Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1217005 | Journal of Chromatography B | 2008 | 5 Pages |
Abstract
In this study, a protein purified by fluorescein isothiocyanate (FITC)-affinity chromatography from human plasma was identified as albumin by MALDI-TOF-MS. Albumin was found to conjugate with FITC-labeled molecules through a copper-dependent reaction. The formation of this complex was confirmed by methods including a newly developed “charcoal-based fluorescence assay” (CFA), gel-filtration, affinity chromatography, and ultrafiltration. The binding was identified as disulfide bridge formation. This is the first to demonstrate that copper induces a covalent binding of FITC-labeled molecules with albumin. In addition, the developed CFA method facilitates the screening of small fluorescent dyes binding to macromolecules.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Yu-Wei Wu, Sung-Fang Chen, Charng-Bin Yang, Yu-Hui Tsai,