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Volumn , Issue , 2013, Pages 169-210

The importance of water

(1)  Ball, Philip a  

a NONE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROPHOBICITY; SUBSTRATES;

EID: 84969821158     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-642-31730-9_6     Document Type: Chapter
Times cited : (15)

References (118)
  • 2
    • 0346095503 scopus 로고    scopus 로고
    • Microbes made to order
    • Ferber D (2004) Microbes made to order. Science 303: 158-161
    • (2004) Science , vol.303 , pp. 158-161
    • Ferber, D.1
  • 4
    • 0036851660 scopus 로고    scopus 로고
    • Replacing the nucleobases in DNA with designer molecules
    • Kool ET (2002) Replacing the nucleobases in DNA with designer molecules. Acc Chem Res 35: 936-943
    • (2002) Acc Chem Res , vol.35 , pp. 936-943
    • Kool, E.T.1
  • 5
    • 38849196324 scopus 로고    scopus 로고
    • Water as an active constituent in cell biology
    • Ball P (2007) Water as an active constituent in cell biology. Chem Rev 108: 74-108
    • (2007) Chem Rev , vol.108 , pp. 74-108
    • Ball, P.1
  • 6
    • 0014012048 scopus 로고
    • Deuterated organisms: Cultivation and uses
    • Katz JJ, Crespi HL (1966) Deuterated organisms: cultivation and uses. Science 151: 1187-1194
    • (1966) Science , vol.151 , pp. 1187-1194
    • Katz, J.J.1    Crespi, H.L.2
  • 7
    • 9144227159 scopus 로고    scopus 로고
    • Is there a common chemical model for life in the universe?
    • Benner SA, Ricardo A, Carrigan MA (2004) Is there a common chemical model for life in the universe? Curr Opin Chem Biol 8: 672-689
    • (2004) Curr Opin Chem Biol , vol.8 , pp. 672-689
    • Benner, S.A.1    Ricardo, A.2    Carrigan, M.A.3
  • 8
    • 0041821388 scopus 로고    scopus 로고
    • Dehydron: A structurally encoded signal for protein interaction
    • Fernández A, Scott R (2003) Dehydron: a structurally encoded signal for protein interaction. Biophys J 85: 1914-1928
    • (2003) Biophys J , vol.85 , pp. 1914-1928
    • Fernández, A.1    Scott, R.2
  • 10
  • 12
    • 33744501242 scopus 로고    scopus 로고
    • Tetrahedral structure or chains for liquid water
    • Head-Gordon T, Johnson ME (2006) Tetrahedral structure or chains for liquid water. Proc Natl Acad Sci USA 103: 7973-7977
    • (2006) Proc Natl Acad Sci USA , vol.103 , pp. 7973-7977
    • Head-Gordon, T.1    Johnson, M.E.2
  • 13
    • 0002300553 scopus 로고    scopus 로고
    • Hydrogen-bond kinetics in liquid water
    • Luzar A, Chandler D (1996) Hydrogen-bond kinetics in liquid water. Nature 379: 55-57
    • (1996) Nature , vol.379 , pp. 55-57
    • Luzar, A.1    Chandler, D.2
  • 14
    • 0009502708 scopus 로고
    • Effects of defects on molecular mobility in liquid water
    • Sciortino F, Geiger A, Stanley HE (1991) Effects of defects on molecular mobility in liquid water. Nature 354: 218-221
    • (1991) Nature , vol.354 , pp. 218-221
    • Sciortino, F.1    Geiger, A.2    Stanley, H.E.3
  • 15
  • 19
    • 83455162896 scopus 로고    scopus 로고
    • Water-exclusion and liquid-structure forces in implicit solvation
    • Hassan S, Steinbach P (2011) Water-exclusion and liquid-structure forces in implicit solvation. J Phys Chem B 115: 14668-14682
    • (2011) J Phys Chem B , vol.115 , pp. 14668-14682
    • Hassan, S.1    Steinbach, P.2
  • 23
    • 33750286994 scopus 로고    scopus 로고
    • Do we underestimate the importance of water in cell biology?
    • ChaplinM(2006) Do we underestimate the importance of water in cell biology? Nat Rev Mol Cell Biol 7: 861-866
    • (2006) Nat Rev Mol Cell Biol , vol.7 , pp. 861-866
    • Chaplin, M.1
  • 24
    • 44049105071 scopus 로고    scopus 로고
    • Cell water dynamics on multiple time scales
    • Halle B, Persson E (2008) Cell water dynamics on multiple time scales. Proc Natl Acad Sci USA 105: 6266-6271
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 6266-6271
    • Halle, B.1    Persson, E.2
  • 26
  • 27
    • 36849117971 scopus 로고
    • Free volume and entropy in condensed systems. III. Entropy in binary liquid mixtures; partial molal entropy in dilute solutions; structure and thermodynamics in aqueous solutions
    • Frank HS, Evans MW (1945) Free volume and entropy in condensed systems. III. Entropy in binary liquid mixtures; partial molal entropy in dilute solutions; structure and thermodynamics in aqueous solutions. J Chem Phys 13: 507-532
    • (1945) J Chem Phys , vol.13 , pp. 507-532
    • Frank, H.S.1    Evans, M.W.2
  • 28
    • 0008863560 scopus 로고
    • Some factors in the interpretation of protein denaturation
    • Kauzmann W (1969) Some factors in the interpretation of protein denaturation. Adv Protein Chem 14: 1-63
    • (1969) Adv Protein Chem , vol.14 , pp. 1-63
    • Kauzmann, W.1
  • 29
    • 0038446327 scopus 로고    scopus 로고
    • How to keep dry in water
    • Ball P (2003) How to keep dry in water. Nature 423: 25-26
    • (2003) Nature , vol.423 , pp. 25-26
    • Ball, P.1
  • 30
    • 0011960339 scopus 로고    scopus 로고
    • Hydrophobicity at small and large length scales
    • Lum K, Chandler D, Weeks JD (1999) Hydrophobicity at small and large length scales. J Phys Chem B 103: 4570-4577
    • (1999) J Phys Chem B , vol.103 , pp. 4570-4577
    • Lum, K.1    Chandler, D.2    Weeks, J.D.3
  • 31
    • 33751155475 scopus 로고
    • Computer simulation of hydrophobic hydration forces on stacked plates at short range
    • Wallqvist A, Berne BJ (1995) Computer simulation of hydrophobic hydration forces on stacked plates at short range. J Phys Chem 99: 2893-2899
    • (1995) J Phys Chem , vol.99 , pp. 2893-2899
    • Wallqvist, A.1    Berne, B.J.2
  • 32
    • 0037076337 scopus 로고    scopus 로고
    • Drying-induced hydrophobic polymer collapse
    • ten Wolde PR, Chandler D (2002) Drying-induced hydrophobic polymer collapse. Proc Natl Acad Sci USA 99: 6539-6543
    • (2002) Proc Natl Acad Sci USA , vol.99 , pp. 6539-6543
    • ten Wolde, P.R.1    Chandler, D.2
  • 33
    • 80053634226 scopus 로고    scopus 로고
    • Signature of hydrophobic hydration in a single polymer
    • Li ITS, Walker GC (2011) Signature of hydrophobic hydration in a single polymer. Proc Natl Acad Sci USA 108: 16527-16532
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 16527-16532
    • Li, I.T.S.1    Walker, G.C.2
  • 34
    • 24344448662 scopus 로고    scopus 로고
    • Observation of a dewetting transition in the collapse of the melittin tetramer
    • Liu P, Huang X, Zhou R, Berne BJ (2005) Observation of a dewetting transition in the collapse of the melittin tetramer. Nature 437: 159-162
    • (2005) Nature , vol.437 , pp. 159-162
    • Liu, P.1    Huang, X.2    Zhou, R.3    Berne, B.J.4
  • 35
    • 4644236471 scopus 로고    scopus 로고
    • Hydrophobic collapse in multidomain protein folding
    • Zhou R, Huang X, Margulis CJ, Berne BJ (2004) Hydrophobic collapse in multidomain protein folding. Science 305: 1605-1609
    • (2004) Science , vol.305 , pp. 1605-1609
    • Zhou, R.1    Huang, X.2    Margulis, C.J.3    Berne, B.J.4
  • 36
    • 34548209898 scopus 로고    scopus 로고
    • Nanoscale dewetting transition in protein complex folding
    • Hua L, Huang X, Liu P, Zhou R, Berne BJ (2007) Nanoscale dewetting transition in protein complex folding. J Phys Chem B 111: 9069-9077
    • (2007) J Phys Chem B , vol.111 , pp. 9069-9077
    • Hua, L.1    Huang, X.2    Liu, P.3    Zhou, R.4    Berne, B.J.5
  • 38
    • 75749108542 scopus 로고    scopus 로고
    • Fluctuations of water near extended hydrophobic and hydrophilic surfaces
    • Patel AJ, Varrily P, Chandler D (2010) Fluctuations of water near extended hydrophobic and hydrophilic surfaces. J Phys Chem B 114: 1632-1637
    • (2010) J Phys Chem B , vol.114 , pp. 1632-1637
    • Patel, A.J.1    Varrily, P.2    Chandler, D.3
  • 39
    • 84857761874 scopus 로고    scopus 로고
    • Sitting at the edge: How biomolecules use hydrophobicity to tune their interactions and function
    • Patel AJ, Varilly P, Jamadagni SN, Hagan MF, Chander D, Garde S (2012) Sitting at the edge: how biomolecules use hydrophobicity to tune their interactions and function. J Phys Chem B. doi: 10.1021/jp2107523
    • (2012) J Phys Chem B.
    • Patel, A.J.1    Varilly, P.2    Jamadagni, S.N.3    Hagan, M.F.4    Chander, D.5    Garde, S.6
  • 41
    • 0347357617 scopus 로고    scopus 로고
    • Protein folding and misfolding
    • Dobson CM (2003) Protein folding and misfolding. Nature 426: 884-890
    • (2003) Nature , vol.426 , pp. 884-890
    • Dobson, C.M.1
  • 42
    • 33646161965 scopus 로고    scopus 로고
    • Role of topology, nonadditivity, and water-mediated interactions in predicting the structures of a/b proteins
    • Zong C, Papaoian GA, Ulander J, Wolynes PG (2006) Role of topology, nonadditivity, and water-mediated interactions in predicting the structures of a/b proteins. J Am Chem Soc 128: 5168-5176
    • (2006) J Am Chem Soc , vol.128 , pp. 5168-5176
    • Zong, C.1    Papaoian, G.A.2    Ulander, J.3    Wolynes, P.G.4
  • 44
    • 61749085446 scopus 로고    scopus 로고
    • Protein cold denaturation as seen from the solvent
    • Davidovic M, Mattea C, Qvist J, Halle B (2009) Protein cold denaturation as seen from the solvent. J Am Chem Soc 131: 1025-1036
    • (2009) J Am Chem Soc , vol.131 , pp. 1025-1036
    • Davidovic, M.1    Mattea, C.2    Qvist, J.3    Halle, B.4
  • 45
    • 55949131241 scopus 로고    scopus 로고
    • Urea denaturation by stronger dispersion interactions with proteins that water implies a 2-stage unfolding
    • Hua L, Zhou R, Thirumalai D, Berne BJ (2008) Urea denaturation by stronger dispersion interactions with proteins that water implies a 2-stage unfolding. Proc Natl Acad Sci USA 105: 16928-16933
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 16928-16933
    • Hua, L.1    Zhou, R.2    Thirumalai, D.3    Berne, B.J.4
  • 46
    • 51749109783 scopus 로고    scopus 로고
    • Chemical denaturants inhibit the onset of dewetting
    • England JL, Pande VS, Haran G (2008) Chemical denaturants inhibit the onset of dewetting. J Am Chem Soc 130: 11854-11855
    • (2008) J Am Chem Soc , vol.130 , pp. 11854-11855
    • England, J.L.1    Pande, V.S.2    Haran, G.3
  • 47
    • 63149153986 scopus 로고    scopus 로고
    • Urea’s action on hydrophobic interactions
    • Zangi R, Zhou R, Berne BJ (2009) Urea’s action on hydrophobic interactions. J Am Chem Soc 131: 1535-1541
    • (2009) J Am Chem Soc , vol.131 , pp. 1535-1541
    • Zangi, R.1    Zhou, R.2    Berne, B.J.3
  • 48
    • 0038370011 scopus 로고    scopus 로고
    • The molecular basis for the chemical denaturation of proteins by urea
    • Bennion BJ, Daggett V (2003) The molecular basis for the chemical denaturation of proteins by urea. Proc Natl Acad Sci USA 100: 5142-5147
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 5142-5147
    • Bennion, B.J.1    Daggett, V.2
  • 49
    • 79959343218 scopus 로고    scopus 로고
    • Preference for isolated water molecules in a concentrated glycerol-water mixture
    • Towey JJ, Soper AK, Dougan L (2011) Preference for isolated water molecules in a concentrated glycerol-water mixture. J Phys Chem B 115: 7799-7807
    • (2011) J Phys Chem B , vol.115 , pp. 7799-7807
    • Towey, J.J.1    Soper, A.K.2    Dougan, L.3
  • 50
    • 67649515630 scopus 로고    scopus 로고
    • The impact of polyols on water structure in solution: A computational study
    • Pioliti R, Sapir L, Harries D (2009) The impact of polyols on water structure in solution: a computational study. J Phys Chem A 113: 7548-7555
    • (2009) J Phys Chem A , vol.113 , pp. 7548-7555
    • Pioliti, R.1    Sapir, L.2    Harries, D.3
  • 51
    • 79959964603 scopus 로고    scopus 로고
    • Probing osmolyte participation in the unfolding transition state of a protein
    • Dougan L, Genchev GZ, Lu H, Fernández JM (2011) Probing osmolyte participation in the unfolding transition state of a protein. Proc Natl Acad Sci USA 108: 9759-9764
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 9759-9764
    • Dougan, L.1    Genchev, G.Z.2    Lu, H.3    Fernández, J.M.4
  • 52
    • 78650750083 scopus 로고    scopus 로고
    • Dry amyloid fibril assembly in a yeast prion peptide is mediated by long-lived structures containing water wires
    • Reddy G, Straub E, Thirumalai D (2010) Dry amyloid fibril assembly in a yeast prion peptide is mediated by long-lived structures containing water wires. Proc Natl Acad Sci USA 107: 21459-21464
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 21459-21464
    • Reddy, G.1    Straub, E.2    Thirumalai, D.3
  • 54
    • 79959543603 scopus 로고    scopus 로고
    • Non-adaptive origins of interactome complexity
    • Fernández A, Lynch M (2011) Non-adaptive origins of interactome complexity. Nature 474: 502-505
    • (2011) Nature , vol.474 , pp. 502-505
    • Fernández, A.1    Lynch, M.2
  • 56
    • 77956305291 scopus 로고    scopus 로고
    • Free energy, entropy, and enthalpy of a water molecule in various protein environments
    • Yu H, Rick S (2010) Free energy, entropy, and enthalpy of a water molecule in various protein environments. J Phys Chem B 114: 11552-11560
    • (2010) J Phys Chem B , vol.114 , pp. 11552-11560
    • Yu, H.1    Rick, S.2
  • 57
    • 77956075440 scopus 로고    scopus 로고
    • Water in cavity-ligand recognition
    • Baron R, Setny P, McCammon JA (2010) Water in cavity-ligand recognition. J Am Chem Soc 132: 12091-12097
    • (2010) J Am Chem Soc , vol.132 , pp. 12091-12097
    • Baron, R.1    Setny, P.2    McCammon, J.A.3
  • 59
    • 34250845103 scopus 로고    scopus 로고
    • Metastable water clusters in the nonpolar cavities of the thermostable protein tetrabrachion
    • Yin H, Hummer G, Rasaiah JC (2007) Metastable water clusters in the nonpolar cavities of the thermostable protein tetrabrachion. J Am Chem Soc 129: 7369-7377
    • (2007) J Am Chem Soc , vol.129 , pp. 7369-7377
    • Yin, H.1    Hummer, G.2    Rasaiah, J.C.3
  • 60
    • 79953251130 scopus 로고    scopus 로고
    • Adhesive water networks facilitate binding of protein interfaces
    • Ahmad M, Gu W, Geyer T, Helms V (2011) Adhesive water networks facilitate binding of protein interfaces. Nat Commun 2: 261
    • (2011) Nat Commun , vol.2 , pp. 261
    • Ahmad, M.1    Gu, W.2    Geyer, T.3    Helms, V.4
  • 61
    • 84961983691 scopus 로고    scopus 로고
    • Quantifying water-mediated protein-ligand interactions in a glutamate receptor: A DFT study
    • Sahai MA, Biggin PC (2011) Quantifying water-mediated protein-ligand interactions in a glutamate receptor: a DFT study. J Phys Chem B 115: 7085-7096
    • (2011) J Phys Chem B , vol.115 , pp. 7085-7096
    • Sahai, M.A.1    Biggin, P.C.2
  • 62
    • 0030471364 scopus 로고    scopus 로고
    • The role of water in sequenceindependent ligand binding by an oligopeptide transporter protein
    • Tame JRH, Sleigh SH, Wilkinson AJ, Ladbury JE (1996) The role of water in sequenceindependent ligand binding by an oligopeptide transporter protein. Nat Struct Biol 3: 998-1001
    • (1996) Nat Struct Biol , vol.3 , pp. 998-1001
    • Tame, J.R.H.1    Sleigh, S.H.2    Wilkinson, A.J.3    Ladbury, J.E.4
  • 64
    • 78650331566 scopus 로고    scopus 로고
    • Dynamics of water clusters confined in proteins: A molecular dynamics simulation study of interfacial waters in a dimeric hemoglobin
    • Gnanasekaran R, Xu Y, Leitner DM (2010) Dynamics of water clusters confined in proteins: a molecular dynamics simulation study of interfacial waters in a dimeric hemoglobin. J Phys Chem B 114: 16989-16996
    • (2010) J Phys Chem B , vol.114 , pp. 16989-16996
    • Gnanasekaran, R.1    Xu, Y.2    Leitner, D.M.3
  • 65
    • 34748815139 scopus 로고    scopus 로고
    • The hydrogen-bonding network in heme oxygenase also functions as a modulator of enzyme dynamics: Chaotic motions upon disrupting the H-bond network in heme oxygenase from Psuedomonas aeruginosa
    • Rodriquez JC, Zeng Y, Wilks A, Rivera M (2007) The hydrogen-bonding network in heme oxygenase also functions as a modulator of enzyme dynamics: chaotic motions upon disrupting the H-bond network in heme oxygenase from Psuedomonas aeruginosa. J Am Chem Soc 129: 11730-11742
    • (2007) J Am Chem Soc , vol.129 , pp. 11730-11742
    • Rodriquez, J.C.1    Zeng, Y.2    Wilks, A.3    Rivera, M.4
  • 66
    • 0035940261 scopus 로고    scopus 로고
    • Structure of the first-shell active site in metallolactamase: Effect of water ligands
    • Krauss M, Gilson HSR, Gresh N (2001) Structure of the first-shell active site in metallolactamase: effect of water ligands. J Phys Chem B 105: 8040-8049
    • (2001) J Phys Chem B , vol.105 , pp. 8040-8049
    • Krauss, M.1    Gilson, H.S.R.2    Gresh, N.3
  • 67
    • 34247549227 scopus 로고    scopus 로고
    • A water-mediated and substrate-assisted catalytic mechanism for Sulfolobus solfataricus DNA polymerase IV
    • Wang L, Yu X, Hu P, Broyde S, Zhang Y (2007) A water-mediated and substrate-assisted catalytic mechanism for Sulfolobus solfataricus DNA polymerase IV. J Am Chem Soc 129: 4731-4737
    • (2007) J Am Chem Soc , vol.129 , pp. 4731-4737
    • Wang, L.1    Yu, X.2    Hu, P.3    Broyde, S.4    Zhang, Y.5
  • 68
    • 44949182706 scopus 로고    scopus 로고
    • On the functional role of a water molecule in clade 3 catalases: A proposal for the mechanism by which NADPH prevents the formation of compound II
    • Sicking W, Korth H-G, de Groot H, Sustmann R (2008) On the functional role of a water molecule in clade 3 catalases: a proposal for the mechanism by which NADPH prevents the formation of compound II. J Am Chem Soc 130: 7345-7356
    • (2008) J Am Chem Soc , vol.130 , pp. 7345-7356
    • Sicking, W.1    Korth, H.-G.2    de Groot, H.3    Sustmann, R.4
  • 69
    • 11744384413 scopus 로고
    • The Grotthuss mechanism
    • Agmon N (1995) The Grotthuss mechanism. Chem Phys Lett 244: 456-462
    • (1995) Chem Phys Lett , vol.244 , pp. 456-462
    • Agmon, N.1
  • 70
    • 30144445932 scopus 로고    scopus 로고
    • Functional waters in intraprotein proton transfer monitored by FTIR Spectroscopy
    • Garczarek F, Gerwert K (2006) Functional waters in intraprotein proton transfer monitored by FTIR Spectroscopy. Nature 439: 109-112
    • (2006) Nature , vol.439 , pp. 109-112
    • Garczarek, F.1    Gerwert, K.2
  • 71
    • 34249857084 scopus 로고    scopus 로고
    • Structures and spectral signatures of protonated water networks in bacteriorhodopsin
    • Mathias G, Marx D (2007) Structures and spectral signatures of protonated water networks in bacteriorhodopsin. Proc Natl Acad Sci USA 104: 6980-6985
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 6980-6985
    • Mathias, G.1    Marx, D.2
  • 72
    • 33846021582 scopus 로고    scopus 로고
    • Charge delocalization in proton channels, I: The aquaporin channels and proton blockage
    • Chen H, Ilan B, Wu Y, Zhu F, Schulten K, Voth GA (2007) Charge delocalization in proton channels, I: the aquaporin channels and proton blockage. Biophys J 92: 46-60
    • (2007) Biophys J , vol.92 , pp. 46-60
    • Chen, H.1    Ilan, B.2    Wu, Y.3    Zhu, F.4    Schulten, K.5    Voth, G.A.6
  • 73
    • 33845936297 scopus 로고    scopus 로고
    • Localized proton microcircuits at the biological membrane-water interface
    • Brändén M, Sandén T, Brzezinski P, Widengren J (2006) Localized proton microcircuits at the biological membrane-water interface. Proc Natl Acad Sci USA 103: 19766-19770
    • (2006) Proc Natl Acad Sci USA , vol.103 , pp. 19766-19770
    • Brändén, M.1    Sandén, T.2    Brzezinski, P.3    Widengren, J.4
  • 74
    • 80052283926 scopus 로고    scopus 로고
    • Protons migrate along interfacial water without significant contributions from jumps between ionizable groups on the membrane surface
    • Springer A, Hagen V, Cherepanov DA, Antonenko YN, Pohl P (2011) Protons migrate along interfacial water without significant contributions from jumps between ionizable groups on the membrane surface. Proc Natl Acad Sci USA 108: 14461-14466
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 14461-14466
    • Springer, A.1    Hagen, V.2    Cherepanov, D.A.3    Antonenko, Y.N.4    Pohl, P.5
  • 76
    • 43049122273 scopus 로고    scopus 로고
    • Water in nonpolar confinement: From nanotubes to proteins and beyond
    • Rasaiah JC, Garde S, Hummer G (2008) Water in nonpolar confinement: from nanotubes to proteins and beyond. Annu Rev Phys Chem 59: 713-740
    • (2008) Annu Rev Phys Chem , vol.59 , pp. 713-740
    • Rasaiah, J.C.1    Garde, S.2    Hummer, G.3
  • 77
    • 2142715470 scopus 로고    scopus 로고
    • Water dynamics and dewetting transitions in the small mechanosensitive channel MscS
    • Anishkin A, Sukharev S (2004) Water dynamics and dewetting transitions in the small mechanosensitive channel MscS. Biophys J 86: 2883-2895
    • (2004) Biophys J , vol.86 , pp. 2883-2895
    • Anishkin, A.1    Sukharev, S.2
  • 78
    • 85028099698 scopus 로고    scopus 로고
    • Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 A °
    • Umena Y, Kawakami K, Shen J-R, Kamiya N (2011) Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 A °. Nature 473: 55-60
    • (2011) Nature , vol.473 , pp. 55-60
    • Umena, Y.1    Kawakami, K.2    Shen, J.-R.3    Kamiya, N.4
  • 79
    • 0025877453 scopus 로고
    • Protein hydration and function
    • Rupley JA, Careri G (1991) Protein hydration and function. Adv Protein Chem 41: 37-172
    • (1991) Adv Protein Chem , vol.41 , pp. 37-172
    • Rupley, J.A.1    Careri, G.2
  • 81
    • 3042592839 scopus 로고    scopus 로고
    • Hydration free energies and entropies for water in protein interiors
    • Olano LR, Rick SW (2004) Hydration free energies and entropies for water in protein interiors. J Am Chem Soc 126: 7991-8000
    • (2004) J Am Chem Soc , vol.126 , pp. 7991-8000
    • Olano, L.R.1    Rick, S.W.2
  • 82
    • 5644282595 scopus 로고    scopus 로고
    • Cooperative motions of protein and hydration water molecules: Molecular dynamics study of scytalone dehydratase
    • Okimoto N, Nakamura T, Suenaga A, Futatsugi N, Hirano Y, Yamaguchi I, Ebisuzaki T (2004) Cooperative motions of protein and hydration water molecules: molecular dynamics study of scytalone dehydratase. J Am Chem Soc 126: 13132-13139
    • (2004) J Am Chem Soc , vol.126 , pp. 13132-13139
    • Okimoto, N.1    Nakamura, T.2    Suenaga, A.3    Futatsugi, N.4    Hirano, Y.5    Yamaguchi, I.6    Ebisuzaki, T.7
  • 83
    • 0037019460 scopus 로고    scopus 로고
    • Molecular dynamics of water at the protein-solvent interface
    • Bizzarri AR, Cannistraro S (2002) Molecular dynamics of water at the protein-solvent interface. J Phys Chem B 106: 6617-6633
    • (2002) J Phys Chem B , vol.106 , pp. 6617-6633
    • Bizzarri, A.R.1    Cannistraro, S.2
  • 85
    • 0026720247 scopus 로고
    • Crystalline ribonuclease A loses function below the dynamical transition at 220 K
    • Rasmussen BF, Stock AM, Ringe D, Petsko GA (1992) Crystalline ribonuclease A loses function below the dynamical transition at 220 K. Nature 357: 423-424
    • (1992) Nature , vol.357 , pp. 423-424
    • Rasmussen, B.F.1    Stock, A.M.2    Ringe, D.3    Petsko, G.A.4
  • 87
    • 19044399611 scopus 로고    scopus 로고
    • Role of protein-water hydrogen bond dynamics in the protein dynamical transition
    • Tarek M, Tobias DJ (2002) Role of protein-water hydrogen bond dynamics in the protein dynamical transition. Phys Rev Lett 88: 138101
    • (2002) Phys Rev Lett , vol.88 , pp. 138101
    • Tarek, M.1    Tobias, D.J.2
  • 89
    • 0042861647 scopus 로고    scopus 로고
    • Translational hydration water dynamics drives the protein glass transition
    • Tournier AL, Xu J, Smith JC (2003) Translational hydration water dynamics drives the protein glass transition. Biophys J 85: 1871-1875
    • (2003) Biophys J , vol.85 , pp. 1871-1875
    • Tournier, A.L.1    Xu, J.2    Smith, J.C.3
  • 92
  • 94
    • 0002635816 scopus 로고    scopus 로고
    • Conformational changes
    • Bloomfield VA, Crothers DM, Tinoco I (eds), Structure, properties and functions. University Science, Sausalito
    • Turner DH (2000) Conformational changes. In: Bloomfield VA, Crothers DM, Tinoco I (eds) Nucleic acids. Structure, properties and functions. University Science, Sausalito, pp 259-334
    • (2000) Nucleic acids , pp. 259-334
    • Turner, D.H.1
  • 95
    • 0037526621 scopus 로고    scopus 로고
    • The structure and dynamics of DNA in the gas phase
    • Rueda M, Kalko SG, Luque FJ, Orozco M (2003) The structure and dynamics of DNA in the gas phase. J Am Chem Soc 125: 8007-8014
    • (2003) J Am Chem Soc , vol.125 , pp. 8007-8014
    • Rueda, M.1    Kalko, S.G.2    Luque, F.J.3    Orozco, M.4
  • 96
    • 33646718178 scopus 로고    scopus 로고
    • Weakly bound water molecules shorten singlestranded DNA
    • Cui S, Albrecht C, Kühner F, Gaub HE (2006) Weakly bound water molecules shorten singlestranded DNA. J Am Chem Soc 128: 6636-6639
    • (2006) J Am Chem Soc , vol.128 , pp. 6636-6639
    • Cui, S.1    Albrecht, C.2    Kühner, F.3    Gaub, H.E.4
  • 97
    • 0020692923 scopus 로고
    • Ordered water structure around a B-DNA dodecamer: A quantitative study
    • Kopka ML, Fratini AV, Drew HR, Dickerson RE (1983) Ordered water structure around a B-DNA dodecamer: a quantitative study. J Mol Biol 163: 129-146
    • (1983) J Mol Biol , vol.163 , pp. 129-146
    • Kopka, M.L.1    Fratini, A.V.2    Drew, H.R.3    Dickerson, R.E.4
  • 98
    • 77953441178 scopus 로고    scopus 로고
    • Ultrafast energy exchange via water-phosphate interactions in hydrated DNA
    • Szyc L, Yang M, Elsaesser T (2010) Ultrafast energy exchange via water-phosphate interactions in hydrated DNA. J Phys Chem B 114: 7951-7957
    • (2010) J Phys Chem B , vol.114 , pp. 7951-7957
    • Szyc, L.1    Yang, M.2    Elsaesser, T.3
  • 99
    • 0026498015 scopus 로고
    • Thermodynamic stoichiometries of participation of water, cations and anions in specific and non-specific binding of lac repressor to DNA: Possible thermodynamic origins of the ‘glutamate effect’ on protein-DNA interactions
    • Ha JH, Capp MW, Hohenwalter MD, Baskerville M, Record MT Jr (1992) Thermodynamic stoichiometries of participation of water, cations and anions in specific and non-specific binding of lac repressor to DNA: possible thermodynamic origins of the ‘glutamate effect’ on protein-DNA interactions. J Mol Biol 228: 252-264
    • (1992) J Mol Biol , vol.228 , pp. 252-264
    • Ha, J.H.1    Capp, M.W.2    Hohenwalter, M.D.3    Baskerville, M.4    Record, M.T.5
  • 100
    • 0027372486 scopus 로고
    • Molecular recognition mediated by bound water: A mechanism for star activity of the restriction enzyme endonuclease EcoRI
    • Robinson CR, Sligar SG (1993) Molecular recognition mediated by bound water: a mechanism for star activity of the restriction enzyme endonuclease EcoRI. J Mol Biol 234: 302-306
    • (1993) J Mol Biol , vol.234 , pp. 302-306
    • Robinson, C.R.1    Sligar, S.G.2
  • 101
    • 23244447015 scopus 로고    scopus 로고
    • Interfacial water as a ‘hydration fingerprint’ in the noncognate complex of BamHI
    • Fuxreiter M, Mezei M, Simon I, Osman R (2005) Interfacial water as a ‘hydration fingerprint’ in the noncognate complex of BamHI. Biophys J 89: 903-911
    • (2005) Biophys J , vol.89 , pp. 903-911
    • Fuxreiter, M.1    Mezei, M.2    Simon, I.3    Osman, R.4
  • 102
    • 33749337783 scopus 로고    scopus 로고
    • Water percolation governs polymorphic transitions and conductivity of DNA
    • Brovchenko I, Krukau A, Oleinikova A, Mazur AK (2006) Water percolation governs polymorphic transitions and conductivity of DNA. Phys Rev Lett 97: 137801
    • (2006) Phys Rev Lett , vol.97 , pp. 137801
    • Brovchenko, I.1    Krukau, A.2    Oleinikova, A.3    Mazur, A.K.4
  • 103
    • 34147187253 scopus 로고    scopus 로고
    • Water clustering and percolation in low hydration DNA shells
    • Brovchenko I, Krukau A, Oleinikova A, Mazur AK (2007) Water clustering and percolation in low hydration DNA shells. J Phys Chem B 111: 3258-3266
    • (2007) J Phys Chem B , vol.111 , pp. 3258-3266
    • Brovchenko, I.1    Krukau, A.2    Oleinikova, A.3    Mazur, A.K.4
  • 104
    • 77957582341 scopus 로고    scopus 로고
    • Changes in the zero-point energy of protons as the source of the binding energy of water to A-phase DNA
    • Reiter GF, Senesi R, Mayers J (2010) Changes in the zero-point energy of protons as the source of the binding energy of water to A-phase DNA. Phys Rev Lett 105: 148101
    • (2010) Phys Rev Lett , vol.105 , pp. 148101
    • Reiter, G.F.1    Senesi, R.2    Mayers, J.3
  • 105
    • 0032387836 scopus 로고    scopus 로고
    • Structure of the potassium form of CGCGAATTCGCG: DNA deformation by electrostatic collapse around inorganic cations
    • Shui X, Sines CC, McFail-Isom L, VanDerveer D, Williams LD (1998) Structure of the potassium form of CGCGAATTCGCG: DNA deformation by electrostatic collapse around inorganic cations. Biochemistry 37: 16877-16887
    • (1998) Biochemistry , vol.37 , pp. 16877-16887
    • Shui, X.1    Sines, C.C.2    McFail-Isom, L.3    VanDerveer, D.4    Williams, L.D.5
  • 106
    • 22144496413 scopus 로고    scopus 로고
    • Does water play a structural role in the folding of small nucleic acids?
    • Sorin EJ, Rhee YM, Pande VS (2005) Does water play a structural role in the folding of small nucleic acids? Biophys J 88: 2516-2524
    • (2005) Biophys J , vol.88 , pp. 2516-2524
    • Sorin, E.J.1    Rhee, Y.M.2    Pande, V.S.3
  • 108
    • 4444275437 scopus 로고    scopus 로고
    • ‘Zur Lehre von der Wikrung der Salze’ (about the science of the effect of salts): Franz Hofmeister’s historical papers
    • Kunz W, Henle J, Ninham BW (2004) ‘Zur Lehre von der Wikrung der Salze’ (about the science of the effect of salts): Franz Hofmeister’s historical papers. Curr Opin Colloid Interface Sci 9: 19-37
    • (2004) Curr Opin Colloid Interface Sci , vol.9 , pp. 19-37
    • Kunz, W.1    Henle, J.2    Ninham, B.W.3
  • 109
    • 40149088818 scopus 로고    scopus 로고
    • Getting specific about specific ion effects
    • Tobias D, Hemminger J (2008) Getting specific about specific ion effects. Science 319: 1197-1198
    • (2008) Science , vol.319 , pp. 1197-1198
    • Tobias, D.1    Hemminger, J.2
  • 110
    • 33646387717 scopus 로고    scopus 로고
    • Specific ion effects at the air/water interface
    • Jungwirth P, Tobias DJ (2006) Specific ion effects at the air/water interface. Chem Rev 106: 1259-1281
    • (2006) Chem Rev , vol.106 , pp. 1259-1281
    • Jungwirth, P.1    Tobias, D.J.2
  • 111
    • 33646732279 scopus 로고    scopus 로고
    • On the nature of ions at the liquid water surface
    • Petersen PB, Saykally RJ (2006) On the nature of ions at the liquid water surface. Annu Rev Phys Chem 57: 333-364
    • (2006) Annu Rev Phys Chem , vol.57 , pp. 333-364
    • Petersen, P.B.1    Saykally, R.J.2
  • 112
    • 33751255662 scopus 로고    scopus 로고
    • Aggregation and dispersion of small hydrophobic particles in aqueous electrolyte solutions
    • Zangi R, Berne BJ (2006) Aggregation and dispersion of small hydrophobic particles in aqueous electrolyte solutions. J Phys Chem B 110: 22736-22741
    • (2006) J Phys Chem B , vol.110 , pp. 22736-22741
    • Zangi, R.1    Berne, B.J.2
  • 113
    • 34247500338 scopus 로고    scopus 로고
    • Effects of ions on the hydrophobic interaction between two plates
    • Zangi R, Hagen M, Berne BJ (2007) Effects of ions on the hydrophobic interaction between two plates. J Am Chem Soc 129: 4678-4686
    • (2007) J Am Chem Soc , vol.129 , pp. 4678-4686
    • Zangi, R.1    Hagen, M.2    Berne, B.J.3
  • 114
  • 117
    • 70350393560 scopus 로고    scopus 로고
    • Strong specific hydroxide ion binding at the pristine oil/water and air/water interfaces
    • Creux P, Lachaise J, Graciaa A, Beattie JK, Djerdjev AM (2009) Strong specific hydroxide ion binding at the pristine oil/water and air/water interfaces. J Phys Chem B 113: 14146-14150
    • (2009) J Phys Chem B , vol.113 , pp. 14146-14150
    • Creux, P.1    Lachaise, J.2    Graciaa, A.3    Beattie, J.K.4    Djerdjev, A.M.5
  • 118
    • 4344568679 scopus 로고    scopus 로고
    • The molecular basis of life: Is life possible without water?
    • Daniel RM, Finney JL, Stoneham M (2004) The molecular basis of life: is life possible without water? Phil Trans R Soc Lond B 359: 1143-1328
    • (2004) Phil Trans R Soc Lond B , vol.359 , pp. 1143-1328
    • Daniel, R.M.1    Finney, J.L.2    Stoneham, M.3


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