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Mascolo, C.

Publications and source records attributed to Mascolo, C..

3 recordsLinked to original sources

New Swiss-knife activities of GroEL/Hsp60 proteins

GroEL/Hsp60 chaperonins are key proteins that control cell metabolism, stress adaptation and survival. They usually form a tetradecameric structure that assists, coupled to ATP hydrolysis, 10% of all cellular protein folding. Using recombinant E. coli, human mitochondrial and M. tuberculosis chaperonins, we found that these proteins have thioesterase, esterase and even, for some of them, auto-acyltransferase activities. The smaller oligomers of Hsp60 and M. tuberculosis GroEL1 were more prone to use the long acyl carbon chain substrate palmitoyl-CoA compared to tetradecameric E. coli GroEL and Hsp60. Enzymatic competition and replacement of M. tuberculosis GroEL1 residues allow identifying Asp86 and Thr89 in the ATP-binding pocket and an additional Ser393 influencing the thioesterase activity. Additionally, M. tuberculosis GroEL1 might enhance palmitoylation of the PpsE protein, which plays a role in the phthiocerol dimycocerosate (PDIM) biosynthesis. This could explain at least partly the involvement of GroEL1 in PDIM biosynthesis and antibiotic resistance.

biochemistry↗

Carotenoid-based immune response in sea cucumbers relies on newly identified coelomocytes -- the carotenocytes

Sea cucumbers (Holothuroidea, Echinodermata) are marine deuterostomes possessing a complex innate immune system composed of a wide diversity of immune cells--coelomocytes, making them compelling models for exploring the evolution of immunity. This study investigates the functional specialisation of coelomocytes within the two main echinoderm body fluids, namely the perivisceral fluid (PF) from the perivisceral cavity and the hydrovascular fluid (HF) from the hydrovascular-- ambulacral system. Given their specific distribution restricted to the HF, hemocyte-like cells (HELs) are particularly investigated. In echinoderms, hemocytes have been described as reddish cells containing haemoglobin and thus presenting a function in oxygen transport. Using an integrative approach combining cell morphological analyses, pigment profiling and multi-omics technologies, we demonstrate, in the sea cucumber Holothuria forskali, that HELs harbour exceptionally high concentrations of carotenoids, primarily canthaxanthin and astaxanthin--potent antioxidant molecules responsible for their pigmentation. Transcriptomics and proteomics analyses reveal that HELs express candidate genes involved in the carotenoid metabolism pathway as well as catalase, an antioxidant enzyme. Additionally, spectral flow cytometry assays reveal that HELs do not produce reactive oxygen species in contrast to most coelomocyte types, reinforcing the hypothesis of their antioxidant function. HELs also contribute to the formation of large red bodies (i.e., coelomocyte aggregates) and increase in concentration following lipopolysaccharide injections, indicating an active role in immune defence. Given these results, we hypothesise that these cells act after the culmination of the immune response, forming an antioxidant shell around the cellular aggregates to mitigate oxidative stress from reactive oxygen species (ROS) produced within the aggregate while encapsulating pathogens, thus protecting the host tissues. The discovery of carotenoid-carrying coelomocytes constitutes the first report of pigmented coelomocytes in sea cucumbers (except respiratory pigments), challenging the long-standing assumption that these cells contain haemoglobin. Therefore, we propose renaming hemocytes into carotenocytes, at least in this species. However, we think that this newly described coelomocyte type has been wrongly identified as haemoglobin-containing cells in many previous studies and could be present in many other holothuroid species. Our findings thus establish a new paradigm in the study of coelomocytes in echinoderms as well as the function of the hydrovascular system, unique to this phylum.

evolutionary biology↗

Abundance, diversity and evolution of tyrosinase enzymes involved in the adhesive systems of mussels and tubeworms

The blue mussel (Mytilus edulis) and the honeycomb tubeworm (Sabellaria alveolata) have evolved similar adhesive systems to cope with the hydrodynamic conditions of the intertidal environment where they live. Both organisms can establish a permanent adhesion through the secretion of adhesive proteins rich in DOPA (3,4-dihydroxyphenylalanine), a post-translationally modified amino acid playing essential roles in interfacial adhesion and bulk cohesion. DOPA is produced by the hydroxylation of tyrosine residues by tyrosinase enzymes, which can also in some cases oxidise it further into dopaquinone Compared to the detailed knowledge available on mussel and tubeworm adhesive proteins, little information exists about the tyrosinases involved in their adhesive systems. By combining different molecular analyses, a catalogue of tyrosinase candidates potentially involved in the adhesive systems of M. edulis and S. alveolata was identified. Some of these candidates were shown to be expressed in the adhesive glands by in situ hybridization, with a high gland-specificity in mussels but not in tubeworms. The diversity of tyrosinases highlighted in the two species suggests the coexistence of different functions (monophenol monooxygenase or catechol oxidase activity) or different substrate specificities. However, the exact role of the different enzymes needs to be further investigated. Phylogenetic analyses support the hypothesis of independent expansions and parallel evolution of tyrosinases involved in adhesive protein maturation in both lineages, supporting the convergent evolution of their DOPA-based adhesion.

evolutionary biology↗