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

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.

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Publication Details

Journal
ACS Nano
Published
2025-03-20
DOI
https://doi.org/10.1021/acsnano.4c15538
Citations
5
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
4.03

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article

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

Lisa M. Utschig, Eric L. Hegg, Markus Sutter, Corie Y. Ralston et al.
5 citations
ACS Nano
Biochemical and Structural Characterization
4.03
article

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

Lisa M. Utschig, Eric L. Hegg, Markus Sutter, Corie Y. Ralston, Cheryl A. Kerfeld, Samuel N. Snyder, David M. Tiede, Xiaobing Zuo, Arinita Pramanik, T M Chiang, Kyleigh L. Range, Joel F. Landa
article en
5 citations

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.

ACS NanoVol. 19(12)
Argonne National Laboratory (US), Lawrence Berkeley National Laboratory (US), Institute of Molecular and Cell Biology (RU), Foundry (United Kingdom) (GB), Plant (United States) (US), Genomics (United Kingdom) (GB), Molecular Foundry, Michigan State University (US)
Basic Energy Sciences
Openalex Percentile: Top 7%
Biochemical and Structural Characterization
4.03
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