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Quantification of amyloid fibrils using size exclusion chromatography coupled with online fluorescence and ultraviolet detection.
- Source :
-
Analytical biochemistry [Anal Biochem] 2015 Nov 01; Vol. 488, pp. 19-21. Date of Electronic Publication: 2015 Jul 31. - Publication Year :
- 2015
-
Abstract
- An amyloid fibrils investigation within biofilm samples requires distinguishing the amyloid β-sheet structure of these proteins and quantifying them. In this study, the property of amyloids to incorporate the fluorescent dye Thioflavin T has been exploited to propose a method of quantification. The experimental protocol includes the preparation of amyloids from commercial κ-casein (κCN) and their fractionation through size exclusion chromatography (SEC) to provide calibration curves from fluorescence and absorbance signals. Finally, a bacterial biofilm extract was injected into SEC, and the amyloid fibrils could be expressed as equivalent κCN, representing approximately 21% of the total proteins.<br /> (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Subjects :
- Algorithms
Amyloid chemistry
Animals
Bacillus chemistry
Bacillus physiology
Bacterial Proteins analysis
Bacterial Proteins chemistry
Bacterial Proteins isolation & purification
Benzothiazoles
Biofilms
Calibration
Caseins analysis
Caseins chemistry
Cattle
Chromatography, Gel
Fluorescent Dyes chemistry
France
Molecular Weight
Protein Aggregates
Solubility
Spectrometry, Fluorescence
Spectrophotometry, Ultraviolet
Thiazoles chemistry
Amyloid analysis
Models, Molecular
Protein Aggregation, Pathological diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0309
- Volume :
- 488
- Database :
- MEDLINE
- Journal :
- Analytical biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 26239215
- Full Text :
- https://doi.org/10.1016/j.ab.2015.07.014