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Conformation Control of Amyloid Filaments by Repeated Thermal Perturbation.
Lee, Sang Won; Choi, Hyunsung; Lee, Gyudo; Choi, Yeseong; Lee, Hyungbeen; Kim, Geehyuk; Lee, Hyeyoung; Lee, Wonseok; Park, Jinsung; Yoon, Dae Sung.
Afiliação
  • Lee SW; School of Biomedical Engineering, Korea University, Seoul 02841, South Korea.
  • Choi H; Center for Molecular Spectroscopy and Dynamics, Institute for Basic Science (IBS), Seoul 02841, South Korea.
  • Lee G; Department of Biotechnology and Bioinformatics, Korea University, Sejong 30019, South Korea.
  • Choi Y; Interdisciplinary Graduate Program for Artificial Intelligence Smart Convergence Technology, Korea University, Sejong 30019, South Korea.
  • Lee H; School of Biomedical Engineering, Korea University, Seoul 02841, South Korea.
  • Kim G; Department of Pharmacology, College of Pharmacy, Kyung Hee University, Seoul 02447, South Korea.
  • Lee H; R&D Center of Curigin Ltd., Seoul 04778, Republic of Korea.
  • Lee W; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, South Korea.
  • Park J; Department of Biomedical Laboratory Science, Yonsei University, Wonju 26493, South Korea.
  • Yoon DS; Department of Electrical Engineering, Korea National University of Transportation, Chungju 27469, South Korea.
ACS Macro Lett ; 10(12): 1549-1554, 2021 12 21.
Article em En | MEDLINE | ID: mdl-35549127
ABSTRACT
We report that repeated thermal perturbation by thermal cycling (TC) accelerates the formation rate of amyloid filaments at microliter volumes (10-200 µL) and produces a new conformation of zigzag-shaped filaments. The amyloid filaments have been synthesized under different TC conditions, such as temperature variations (ΔT = 0-86 °C) and the number of cycles (C# = 30-90). In particular, the filament formation was promoted by TC with ΔT ≥ 30 °C. This indicates that the change in binding energy of ß-sheets and the breakage of disulfide bonds induced by TC with large ΔT contributed to the increased filament growth. This molecular interaction was investigated by molecular dynamics simulation. We also found that TC leads to the formation of amyloid filaments with peculiar conformation (zigzag-shaped filaments). Moreover, key structural parameters (tortuosity, segment length, and joint angle) of the amyloid filaments could be fine-tuned by selecting certain ΔT conditions. Taken together, we confirmed that the TC not only promotes the formation of amyloid filaments but also affects the conformational changes of the filaments.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amiloide / Amiloidose Limite: Humans Idioma: En Revista: ACS Macro Lett Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Amiloide / Amiloidose Limite: Humans Idioma: En Revista: ACS Macro Lett Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Coréia do Sul