Differential stability of the triple helix of (Pro-Pro-Gly)10 in H2O and D2O:: Thermodynamic and structural explanations

被引:7
作者
Gough, CA [1 ]
Bhatnagar, RS [1 ]
机构
[1] Univ Calif San Francisco, Lab Connect Tissue Biochem, San Francisco, CA 94143 USA
关键词
D O I
10.1080/07391102.1999.10508379
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
(Pro-Pro-Gly)(10) [(PPG(10))], a collagen-like polypeptide, forms a triple-helical, polyproline-II structure in aqueous solution at temperatures somewhat lower than physiological, with a melting temperature of 24.5 degrees C. In this article, we present circular dichroism spectra that demonstrate an increase of the melting temperature with the addition of increasing amounts of D2O to an H2O solution of (PPG)(10), with the melting temperature reaching 40 degrees C in pure D2O. A thermodynamic analysis of the data demonstrates that this result is due to an increasing enthalphy of unfolding in D2O vs. H2O. To provide a theoretical explanation for this result, we have used a model for hydration of (PPG)(10) that we developed previously, in which inter-chain water bridges are formed between sterically crowded waters and peptide bond carbonyls. Energy minimizations were performed upon this model using hydrogen bond parameters for water, and altered hydrogen bond parameters that reproduced the differences in carbonyl oxygen-water oxygen distances found in small-molecule crystal structures containing oxygen-oxygen hydrogen bonds between organic molecules and H2O or D2O. It was found that using hydrogen bond parameters that reproduced the distance typical of hydrogen bonds to D2O resulted in a significant lowering of the potential energy of hydrated (PPG)(10). This lowering of the energy involved energetic terms that were only indirectly related to the altered hydrogen bond parameters, and were therefore not artifactual; the intra-(PPG(10)) energy, plus the water-(PPG(10)) van der Waals energy (not including hydrogen bond interactions), were lowered enough to qualitatively account for the lower enthalpy of the triple-helical conformation, relative to the unfolded state, in D2O vs. H2O. This result indicates that the geometry of the carbonyl-D2O hydrogen bonds allows formation of good hydrogen bonds without making as much of an energetic sacrifice from other factors as in the case of hydration by H2O.
引用
收藏
页码:481 / 491
页数:11
相关论文
共 34 条
[1]  
ATKINS PW, 1986, PHYSICAL CHEM
[2]   HYDROPHOBIC INTERACTION IN LIGHT AND HEAVY-WATER [J].
BENNAIM, A ;
WILF, J ;
YAACOBI, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1973, 77 (01) :95-102
[3]   INTER-CHAIN PROLINE - PROLINE CONTACTS CONTRIBUTE TO THE STABILITY OF THE TRIPLE HELICAL CONFORMATION [J].
BHATNAGAR, RS ;
PATTABIRAMAN, N ;
SORENSEN, KR ;
LANGRIDGE, R ;
MACELROY, RD ;
RENUGOPALAKRISHNAN, V .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1988, 6 (02) :223-&
[4]   POLYNUCLEOTIDE MELTING IN HEAVY AND LIGHT WATER [J].
BLAKE, RD .
BIOCHEMISTRY, 1981, 20 (20) :5735-5743
[5]   NMR AND CD STUDIES OF TRIPLE-HELICAL PEPTIDES [J].
BRODSKY, B ;
LI, MH ;
LONG, CG ;
APIGO, J ;
BAUM, J .
BIOPOLYMERS, 1992, 32 (04) :447-451
[6]   EFFECT OF DEUTERIUM ON THE STRENGTH OF HYDROGEN BONDS [J].
CALVIN, M ;
HERMANS, J ;
SCHERAGA, HA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1959, 81 (19) :5048-5050
[7]   A 2ND GENERATION FORCE-FIELD FOR THE SIMULATION OF PROTEINS, NUCLEIC-ACIDS, AND ORGANIC-MOLECULES [J].
CORNELL, WD ;
CIEPLAK, P ;
BAYLY, CI ;
GOULD, IR ;
MERZ, KM ;
FERGUSON, DM ;
SPELLMEYER, DC ;
FOX, T ;
CALDWELL, JW ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (19) :5179-5197
[8]   HYDROPHOBIC BOND IN MICELLAR SYSTEMS . EFFECTS OF VARIOUS ADDITIVES ON STABILITY OF MICELLES OF SODIUM DODECYL SULFATE AND OF N-DODECYLTRIMETHYLAMMONIUM BROMIDE [J].
EMERSON, MF ;
HOLTZER, A .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (10) :3320-&
[9]   TRIPLE HELIX REVERSIBLE COIL CONVERSION OF COLLAGEN-LIKE POLYTRIPEPTIDES IN AQUEOUS AND NON-AQUEOUS SOLVENTS - COMPARISON OF THERMODYNAMIC PARAMETERS AND BINDING OF WATER TO (L-PRO-L-PRO-GLY)N AND (L-PRO-L-HYP-GLY)N [J].
ENGEL, J ;
CHEN, HT ;
PROCKOP, DJ ;
KLUMP, H .
BIOPOLYMERS, 1977, 16 (03) :601-622
[10]   Biochemistry - Versatile collagens in invertebrates [J].
Engel, J .
SCIENCE, 1997, 277 (5333) :1785-1786