Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/25715
Title: | Unveiling the Interaction of Vanadium Compounds with Human Serum Albumin by Using 1H STD NMR and Computational Docking Studies | Authors: | Dias, David M. Rodrigues, João P. G. L. M. Domingues, Neuza S. Bonvin, Alexandre M. J. J. Castro, M. M. C. A. |
Keywords: | Proteins; Docking studies; Drug delivery; Vanadium; NMR spectroscopy | Issue Date: | 2013 | Publisher: | Wiley-VCH Verlag | Serial title, monograph or event: | European Journal of Inorganic Chemistry | Volume: | 2013 | Issue: | 26 | Abstract: | The binding of the VV oxidation products of two vanadium( IV) compounds, [VO(dmpp)2] and [VO(maltolato)2], which have shown promising anti-diabetic properties, to human serum albumin (HSA) in aqueous aerobic solution has been studied by 1H saturation transfer difference (STD) NMR spectroscopy and computational docking studies. Group epitope mapping and docking simulations indicate a preference of HSA binding to the 1:1 [VO2(dmpp)(OH)(H2O)]– and 1:2 [VO2(maltol)2]– vanadium(V) species. By using known HSA binders, competition NMR experiments revealed that both complexes preferentially bind to drug site I. Docking simulations carried out with HADDOCK together with restraints derived from the STD results led to three-dimensional models that are in agreement with the NMR spectroscopic data, providing useful information on molecular interaction modes. These results indicate that the combination of STD NMR and data-driven docking is a good tool for elucidating the interactions in protein–vanadium compounds and thus for clarifying the mechanism of drug delivery as vanadium compounds have shown potential therapeutic properties. | URI: | https://hdl.handle.net/10316/25715 | DOI: | 10.1002/ejic.201300419 | Rights: | openAccess |
Appears in Collections: | FCTUC Ciências da Vida - Artigos em Revistas Internacionais |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
4619_ftp(1).pdf | 818.36 kB | Adobe PDF | View/Open |
SCOPUSTM
Citations
20
checked on Apr 1, 2024
WEB OF SCIENCETM
Citations
5
20
checked on Apr 2, 2024
Page view(s)
310
checked on Apr 16, 2024
Download(s)
299
checked on Apr 16, 2024
Google ScholarTM
Check
Altmetric
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.