1,721,029 research outputs found

    Chaperones, chaperonins and heat-shock proteins

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    The protein folding of a nascent polypeptide is the decoding of the linear information contained in the primary sequence into the native and functionally active three-dimensional conformation. Chaperone proteins and folding catalysts may contribute to successful folding into the native and active protein conformation in the crowded cellular environment, thus avoiding aggregation of non-native protein forms. Molecular chaperones in vivo play a pivotal role in the maintenance of the proteome quality control and in the correct balance between protein folding and degradation. The unbalance of the equilibrium between protein synthesis, protein folding and protein degradation may contribute to protein misfolding and aggregation which may lead to the onset of several degenerative diseases associated with protein aggregation, such as Alzheimer’s and Huntington’s disease

    Fondamenti di biochimica umana

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    In quest’opera gli aspetti più importanti della biochimica umana sono stati raggruppati in tre temi unificanti: biomolecole funzionali e strutturali (vitamine, modulatori dello stress ossidativo, ormoni e lipidi bioattivi, neurotrasmettitori e componenti del citoscheletro); biochimica d’organo (cuore, fegato, apparato digerente, reni, sangue, apparato riproduttivo, apparato muscolare, osso, tessuto adiposo, cute e sistema nervoso); biochimica speciale (biochimica del tumore, fecondazione e sviluppo embrionale, metalli, stato redox e infiammazione, biochimica dei sensi, biochimica della nutrizione e biochimica clinica

    Proto-oncogene Pim-1: structural stability of the variants observed in tumor tissues

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    Pim-1 kinase belongs to the family of serine/threonine protein kinases (EC 2.7.11.1) encoded by the pim proto-oncogenes (Saris et al., 1991; Hoover et al., 1991; van der Lugt et al., 1995). Pim-1 kinase, originally identified as a common Proviral insertion site in moloney murine leukemia virus-induced T-cell lymphomas in mice (Cuypers et al., 1984), is involved in several signalling pathways and in the regulation of cell cycle progression and apoptosis. The three Pim family members Pim-1, Pim-2 and Pim-3 identified in humans have been reported as signalling protein kinases playing an important role in tumor biology (Anizon et al., 2010). Pim-1, nearly undetectable in normal tissues, is overexpressed in many haematological malignancies and in the cells of several solid tumor. In several cancer tissues Pim-1 variants have been identified and several databases for patterns of somatic mutation in human cancer genomes report mutations in this oncogene (Yuan et al., 2006; Greenman et al., 2007; Forbes et al., 2008; Akagi et al., 2009). Many of these variants are nonsynonymous single nucleotide polymorphisms (nsSNPs), single nucleotide variations occurring in the coding region and leading to amino acid substitutions (Dixit A et al., 2009). In this study we investigated the effect of amino acid substitution on the structural stability and on the activity of the Pim-1 kinase. We expressed and purified as soluble recombinant proteins some of the mutants identified in cancer and in the nsSNPs database. The mutants show a decreased thermal and thermodynamic stability and decreased activation energy relative to kinase activity, when compared to the wild- type

    Beta-Sheet-breaker peptides containing alfa, beta-dehydrophenylalanine: synthesis and in vitro activity studies

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    The synthesis and fibrillogenesis-inhibiting activity of the new peptide derivatives 1–6, containing α,β-unsaturated phenylalanines, are reported. These compounds are related to the pentapeptide Ac-LPFFD-NH2 (iAβ5p), which was designed by Soto and co-workers and is commonly accepted as a lead compound for fibrillogenesis inhibition . Their activities are determined by Thioflavin T binding assay, far-UV circular dichroism (CD) spectroscopy , and SEM; in addition, their structures in solution are studied through far-UV CD and FTIR spectroscopy. The presence of two α,β-unsaturated phenylalanines increases the fibrillogenesis inhibiting activity significantly in comparison with the lead compound. The interactions between the Aβ1–40 and the inhibitors using electrospray ionization mass spectrometry are also studied. The analyses prove the presence of noncovalent complexes of Aβ1–40 with iAβ5p and its derivatives 1–3 with stoichiometries of 1:1 and 2:1, and the results are independent of time and Aβ1–40/inhibitor rati

    The unusual co-assembly of H- and M-chains in the ferritin molecule from the Antarctic teleosts Trematomus bernacchii and Trematomus newnesi

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    Ferritins from the liver and spleen of the cold-adapted Antarctic teleosts Trematomus bernacchii and Trematomus newnesi have been isolated and characterized. Interestingly, only H- and M-chains are expressed and no L-chains. The H-chains contain the conserved ferroxidase center residues while M-chains harbor both the ferroxidase center and the micelle nucleation site ligands. Ferritins have an organ-specific subunit composition, they are: M homopolymers in spleen and H/M heteropolymers in liver. The M-chain homopolymer mineralizes iron at higher rate with respect to the H/M heteropolymer, which however is endowed with a lower activation energy for the iron incorporation process, indicative of a higher local flexibility. These findings and available literature data on ferritin expression in fish point to the role of tissue-specific expression of different chains in modulating the iron oxidation/mineralization process. © 2008 Elsevier Inc. All rights reserved
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