Document Type
Article
Journal/Book Title
Proteins
Publication Date
6-4-2019
Publisher
John Wiley & Sons, Inc.
Award Number
NIH 1R15AI124108-01A1
Funder
NIH
Volume
87
Issue
11
First Page
931
Last Page
942
Abstract
Like many Gram-negative pathogens, Shigella rely on a type three secretion system (T3SS) for injection of effector proteins directly into eukaryotic host cells to initiate and sustain infection. Protein secretion through the needle-like type three secretion apparatus (T3SA) requires ATP hydrolysis by the T3SS ATPase Spa47, making it a likely target for in vivo regulation of T3SS activity and an attractive target for small molecule therapeutics against shigellosis. Here, we developed a model of an activated Spa47 homo-hexamer, identifying two distinct regions at each protomer interface that we hypothesized to provide intermolecular interactions supportingSpa47 oligomerization and enzymatic activation. Mutational analysis and a series of high-resolution crystal structures confirm the importance of these residues, as many of the engineered mutants are unable to form oligomers and efficiently hydrolyze ATP in vitro. Furthermore, in vivo evaluation of Shigella virulence phenotype uncovered a strong correlation between T3SS effector protein secretion, host cell membrane disruption, and cellular invasion by the tested mutant strains, suggesting that perturbation of the identified interfacial residues/interactions influences Spa47 activity through preventing oligomer formation, which in turn regulates Shigella virulence. The most impactful mutations are observed within the conserved Site 2 interface where the native residues support oligomerization and likely contribute to a complex hydrogen bonding network that organizes the active site and supports catalysis. The critical reliance on these conserved residues suggests that aspects of T3SS regulation may also be conserved, providing promise for the development of a cross-species therapeutic that broadly targetsT3SS ATPase oligomerization and activation.
Recommended Citation
Demler, HJ, Case, HB, Morales, Y, Bernard, AR, Johnson, SJ, Dickenson, NE. Interfacial amino acids support Spa47 oligomerization and shigella type three secretion system activation. Proteins. 2019; 87: 931– 942. https://doi.org/10.1002/prot.25754
