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Biology subjects

Karimova, G.

Publications and source records attributed to Karimova, G..

2 recordsLinked to original sources

Structure-guided generative design of peptides targeting the FtsQBL divisome complex inhibit Escherichia coli cell division.

The discovery of antibiotics targeting Gram-negative bacteria remains limited in part by the difficulty of pharmacologically modulating protein-protein interactions essential for bacterial physiology. The divisome complex formed by FtsQ, FtsB and FtsL represents an attractive but challenging target, as its assembly relies on {beta}-strand-mediated interface interactions within the bacterial periplasm. Here, we combined interpretable interface mapping using InDeep with hotspot-constrained RFdiffusion design to generate peptides targeting the FtsB-binding site of Escherichia coli FtsQ. The designed peptides mimic the native {beta}-augmentation interaction and selectively engage the FtsQ interface both in bacterial cells and in vitro. X-ray crystallography of one of these peptides in complex with FtsQ reveals that it accurately adopts the native binding geometry while introducing additional stabilizing interactions within a hydrophobic pocket. Complementary NMR analyses further show that optimized peptides adopt pre-organized {beta}-hairpin conformations in solution consistent with the bound state. Several of these peptides disrupt bacterial cell division and inhibit growth in an E. coli strain exhibiting increased outer membrane permeability. Together, these results establish a structurally validated framework in which predictive interface analysis and generative design can be combined to target cooperative protein-protein interfaces in bacteria and provide a foundation for the development of divisome-targeting antibacterial strategies.

microbiology↗

Exploring the multi-protein assembly of the enzymes of the de novo purine nucleotide biosynthetic pathway from Pseudomonas aeruginosa

Purine nucleotide biosynthesis is a crucial metabolic pathway responsible that produces building blocks essential for a plethora of cellular processes. In bacteria, the de novo purine nucleotide biosynthetic pathway (DNPNB) involves fifteen chemical steps catalysed by fourteen different enzymes. While the mammalian orthologues have been extensively shown to interact and form a metabolon named "purinosome", the possible existence of a prokaryotic equivalent was only recently revealed for the case of Escherichia coli. In this study, we explored the potential conservation of a bacterial purinosome-like complex in Pseudomonas aeruginosa, an opportunistic pathogen known for its high antibiotic resistance. Using a bacterial two-hybrid system, we mapped protein-protein interactions among all tested DNPNB enzymes in P. aeruginosa and revealed a dense interaction network. An in-silico protein-protein docking approach on three core enzymes allowed the structural reconstitution of a complex composed of PurK, PurE and PurC with a 4:8:8 stoichiometry, respectively. Interestingly, a tunnel connecting the different active sites has been revealed, showing a metabolon-like property for possible efficient substrate channelling. These findings support a conserved regulatory organization of purine biosynthesis in bacteria, providing deeper insights into bacterial metabolism and paving the way for potential antibiotic targets.

biochemistry↗