Covalent Inhibition of a Host-Pathogen Protein-Protein Interaction Reduces the Infectivity of <i>Streptococcus pneumoniae</i>.

ABSTRACT: The ever-expanding antibiotic resistance urgently calls for novel antibacterial therapeutics, especially those with a new mode of action. We report herein our exploration of protein-protein interaction (PPI) inhibition as a new mechanism to thwart bacterial pathogenesis. Specifically, we describe potent and specific inhibitors of the pneumococcal surface protein PspC, an important virulence factor that facilitates the infection of Streptococcus pneumoniae. Specifically, PspC has been documented to recruit human complement factor H (hFH) to suppress host complement activation and/or promote the bacterial attachment to host tissues. The CCP9 domain of hFH was recombinantly expressed to inhibit the PspC-hFH interaction as demonstrated on live pneumococcal cells. The inhibitor allowed f

SUBMITTER: Lyu Y 

PROVIDER: S-EPMC11267552 | biostudies-literature | 2024 Jul

REPOSITORIES: biostudies-literature