Many higher organisms have adapted to environmental stresses such as extremes of temperature, dehydration, and salt solutions concentrations of urea and their adaptations has involved intracellular accumulations of small organic solutes called 'osmolytes.' Osmolytes stabilize proteins and other cell components against the extreme conditions and do so without significantly altering the biological activity of the macromolecule. The long-term goals of our research are two-fold: (I) to understand the mechanisms by which natural occurring osmolytes protein proteins under deleterious structural effects brought about by denaturing environmental stresses, and (II) to understand the mechanisms by which the osmolytes ensure appropriate functional activity of proteins in the face of these mechanisms by which the osmolytes ensure appropriate functional activity of proteins in the face of these stresses. The hypothesis that osmolyte-induced shifts in the native state ensemble are responsible for their appropriate effects on function will be investigated. Previously, we found that osmolytes interact unfavorably with the peptide backbone of proteins and this fundamental property of osmolytes is responsible for the stabilization of proteins against the denaturing environmental stresses. We will study in more detail the basic properties of the peptide backbone in solution, as well as osmolytes of kidney, and evaluate their contributions to the Free Energy of transfer of structured peptides/proteins from water to osmolyte solutions, Two experimental metrics were identified that quantifies the ability of osmolytes to force proteins to folder and contract or expand the denatured ensemble. These metrics will be developed and used to test factors believed to be important in osmolyte action of proteins, including macromolecular crowding. The marked effects protecting osmolytes have on protein folding kinetics will be explored and contrasted with effects commonly observed in the presence of the non-protecting osmolyte urea. Medically, the osmolytes have protective roles in human kidney and are of value in pharmaceutical formulations of protein drugs.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM049760-11
Application #
6725442
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Program Officer
Basavappa, Ravi
Project Start
1993-08-01
Project End
2006-03-31
Budget Start
2004-04-01
Budget End
2005-03-31
Support Year
11
Fiscal Year
2004
Total Cost
$281,238
Indirect Cost
Name
University of Texas Medical Br Galveston
Department
Biochemistry
Type
Schools of Medicine
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555
Tischer, Alexander; Machha, Venkata R; Rösgen, Jörg et al. (2018) ""Cooperative collapse"" of the denatured state revealed through Clausius-Clapeyron analysis of protein denaturation phase diagrams. Biopolymers 109:e23106
Rösgen, Jörg (2015) Synergy in protein-osmolyte mixtures. J Phys Chem B 119:150-7
Dutta, Amit K; Rösgen, Jörg; Rajarathnam, Krishna (2015) Using isothermal titration calorimetry to determine thermodynamic parameters of protein-glycosaminoglycan interactions. Methods Mol Biol 1229:315-24
Rajarathnam, Krishna; Rösgen, Jörg (2014) Isothermal titration calorimetry of membrane proteins - progress and challenges. Biochim Biophys Acta 1838:69-77
Jackson-Atogi, Ruby; Sinha, Prem Kumar; Rosgen, Jorg (2013) Distinctive solvation patterns make renal osmolytes diverse. Biophys J 105:2166-74
Rosgen, Jorg; Jackson-Atogi, Ruby (2012) Volume exclusion and H-bonding dominate the thermodynamics and solvation of trimethylamine-N-oxide in aqueous urea. J Am Chem Soc 134:3590-7
Holthauzen, Luis Marcelo F; Auton, Matthew; Sinev, Mikhail et al. (2011) Protein stability in the presence of cosolutes. Methods Enzymol 492:61-125
Auton, Matthew; Rosgen, Jorg; Sinev, Mikhail et al. (2011) Osmolyte effects on protein stability and solubility: a balancing act between backbone and side-chains. Biophys Chem 159:90-9
Kokubo, Hironori; Hu, Char Y; Pettitt, B Montgomery (2011) Peptide conformational preferences in osmolyte solutions: transfer free energies of decaalanine. J Am Chem Soc 133:1849-58
Street, Timothy O; Krukenberg, Kristin A; Rosgen, Jorg et al. (2010) Osmolyte-induced conformational changes in the Hsp90 molecular chaperone. Protein Sci 19:57-65

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