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Biology subjects

Giudice, E.

Publications and source records attributed to Giudice, E..

3 recordsLinked to original sources

HInt: interaction-based homology discovery through accelerated genome-scale AlphaFold screening

Identifying homologous proteins across deep evolutionary distances remains a major challenge because sequence and structural similarity progressively become undetectable over time. Although protein-protein interactions (PPIs) are often constrained by function and evolution, whether conserved interaction interfaces can provide an independent signal for homology detection has remained largely unexplored owing to the computational cost of proteome-scale interaction prediction. Here we introduce HInt (Homology by Interaction), an accelerated AlphaFold-based framework that enables practical proteome-scale PPI prediction through biologically informed pre-filtering and optimised high-throughput structure modelling. Using HInt, we establish interaction-based similarity as a third axis of homology detection. We show that conserved interaction interfaces reveal homologous relationships that remain inaccessible to conventional sequence- and structure-based approaches. Application of HInt to both prokaryotic and eukaryotic systems, together with experimental validation, uncovered a previously unrecognised VirB5 pilus-tip protein in the F-plasmid type IV secretion system and a previously unannotated F-box-like protein in the Saccharomyces cerevisiae ubiquitin-proteasome system. By enabling practical proteome-scale interaction screening, HInt provides a general framework for uncovering hidden homologues and expands the conceptual landscape of protein homology inference.

molecular biology↗

Structural characterization of hibernating ribosomes in four Gram-negative pathogenic bacteria

Ribosomes are universal molecular machines that translate messenger RNA into proteins. Depending on what the cells needs for protein synthesis, ribosomes exist in various functional states, and when cells face stressful conditions, their ribosomes may enter into an inactive hibernation state. In bacteria, this ability to become dormant through ribosomal hibernation plays a crucial role in their survival, especially when the cells are targeted by ribosome-targeting antibiotics. The phenomenon occurs when ribosomes bind with hibernation factors. In this work, we examine how these special proteins interact with ribosomes from four different Gram-negative pathogens, and how this leads to translation inhibition, reporting the single-particle cryo-electron microscopy structures of hibernating ribosomes from P. aeruginosa, E. hormaechei, K. quasipneumoniae, and A. baumannii. We show that these ribosomal complexes contain either short HPF or YfiA tightly bound to the 30S A-site, P-site, and even occasionally to the E-site. Our results provide valuable insights into the ribosomal hibernation mechanism, paving the way to both a better understanding of bacterial dormancy and the possibility of developing antibiotics which will target hibernating ribosomes rather than just active ones.

biochemistry↗

PPIFold: A Tool for Analysis of Protein-Protein Interaction from AlphaPullDown

Protein structure and protein-protein interaction (PPI) predictions based on coevolution have transformed structural biology, but managing pre-processing and post-processing can be complex and time-consuming, making these tools less accessible. Here, we introduce PPIFold, a pipeline built on the AlphaPulldown Python package, designed to automate file handling and streamline the generation of outputs, facilitating the interpretation of PPI prediction results. The pipeline was validated on the bacterial Type 4 Secretion System nanomachine, demonstrating its effectiveness in simplifying PPI analysis and enhancing accessibility for researchers.

bioinformatics↗