Albumin-induced circular dichroism in Congo red: applications for studies of amyloid-like fibril aggregates and binding sites
| dc.contributor.author | Vasconcelos, Débora Naliati de [UNESP] | |
| dc.contributor.author | Ximenes, Valdecir Farias [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
| dc.date.accessioned | 2015-12-07T15:40:36Z | |
| dc.date.available | 2015-12-07T15:40:36Z | |
| dc.date.issued | 2015-11-05 | |
| dc.description.abstract | Congo red (CR), one of the most commonly used dyes for the identification of amyloid fibril aggregates, is also a ligand of native bovine serum albumin (BSA). Induced circular dichroism (ICD) is a phenomenon observed when a chiral compound induces chirality in an achiral one. Here, we study the spectral properties and analytical applications of ICD in Congo red provoked by its interaction with BSA. The complex BSA:CR displays a strong ICD spectrum with a positive band at 412nm and two negative bands at 356 and 490nm. The use of site I and site II albumin ligands as warfarin and ibuprofen, respectively, provoked different alterations in the Congo red ICD spectrum. The BSA binding sites were modified by oxidation and the ICD signal was sensitive to this alteration. The thermal treatment of the BSA:CR complex (30-90°C) was monitored by ICD at 490nm and showed a sigmoidal pattern typical of phase transition in proteins. The altered ICD spectrum is consistent with the formation of amyloid-like fibril aggregates in BSA, which was confirmed by thioflavin T and Rayleigh scattering assays. In conclusion, the ICD provoked by the binding of Congo red to albumin may represent a new spectroscopic technique for studying alterations in the structure of albumin regarding its binding sites and the formation of amyloid aggregates. | en |
| dc.description.affiliationUnesp | Universidade Estadual Paulista, Departamento de Química, Faculdade de Ciências de Bauru | |
| dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
| dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
| dc.description.sponsorshipId | FAPESP: 2013/08784-0 | |
| dc.format.extent | 321-330 | |
| dc.identifier | http://dx.doi.org/10.1016/j.saa.2015.05.089 | |
| dc.identifier.citation | Spectrochimica Acta. Part A, Molecular And Biomolecular Spectroscopy, v. 150, p. 321-330, 2015. | |
| dc.identifier.doi | 10.1016/j.saa.2015.05.089 | |
| dc.identifier.issn | 1873-3557 | |
| dc.identifier.lattes | 4066413997908572 | |
| dc.identifier.pubmed | 26056983 | |
| dc.identifier.uri | http://hdl.handle.net/11449/131688 | |
| dc.language.iso | eng | |
| dc.publisher | Elsevier B. V. | |
| dc.relation.ispartof | Spectrochimica Acta. Part A, Molecular And Biomolecular Spectroscopy | |
| dc.rights.accessRights | Acesso restrito | |
| dc.source | PubMed | |
| dc.subject | Albumin | en |
| dc.subject | Amyloid aggregates | en |
| dc.subject | Binding sites | en |
| dc.subject | Congo red | en |
| dc.subject | Induced circular dichroism | en |
| dc.title | Albumin-induced circular dichroism in Congo red: applications for studies of amyloid-like fibril aggregates and binding sites | en |
| dc.type | Artigo | |
| dcterms.rightsHolder | Elsevier B. V. | |
| unesp.author.lattes | 4066413997908572 | |
| unesp.campus | Universidade Estadual Paulista (Unesp), Faculdade de Ciências, Bauru | pt |