Evidence map›Paper›PMID 40113598›Full record

ArticleACS nano2025

Chaotrope-Based Approach for Rapid In Vitro Assembly and Loading of Bacterial Microcompartment Shells.

Kyleigh L Range, Timothy K Chiang, Arinita Pramanik, Joel F Landa, Samuel N Snyder, Xiaobing Zuo, David M Tiede, Lisa M Utschig, Eric L Hegg, Markus Sutter and 2 more

Abstract read
In one paragraph

Article in ACS nano, 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. 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

12 authors.

Kyleigh L RangeMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824, United States.ORCID 0009-0009-4333-7539
Timothy K ChiangMolecular Foundry Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0009-0000-5811-9221
Arinita PramanikMolecular Foundry Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Joel F LandaCell and Molecular Biology Department, Michigan State University, East Lansing, Michigan 48824, United States.ORCID 0000-0003-1882-6698
Samuel N SnyderChemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.ORCID 0000-0002-2571-4048
Xiaobing ZuoX-ray Science Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.
David M TiedeChemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.ORCID 0000-0002-2784-4954
Lisa M UtschigChemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, Illinois 60439, United States.ORCID 0000-0003-2095-5392
Eric L HeggCell and Molecular Biology Department, Michigan State University, East Lansing, Michigan 48824, United States.ORCID 0000-0003-2055-5495
Markus SutterMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824, United States.ORCID 0000-0001-6290-4820
Cheryl A KerfeldMSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824, United States.ORCID 0000-0002-9977-8482
Corie Y RalstonMolecular Foundry Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.ORCID 0000-0002-7899-0951

Funding

X-ray Scattering Technology CoreP30GM133893 · NIGMS · BROOKHAVEN SCIENCE ASSOC-BROOKHAVEN LAB · PI Sean McSweeney · 2019 to 2026
$38.6M
A Simultaneous SAXS/WAXS Detector System for Solving Biological StructuresS10OD012331 · OD · STATE UNIVERSITY NEW YORK STONY BROOK · PI ALLAIRE, MARC · 2012 to 2012
$1.1M
NIGMS NIH HHS P30 GM133893NIH HHS S10 OD012331
6 · The paper itself

Abstract

Bacterial microcompartments (BMCs) are proteinaceous organelles that self-assemble into selectively permeable shells that encapsulate enzymatic cargo. BMCs enhance catalytic pathways by reducing crosstalk among metabolites, preventing harmful intermediates from leaking into the cytosol and increasing reaction efficiency via enzyme colocalization. The intrinsic properties of BMCs make them attractive for biotechnological engineering. However, in vivo expression methods for shell synthesis have significant drawbacks that limit the potential design space for these nanocompartments. Here, we describe the development of an efficient and rapid method for the in vitro assembly of BMC shells from their protein building blocks. Our method enables large-scale construction of BMC shells by utilizing urea as a chaotropic agent to control self-assembly and provides an approach for encapsulation of both biotic and abiotic cargo under a broad range of reaction conditions. We demonstrate an enhanced level of control over the assembly of BMC shells in vitro and expand the design parameter space for engineering BMC systems with specialized and enhanced catalytic properties.

Indexed as

BacteriaBacterial ProteinsOrganellesUreaBacterial ProteinsUreabacterial microcompartmentsbiotic and abiotic cargo encapsulationcatalysisconfinementin vitroself-assemblyurea

Identifiers

PMID40113598
PMCPMC11966763

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.