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Article

Osmolyte-Like Stabilizing Effects of Low GdnHCl Concentrations on d-Glucose/d-Galactose-Binding Protein

1
Institute of Cytology of the Russian Academy of Sciences, Laboratory of Structural Dynamics, Stability and Folding of Proteins, Tikhoretsky av. 4, 194064 St. Petersburg, Russia
2
Saint Petersburg State University, Universitetskaya nab. 7/9, 199034 St. Petersburg, Russia
3
CNR, Institute of Food Science, via Roma 64, 83100 Avellino, Italy
4
Department of Molecular Medicine and Byrd Alzheimer’s Research Institute, Morsani College of Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., Tampa, FL 33612, USA
5
Department of Biophysics, Peter the Great St. Petersburg Polytechnic University, Polytechnicheskaya av. 29, 195251 St. Petersburg, Russia
*
Authors to whom correspondence should be addressed.
Int. J. Mol. Sci. 2017, 18(9), 2008; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18092008
Received: 29 August 2017 / Revised: 14 September 2017 / Accepted: 16 September 2017 / Published: 19 September 2017
(This article belongs to the Section Molecular Biophysics)
The ability of d-glucose/d-galactose-binding protein (GGBP) to reversibly interact with its ligands, glucose and galactose, makes this protein an attractive candidate for sensing elements of glucose biosensors. This potential is largely responsible for attracting researchers to study the conformational properties of this protein. Previously, we showed that an increase in the fluorescence intensity of the fluorescent dye 6-bromoacetyl-2-dimetylaminonaphtalene (BADAN) is linked to the holo-form of the GGBP/H152C mutant in solutions containing sub-denaturing concentrations of guanidine hydrochloride (GdnHCl). It was hypothesized that low GdnHCl concentrations might lead to compaction of the protein, thereby facilitating ligand binding. In this work, we utilize BADAN fluorescence spectroscopy, intrinsic protein UV fluorescence spectroscopy, and isothermal titration calorimetry (ITC) to show that the sub-denaturing GdnHCl concentrations possess osmolyte-like stabilizing effects on the structural dynamics, conformational stability, and functional activity of GGBP/H152C and the wild type of this protein (wtGGBP). Our data are consistent with the model where low GdnHCl concentrations promote a shift in the dynamic distribution of the protein molecules toward a conformational ensemble enriched in molecules with a tighter structure and a more closed conformation. This promotes the increase in the configurational complementarity between the protein and glucose molecules that leads to the increase in glucose affinity in both GGBP/H152C and wtGGBP. View Full-Text
Keywords: d-glucose/d-galactose-binding protein; guanidine hydrochloride; osmolyte-like stabilizing effect; fluorescent label BADAN; protein conformers; protein function; conformational ensemble d-glucose/d-galactose-binding protein; guanidine hydrochloride; osmolyte-like stabilizing effect; fluorescent label BADAN; protein conformers; protein function; conformational ensemble
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MDPI and ACS Style

Fonin, A.V.; Golikova, A.D.; Zvereva, I.A.; D’Auria, S.; Staiano, M.; Uversky, V.N.; Kuznetsova, I.M.; Turoverov, K.K. Osmolyte-Like Stabilizing Effects of Low GdnHCl Concentrations on d-Glucose/d-Galactose-Binding Protein. Int. J. Mol. Sci. 2017, 18, 2008. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18092008

AMA Style

Fonin AV, Golikova AD, Zvereva IA, D’Auria S, Staiano M, Uversky VN, Kuznetsova IM, Turoverov KK. Osmolyte-Like Stabilizing Effects of Low GdnHCl Concentrations on d-Glucose/d-Galactose-Binding Protein. International Journal of Molecular Sciences. 2017; 18(9):2008. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18092008

Chicago/Turabian Style

Fonin, Alexander V., Alexandra D. Golikova, Irina A. Zvereva, Sabato D’Auria, Maria Staiano, Vladimir N. Uversky, Irina M. Kuznetsova, and Konstantin K. Turoverov 2017. "Osmolyte-Like Stabilizing Effects of Low GdnHCl Concentrations on d-Glucose/d-Galactose-Binding Protein" International Journal of Molecular Sciences 18, no. 9: 2008. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18092008

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