4.7 Article

Self-assembling Shell Proteins PduA and PduJ have Essential and Redundant Roles in Bacterial Microcompartment Assembly

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 433, Issue 2, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2020.11.020

Keywords

1,2-propanediol utilization MCP; gene knockout; oligomerization; Salmonella enterica serovar Typhimurium LT2; rapid self-assembly assay

Funding

  1. National Science Foundation [MCB1150567]
  2. Army Research Office [W911NF-19-1-0298]
  3. Department of Energy [DESC0019337]
  4. National Science Foundation Graduate Research Fellowship Program through Northwestern University's Biotechnology Training Program [DGE-1842165]
  5. National Institutes of Health Training Grant through Northwestern University's Biotechnology Training Program [T32GM008449]
  6. Summer Undergraduate Research Grant though the Office of Undergraduate Research at Northwestern University [586SUMMER1812972]
  7. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF ECCS-1542205]
  8. MRSEC program at the Materials Research Center [NSF DMR-1720139]
  9. International Institute for Nanotechnology (IIN)
  10. Keck Foundation
  11. State of Illinois, through the IIN

Ask authors/readers for more resources

Protein self-assembly is a common and essential biological phenomenon, and bacterial microcompartments serve as a promising model system for studying this process. The shell proteins PduA and PduJ are essential for the assembly of bacterial microcompartments, with at least one of them required for shell formation.
Protein self-assembly is a common and essential biological phenomenon, and bacterial microcompartments present a promising model system to study this process. Bacterial microcompartments are large, protein-based organelles which natively carry out processes important for carbon fixation in cyanobacteria and the survival of enteric bacteria. These structures are increasingly popular with biological engineers due to their potential utility as nanobioreactors or drug delivery vehicles. However, the limited understanding of the assembly mechanism of these bacterial microcompartments hinders efforts to repurpose them for non-native functions. Here, we comprehensively investigate proteins involved in the assembly of the 1,2-propanediol utilization bacterial microcompartment from Salmonella enterica serovar Typhimurium LT2, one of the most widely studied microcompartment systems. We first demonstrate that two shell proteins, PduA and PduJ, have a high propensity for self-assembly upon overexpression, and we provide a novel method for self-assembly quantification. Using genomic knock-outs and knock-ins, we systematically show that these two proteins play an essential and redundant role in bacterial microcompartment assembly that cannot be compensated by other shell proteins. At least one of the two proteins PduA and PduJ must be present for the bacterial microcompartment shell to assemble. We also demonstrate that assembly-deficient variants of these proteins are unable to rescue microcompartment formation, highlighting the importance of this assembly property. Our work provides insight into the assembly mechanism of these bacterial organelles and will aid downstream engineering efforts. (C) 2020 Elsevier Ltd. All rights reserved.

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