Biochemical evidences for M1-, M17- and M18-like aminopeptidases in marine invertebrates from Cuban coastline
-
Isel Pascual Alonso
, Laura Rivera Méndez
, Mario E. Valdés-Tresanco
, Lotfi Bounaadja , Marjorie Schmitt , Yarini Arrebola Sánchez , Luis Alvarez Lajonchere , Jean-Louis Charliand Isabelle Florent
Abstract
Metallo-aminopeptidases (mAPs) control many physiological processes. They are classified in different families according to structural similarities. Neutral mAPs catalyze the cleavage of neutral amino acids from the N-terminus of proteins or peptide substrates; they need one or two metallic cofactors in their active site. Information about marine invertebrate’s neutral mAPs properties is scarce; available data are mainly derived from genomics and cDNA studies. The goal of this work was to characterize the biochemical properties of the neutral APs activities in eight Cuban marine invertebrate species from the Phyla Mollusca, Porifera, Echinodermata, and Cnidaria. Determination of substrate specificity, optimal pH and effects of inhibitors (1,10-phenanthroline, amastatin, and bestatin) and cobalt on activity led to the identification of distinct neutral AP-like activities, whose biochemical behaviors were similar to those of the M1 and M17 families of mAPs. Additionally, M18-like glutamyl AP activities were detected. Thus, marine invertebrates express biochemical activities likely belonging to various families of metallo-aminopeptidases.
Funding source: International Union of Biochemistry and Molecular Biology
Funding source: Agence Nationale de la Recherche
Award Identifier / Grant number: ANR-12-BS07-0020-02 project MAMMAMIA: “design of potential anti MAlarial M1/M17 AMinopeptiIdase Agents”
Acknowledgments
The authors thank the IUBMB Mid-Career fellowship program (research of IPA at IF and JLC laboratories) and the French ANR-12-BS07-0020-02 project MAMMAMIA “design of potential antiMAlarial M1/M17 AMinopeptiIdase Agents”, 2012–2017. We also thank Prof. Jose Espinosa, from the National Institute of Oceanology, CITMA, Cuba, who kindly provided species pictures included in Figure 1 and in Supplementary Material, Figure 2.
Author contribution: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: The authors thank the IUBMB Mid-Career fellowship program (research of IPA at IF and JLC laboratories) and the French ANR-12-BS07-0020-02 project MAMMAMIA “design of potential antiMAlarial M1/M17 AMinopeptiIdase Agents”, 2012–2017.
Employment or leadership: None declared.
Honorarium: None declared.
Conflict of interest statement: The authors declare no conflicts of interest regarding this article.
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Supplementary material
The online version of this article offers supplementary material (https://doi.org/10.1515/ZNC-2019-0169).
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