of the relative cellular locations of 1.1 million individual proteins (from 326 cells) suggests that clusters form via stochastic self-assembly.
Evidence 1Source 1DOIPubMedprovenance

Supporting Sources

Linked Claims

Claim 1distribution observationsupports2009Source 1DOIPubMed

Chemotaxis cluster sizes are approximately exponentially distributed and lack a characteristic cluster size.

Quoted textsource-backed
We find that cluster sizes are approximately exponentially distributed, with no characteristic cluster size.
Claim 2localization fractionsupports2009Source 1DOIPubMed

About one-third of Tar receptors are in smaller lateral clusters rather than large polar clusters.

Quoted textsource-backed
One-third of Tar receptors are part of smaller lateral clusters and not of the large polar clusters.
Claim 3mechanistic inferencesupports2009Source 1DOIPubMed

Analysis of 1.1 million individual protein localizations from 326 cells suggests that chemotaxis clusters form via stochastic self-assembly.

Quoted textsource-backed
Analysis of the relative cellular locations of 1.1 million individual proteins (from 326 cells) suggests that clusters form via stochastic self-assembly.
Claim 4mechanistic model supportsupports2009Source 1DOIPubMed

Super-resolution PALM maps support that stochastic self-assembly can create and maintain approximately periodic membrane structures without direct cytoskeletal involvement or active transport.

Quoted textsource-backed
The super-resolution PALM maps of E. coli receptors support the notion that stochastic self-assembly can create and maintain approximately periodic structures in biological membranes, without direct cytoskeletal involvement or active transport.