Jump to main content
Jump to site search

Volume 196, 2017
Previous Article Next Article

Deciphering the binding behaviours of BSA using ionic AIE-active fluorescent probes

Author affiliations


The binding behaviours of a transport protein, bovine serum albumin (BSA), in its native, unfolding and refolding states have been probed by monitoring the emission changes of two exogenous AIE-active fluorescent probes, M2 and M3, which are designed to be anionic and cationic, respectively. Due to their AIE properties, both M2 and M3 display emission enhancement when bound to the hydrophobic cavity of BSA. The binding site of M2 and M3 is found to be subdomain IIA. Then, the BSA + M2 and BSA + M3 systems are utilized to fluorescently signal the conformation changes of BSA caused by various external stimuli, including thermally or chemically induced denaturation. The data confirmed the multi-step unfolding process and the existence of a molten-globule intermediate state. The unfolding process consists of the rearrangement of subdomain IIA, the exposure of a negatively charged binding site in domain I that prefers interacting with cationic species, and the transformation of the molten-globule intermediate into the final random coil. The anionic and cationic modifications of the probes enable us to observe that electrostatic interactions play a role in the folding and unfolding of BSA.

Back to tab navigation

Supplementary files

Publication details

The article was received on 29 Jun 2016, accepted on 25 Jul 2016 and first published on 25 Jul 2016

Article type: Paper
DOI: 10.1039/C6FD00165C
Citation: Faraday Discuss., 2017,196, 285-303

  •   Request permissions

    Deciphering the binding behaviours of BSA using ionic AIE-active fluorescent probes

    J. Tong, T. Hu, A. Qin, J. Z. Sun and B. Z. Tang, Faraday Discuss., 2017, 196, 285
    DOI: 10.1039/C6FD00165C

Search articles by author