Literature DB >> 23458420

Thioflavin T and its photoirradiative derivatives: exploring their spectroscopic properties in the absence and presence of amyloid fibrils.

Jack C-C Hsu1, Eric H-L Chen, Robert C Snoeberger, Frederick Y Luh, T-S Lim, C-P Hsu, Rita P-Y Chen.   

Abstract

In this work, we found that, during storage or after UV irradiation, ThT is demethylated or oxidized, forming three derivatives. These three derivatives were purified by high performance liquid chromatography and characterized by mass and nuclear magnetic resonance spectroscopy and the spectroscopic properties of pure ThT and the derivatives carefully compared. Our results show that the emission peak at 450 nm results from oxidized ThT and not from the monomeric form of ThT, as previously proposed. The partial conversion of ThT into oxidized and demethylated derivatives has an effect on amyloid detection using ThT assay. Irradiated ThT has the same lag time as pure ThT in the amyloidogenesis of insulin, but the intensity of the emitted fluorescence is significantly decreased.

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Year:  2013        PMID: 23458420     DOI: 10.1021/jp309331u

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  1 in total

1.  Location of the cross-β structure in prion fibrils: A search by seeding and electron spin resonance spectroscopy.

Authors:  Brett K-Y Chu; Ruei-Fong Tsai; Chien-Lun Hung; Yun-Hsuan Kuo; Eric H-L Chen; Yun-Wei Chiang; Sunney I Chan; Rita P-Y Chen
Journal:  Protein Sci       Date:  2022-06       Impact factor: 6.993

  1 in total

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