Literature DB >> 24557708

Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids.

Juliana A P Chaves1, Carolina Sanchez-López, Mariana P B Gomes, Tháyna Sisnande, Bruno Macedo, Vanessa End de Oliveira, Carolina A C Braga, Luciana P Rangel, Jerson L Silva, Liliana Quintanar, Yraima Cordeiro.   

Abstract

Conversion of prion protein (PrP) to an altered conformer, the scrapie PrP (PrP(Sc)), is a critical step in the development of transmissible spongiform encephalopathies. Both Cu(II) and nucleic acid molecules have been implicated in this conversion. Full-length PrP can bind up to six copper ions; four Cu(II) binding sites are located in the octarepeat domain (residues 60-91), and His-96 and His-111 coordinate two additional copper ions. Experimental evidence shows that PrP binds different molecules, resulting in diverse cellular signaling events. However, there is little information about the interaction of macromolecular ligands with Cu(II)-bound PrP. Both RNA and DNA sequences can bind PrP, and this interaction results in reciprocal conformational changes. Here, we investigated the interaction of Cu(II) and nucleic acids with amyloidogenic non-octarepeat PrP peptide models (comprising human PrP residues 106-126 and hamster PrP residues 109-149) that retain His-111 as the copper-anchoring residue. The effect of Cu(II) and DNA or RNA sequences in the aggregation, conformation, and toxicity of PrP domains was investigated at low and neutral pH. Circular dichroism and EPR spectroscopy data indicate that interaction of the PrP peptides with Cu(II) and DNA occurs at pH 7. This dual interaction induces conformational changes in the peptides, modulating their aggregation, and affecting the morphology of the aggregated species, resulting in different cytotoxic effects. These results provide new insights into the role of Cu(II) and nucleic acid sequences in the structural conversion and aggregation of PrP, which are both critical events related to prion pathogenesis.

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Year:  2014        PMID: 24557708     DOI: 10.1007/s00775-014-1115-8

Source DB:  PubMed          Journal:  J Biol Inorg Chem        ISSN: 0949-8257            Impact factor:   3.358


  54 in total

Review 1.  Prion protein and its conformational conversion: a structural perspective.

Authors:  Witold K Surewicz; Marcin I Apostol
Journal:  Top Curr Chem       Date:  2011

Review 2.  Intriguing nucleic-acid-binding features of mammalian prion protein.

Authors:  Jerson L Silva; Luís Maurício T R Lima; Debora Foguel; Yraima Cordeiro
Journal:  Trends Biochem Sci       Date:  2008-02-19       Impact factor: 13.807

Review 3.  The peculiar interaction between mammalian prion protein and RNA.

Authors:  Mariana P B Gomes; Yraima Cordeiro; Jerson L Silva
Journal:  Prion       Date:  2008-04-11       Impact factor: 3.931

4.  Diffusible, nonfibrillar ligands derived from Abeta1-42 are potent central nervous system neurotoxins.

Authors:  M P Lambert; A K Barlow; B A Chromy; C Edwards; R Freed; M Liosatos; T E Morgan; I Rozovsky; B Trommer; K L Viola; P Wals; C Zhang; C E Finch; G A Krafft; W L Klein
Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

5.  A mutational study in the transmembrane domain of Ccc2p, the yeast Cu(I)-ATPase, shows different roles for each Cys-Pro-Cys cysteine.

Authors:  Jennifer Lowe; Adalberto Vieyra; Patrice Catty; Florent Guillain; Elisabeth Mintz; Martine Cuillel
Journal:  J Biol Chem       Date:  2004-04-12       Impact factor: 5.157

6.  Neurotoxicity of a prion protein fragment.

Authors:  G Forloni; N Angeretti; R Chiesa; E Monzani; M Salmona; O Bugiani; F Tagliavini
Journal:  Nature       Date:  1993-04-08       Impact factor: 49.962

7.  Preferential Cu2+ coordination by His96 and His111 induces beta-sheet formation in the unstructured amyloidogenic region of the prion protein.

Authors:  Christopher E Jones; Salama R Abdelraheim; David R Brown; John H Viles
Journal:  J Biol Chem       Date:  2004-05-15       Impact factor: 5.157

Review 8.  Neurotoxic species in prion disease: a role for PrP isoforms?

Authors:  Christopher F Harrison; Kevin J Barnham; Andrew F Hill
Journal:  J Neurochem       Date:  2007-10-17       Impact factor: 5.372

9.  Scrapie-like prion protein is translocated to the nuclei of infected cells independently of proteasome inhibition and interacts with chromatin.

Authors:  Alain Mangé; Carole Crozet; Sylvain Lehmann; Florence Béranger
Journal:  J Cell Sci       Date:  2004-05-01       Impact factor: 5.285

10.  Prion protein complexed to N2a cellular RNAs through its N-terminal domain forms aggregates and is toxic to murine neuroblastoma cells.

Authors:  Mariana P B Gomes; Thiago A Millen; Priscila S Ferreira; Narcisa L Cunha e Silva; Tuane C R G Vieira; Marcius S Almeida; Jerson L Silva; Yraima Cordeiro
Journal:  J Biol Chem       Date:  2008-05-01       Impact factor: 5.157

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  3 in total

Review 1.  Using NMR spectroscopy to investigate the role played by copper in prion diseases.

Authors:  Rawiah A Alsiary; Mawadda Alghrably; Abdelhamid Saoudi; Suliman Al-Ghamdi; Lukasz Jaremko; Mariusz Jaremko; Abdul-Hamid Emwas
Journal:  Neurol Sci       Date:  2020-04-24       Impact factor: 3.307

2.  Mammalian prion protein (PrP) forms conformationally different amyloid intracellular aggregates in bacteria.

Authors:  Bruno Macedo; Ricardo Sant'Anna; Susanna Navarro; Yraima Cordeiro; Salvador Ventura
Journal:  Microb Cell Fact       Date:  2015-11-04       Impact factor: 5.328

Review 3.  Unraveling Prion Protein Interactions with Aptamers and Other PrP-Binding Nucleic Acids.

Authors:  Bruno Macedo; Yraima Cordeiro
Journal:  Int J Mol Sci       Date:  2017-05-17       Impact factor: 5.923

  3 in total

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