Characterization of the cytoplasmic chaperonin containing TCP-1 from the Antarctic fish Notothenia coriiceps.

• Published in: Extremophiles
• Main Authors: Pucciarelli, Sandra, Parker, Sandra K, Detrich, H William, Melki, Ronald
• Other Authors: School of biosciences and biotechnology, University of Camerino, Università degli Studi di Camerino = University of Camerino (UNICAM), National ecological observatory network, Department of Biology, Northeastern University, Northeastern University Boston, Laboratoire d'Enzymologie et Biochimie Structurales (LEBS), Centre National de la Recherche Scientifique (CNRS)
• Format: Article in Journal/Newspaper
• Language: English
• Published: HAL CCSD 2006
• Subjects: MESH: Adaptation; Physiological; MESH: Amino Acid Sequence; MESH: Male; MESH: Models; Molecular; MESH: Molecular Sequence Data; MESH: Perciformes; MESH: Protein Binding; MESH: Protein Conformation; MESH: Protein Denaturation; MESH: Protein Folding; MESH: Protein Subunits; MESH: Sequence Alignment; MESH: Animals; MESH: Sequence Analysis; Protein; MESH: Sequence Homology; Amino Acid; MESH: Testis; MESH: Tubulin; MESH: Antarctic Regions; MESH: Chaperonin Containing TCP-1; MESH: Chaperonins; MESH: Cold Climate; MESH: Cytoplasm; MESH: Cytoskeletal Proteins; MESH: Fish Proteins; [SDV]Life Sciences [q-bio]; Antarctic; Southern Ocean; The Antarctic; Antarc*
• Online Access: https://hal.archives-ouvertes.fr/hal-01183823; https://doi.org/10.1007/s00792-006-0528-x

International audience The cytoplasmic chaperonin containing TCP-1 (CCT) plays a critically important role in the folding and biogenesis of many cytoskeletal proteins, including tubulin and actin. For marine ectotherms, the chronically cold Southern Ocean (-2 to +2 degrees C) poses energetic challenges to protein folding, both at the level of substrate proteins and with respect to the chaperonin/chaperone folding system. Here we report the partial functional and structural characterization of CCT from an Antarctic notothenioid fish, Notothenia coriiceps. We find that the mechanism of folding by the Antarctic fish CCT differed from that of mammalian CCT: (1) the former complex was able to bind denatured beta-tubulin but (2) when reconstituted with rabbit Cofactor A, failed to release the protein to yield the tubulin/cofactor intermediate. Moreover, the amino acid sequences of the N. coriiceps CCT beta and theta chains contained residue substitutions in the equatorial, apical, and intermediate domains that would be expected to increase the flexibility of the subunits, thus facilitating function of the chaperonin in an energy poor environment. Our work contributes to the growing realization that protein function in cold-adapted organisms reflects a delicate balance between the necessity of structural flexibility for catalytic activity and the concomitant hazard of cold-induced denaturation.