Paulo Martel

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Assistant Professor

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About

Paulo Martel is an Assistant Professor at the University of the Algarve, Portugal. His research focuses on protein disulfide isomerase activity, the RofA regulon in Streptococcus pyogenes, and the FOXO family isoforms. His recent publications reflect a commitment to understanding molecular mechanisms and genetic regulation in bacterial pathogens.

Recent Grants

Grant: Close

Implementation of a Constant-pH Molecular Dynamics Simulation Protocol for proteins and its application to the study of the binding of the SARS-CoV-2 S S-protein to the ACE2 human protein receptor

Open Date: 2024-01-01

Close Date: 2024-01-01

Grant: Close

Implementation of a Constant-pH Molecular Dynamics Simulation Protocol for proteins and its application to the study of the binding of the SARS-CoV-2 S S-protein to the ACE2 human protein receptor

Open Date: 2024-01-01

Close Date: 2024-01-01

Grant: Open

Search for molecular modulators of Foxo3a activity

Open Date: 2023-03-01

Close Date: 2033-09-30

Grant: Close

A Biophysical Approach to Oxidative Protein Folding in the ER: Relative Importance of Ero1 and Prdx4 alternative pathways

Open Date: 2012-02-01

Close Date: 2015-04-30

Grant: Close

A Biophysical Approach to Oxidative Protein Folding in the ER: Relative Importance of Ero1 and Prdx4 alternative pathways

Open Date: 2012-02-01

Close Date: 2015-04-01

Articles (3)

Year:

2024

The standalone regulator RofA is a positive regulator of the pilus locus in Streptococcus pyogenes . Found in only certain emm genotypes, RofA has been reported to regulate other virulence factors, although its role in the globally dominant emm 1 S. pyogenes is unclear. Given the recent emergence of a new emm 1 (M1 UK ) toxigenic lineage that is distinguished by three non-synonymous SNPs in rofA , we characterized the rofA regulon in six emm 1 strains that are representative of the two contemporary major emm 1 lineages (M1 global and M1 UK ) using RNAseq analysis, and then determined the specific role of the M1 UK -specific rofA SNPs. Deletion of rofA in three M1 global strains led to altered expression of 14 genes, including six non-pilus locus genes. In M1 UK strains, deletion of rofA led to altered expression of 16 genes, including nine genes that were unique to M1 UK . Only the pilus locus genes were common to the RofA regulons of both lineages, while transcriptomic changes varied between strains even within the same lineage. Although introduction of the three SNPs into rofA did not impact gene expression in an M1 global strain, reversal of three SNPs in an M1 UK strain led to an unexpected number of transcriptomic changes that in part recapitulated transcriptomic changes seen when deleting RofA in the same strain. Computational analysis predicted that interactions with a key histidine residue in the PRD domain of RofA would differ between M1 UK and M1 global . RofA is a positive regulator of the pilus locus in all emm 1 strains but effects on other genes are strain- and lineage-specific, with no clear, common DNA binding motif. The SNPs in rofA that characterize M1 UK may impact regulation of RofA; whether they alter phosphorylation of the RofA PRD domain requires further investigation.

Year:

2023

Year:

2023

Collaborators (2)

Shiranee Sriskandan

Prof

Imperial College London

UNITED KINGDOM
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Eduardo Pinho Melo

Associate Professor

Universidade do Algarve

PORTUGAL
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