Inhibitory proteins of Bacillus subtilis interact within the membrane to block intramembrane protease activity

TL;DR

This paper shows how inhibitory proteins in bacteria interact with a membrane protease to block its activity, which could help in developing new treatments.

Contribution

First experimental evidence of physical contacts between BofA and SpoIVFA in the membrane-bound inhibition complex of SpoIVFB.

Findings

BofA's C-terminal region is close to SpoIVFA's transmembrane segment in the inhibition complex.

BofA and SpoIVFA likely interact to block SpoIVFB's cleavage of Pro-σK during endosporulation.

Orthologs of BofA and SpoIVFA in pathogenic Bacilli may function similarly to inhibit virulence.

Abstract

Intramembrane proteases (IPs) are crucial for diverse signaling pathways, including some that regulate the virulence of pathogenic bacteria. A better understanding of mechanisms controlling IP activity is necessary to guide therapeutic development. Bacillus subtilis SpoIVFB is an IP with two natural inhibitory proteins, BofA and SpoIVFA. These proteins form a complex with SpoIVFB and prevent it from cleaving Pro-σK during endosporulation. We investigated proximity between BofA and SpoIVFA in the SpoIVFB inhibition complex using in vivo disulfide crosslinking in Escherichia coli. We discovered that two parts of the BofA C-terminal region are proximal to the SpoIVFA transmembrane segment (TMS). Our results support predictions that the BofA C-terminal region adopts an unusual structure within the membrane and interacts with the SpoIVFA TMS to block SpoIVFB cleavage of Pro-σK. Endospore-forming Bacilli, including several pathogenic species, encode BofA and SpoIVFA orthologs, which likely interact in a similar fashion to inhibit their SpoIVFB ortholog. It may be possible to control SpoIVFB activity and hence endosporulation with modulators that target the interaction between BofA and SpoIVFA.

Regulated intramembrane proteolysis (RIP) pathways govern important processes in all three domains of life. A key component of RIP pathways is an intramembrane protease (IP), which cleaves one or more substrates within a membrane. Developing modulators of IPs has been challenging, particularly for metallo-IPs. Bacterial metallo-IPs function in RIP pathways that control the virulence of many pathogens. SpoIVFB is a metallo-IP necessary for endosporulation of Bacillus subtilis. Endosporulation enhances the survival of pathogenic Bacilli, which encode orthologs of SpoIVFB and its natural inhibitory proteins BofA and SpoIVFA. Here, we present the first experimental evidence for contacts between BofA and SpoIVFA within the membrane-embedded SpoIVFB inhibition complex, providing foundations for a deeper understanding of mechanisms controlling metallo-IP activity.

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