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Exceptionally enhanced Raman optical activity (ROA) of amyloid fibrils and their prefibrillar states.
Kolodziejczyk, Aleksandra; Nafie, Laurence A; Wajda, Aleksandra; Kaczor, Agnieszka.
Afiliação
  • Kolodziejczyk A; Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, Krakow 30-387, Poland. aleksandra.wajda@uj.edu.pl.
  • Nafie LA; Doctoral School of Exact and Natural Sciences, Jagiellonian University, Lojasiewicza 11, Krakow 30-348, Poland.
  • Wajda A; Department of Chemistry, Syracuse University, Syracuse, New York 13244, USA.
  • Kaczor A; Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, Krakow 30-387, Poland. aleksandra.wajda@uj.edu.pl.
Chem Commun (Camb) ; 59(72): 10793-10796, 2023 Sep 07.
Article em En | MEDLINE | ID: mdl-37594150
Amyloid fibrils form remarkable, multi-layered chiral supramolecular architectures. The proximity of interacting oscillators in the chiral fibril supramolecules is responsible for the unusual sensitivity of vibrational circular dichroism (VCD) for fibril formation. Surprisingly, up to now, such characteristics have not been shown for ROA, although it displays the same vibrational markers of fibrils as VCD, including the amide I band. Here, we report an exceptionally large enhancement of the ROA signal detected for mature amyloid fibrils and their prefibrillar states. Remarkably, the same ROA signal has been obtained for fibrils of homologous lysozymes and the dissimilar protein, insulin, indicating a possible common enhanced ROA spectrum, analogous to that for VCD for all amyloid fibrils investigated to date. The ROA signal is observed at earlier stages of fibril formation than VCD and provides access to a considerably broader range of vibrations. Further studies are necessary to verify the applicability of ROA for the analysis of amyloid fibrils.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amidas / Amiloide Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amidas / Amiloide Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Polônia País de publicação: Reino Unido