메뉴 건너뛰기




Volumn 1724, Issue 3, 2005, Pages 411-424

Dominant features of protein reaction dynamics: Conformational relaxation and ligand migration

Author keywords

Hemoproteins; Kinetics of rebinding; Laser photolysis; Ligand migration; Protein dynamics; Protein relaxation

Indexed keywords

CARBON MONOXIDE; CYTOCHROME P450; HEMOPROTEIN; LIGAND; MYOGLOBIN; XENON;

EID: 23144435806     PISSN: 03044165     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbagen.2005.04.024     Document Type: Review
Times cited : (17)

References (55)
  • 2
    • 0028982472 scopus 로고
    • Viscosity dependence of O2 escape from respiratory proteins as a function of cosolvent molecular weight
    • S. Yedgar, C. Tetreau, B. Gavish, and D. Lavalette Viscosity dependence of O2 escape from respiratory proteins as a function of cosolvent molecular weight Biophys. J. 68 1995 665 670
    • (1995) Biophys. J. , vol.68 , pp. 665-670
    • Yedgar, S.1    Tetreau, C.2    Gavish, B.3    Lavalette, D.4
  • 3
    • 0004241418 scopus 로고
    • Academic Press Inc., Ltd. London
    • P. Douzou Cryobiochemistry 1977 Academic Press Inc., Ltd. London
    • (1977) Cryobiochemistry
    • Douzou, P.1
  • 5
    • 85047689690 scopus 로고
    • Viscosity-dependent energy barriers and equilibrium conformational fluctuations in oxygen recombination with Hemerythrin
    • D. Lavalette, and C. Tetreau Viscosity-dependent energy barriers and equilibrium conformational fluctuations in oxygen recombination with Hemerythrin Eur. J. Biochem. 177 1988 97 108
    • (1988) Eur. J. Biochem. , vol.177 , pp. 97-108
    • Lavalette, D.1    Tetreau, C.2
  • 7
    • 0030058805 scopus 로고    scopus 로고
    • Two-dimensional distributions of activation enthalpy and entropy from kinetics by the maximum entropy method
    • P.J. Steinbach Two-dimensional distributions of activation enthalpy and entropy from kinetics by the maximum entropy method Biophys. J. 70 1996 1521 1528
    • (1996) Biophys. J. , vol.70 , pp. 1521-1528
    • Steinbach, P.J.1
  • 9
    • 0034700241 scopus 로고    scopus 로고
    • Conformational relaxation in hemoproteins: The cytochrome P450cam case
    • C. Tetreau, M. Tourbez, and D. Lavalette Conformational relaxation in hemoproteins: the cytochrome P450cam case Biochemistry 39 2000 14219 14231
    • (2000) Biochemistry , vol.39 , pp. 14219-14231
    • Tetreau, C.1    Tourbez, M.2    Lavalette, D.3
  • 11
    • 0001464493 scopus 로고
    • Analyzing the distribution of decay constants in pulse-fluorimetry using the maximum entropy method
    • A.K. Livesey, and J.-C. Brochon Analyzing the distribution of decay constants in pulse-fluorimetry using the maximum entropy method Biophys. J. 52 1987 693 706
    • (1987) Biophys. J. , vol.52 , pp. 693-706
    • Livesey, A.K.1    Brochon, J.-C.2
  • 14
    • 0027371191 scopus 로고
    • Dynamics of protein relaxation in site-specific mutants of human myoglobin
    • D.G. Lambright, S. Balasubramanian, and S.G. Boxer Dynamics of protein relaxation in site-specific mutants of human myoglobin Biochemistry 32 1993 10116 10124
    • (1993) Biochemistry , vol.32 , pp. 10116-10124
    • Lambright, D.G.1    Balasubramanian, S.2    Boxer, S.G.3
  • 15
    • 0029762039 scopus 로고    scopus 로고
    • Ligand binding to heme proteins: VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin
    • J.B. Johnson, D.C. Lamb, H. Frauenfelder, J.D. Müller, B. McMahon, and G.U. Nienhaus Ligand binding to heme proteins: VI. Interconversion of taxonomic substates in carbonmonoxymyoglobin Biophys. J. 71 1996 1563 1573
    • (1996) Biophys. J. , vol.71 , pp. 1563-1573
    • Johnson, J.B.1    Lamb, D.C.2    Frauenfelder, H.3    Müller, J.D.4    McMahon, B.5    Nienhaus, G.U.6
  • 16
    • 0346057931 scopus 로고    scopus 로고
    • Competition with xenon elicits ligand migration and escape pathways in myoglobin
    • C. Tetreau, Y. Blouquit, E. Novikov, E. Quiniou, and D. Lavalette Competition with xenon elicits ligand migration and escape pathways in myoglobin Biophys. J. 86 2004 435 447
    • (2004) Biophys. J. , vol.86 , pp. 435-447
    • Tetreau, C.1    Blouquit, Y.2    Novikov, E.3    Quiniou, E.4    Lavalette, D.5
  • 19
    • 0030768765 scopus 로고    scopus 로고
    • Ligand migration in sperm whale myoglobin
    • E.E. Scott, and Q.H. Gibson Ligand migration in sperm whale myoglobin Biochemistry 36 1997 11909 11917
    • (1997) Biochemistry , vol.36 , pp. 11909-11917
    • Scott, E.E.1    Gibson, Q.H.2
  • 20
    • 0035895937 scopus 로고    scopus 로고
    • Mapping the pathways for O2 entry into and exit from myoglobin
    • E.E. Scott, Q.H. Gibson, and J.S. Olson Mapping the pathways for O2 entry into and exit from myoglobin J. Biol. Chem. 276 2001 5177 5188
    • (2001) J. Biol. Chem. , vol.276 , pp. 5177-5188
    • Scott, E.E.1    Gibson, Q.H.2    Olson, J.S.3
  • 25
    • 0035923445 scopus 로고    scopus 로고
    • Protein conformational relaxation and ligand migration in myoglobin: A nanosecond to millisecond movie from time-resolved Laue X-ray diffraction
    • V. Srajer, Z. Ren, T.-Y. Teng, M. Schmidt, T. Ursby, D. Bourgeois, C. Pradervand, W. Schildkamp, M. Wulff, and K. Moffat Protein conformational relaxation and ligand migration in myoglobin: a nanosecond to millisecond movie from time-resolved Laue X-ray diffraction Biochemistry 40 2001 13802 13815
    • (2001) Biochemistry , vol.40 , pp. 13802-13815
    • Srajer, V.1    Ren, Z.2    Teng, T.-Y.3    Schmidt, M.4    Ursby, T.5    Bourgeois, D.6    Pradervand, C.7    Schildkamp, W.8    Wulff, M.9    Moffat, K.10
  • 29
    • 0038853525 scopus 로고    scopus 로고
    • Crystal structures of myoglobin-ligand complexes at near-atomic resolution
    • J. Vojtechovsky, K. Chu, J. Berendzen, R.M. Sweet, and I. Schlichting Crystal structures of myoglobin-ligand complexes at near-atomic resolution Biophys. J. 77 1999 2153 2174
    • (1999) Biophys. J. , vol.77 , pp. 2153-2174
    • Vojtechovsky, J.1    Chu, K.2    Berendzen, J.3    Sweet, R.M.4    Schlichting, I.5
  • 30
    • 0029986887 scopus 로고    scopus 로고
    • Crystal structures of CO-, deoxy- and met-myoglobins at various pH values
    • F. Yang, and J.G.N. Phillips Crystal structures of CO-, deoxy- and met-myoglobins at various pH values J. Mol. Biol. 256 1996 762 774
    • (1996) J. Mol. Biol. , vol.256 , pp. 762-774
    • Yang, F.1    Phillips, J.G.N.2
  • 32
    • 0023275103 scopus 로고
    • Oxygen infrared spectra of oxyhemoglobins and oxymyoglobins. Evidence of two major liganded O2 structures
    • W.T. Potter, M.P. Tucker, R.A. Houtchens, and W.S. Caughey Oxygen infrared spectra of oxyhemoglobins and oxymyoglobins. Evidence of two major liganded O2 structures Biochemistry 26 1987 4699 4707
    • (1987) Biochemistry , vol.26 , pp. 4699-4707
    • Potter, W.T.1    Tucker, M.P.2    Houtchens, R.A.3    Caughey, W.S.4
  • 33
    • 0036214745 scopus 로고    scopus 로고
    • Kinetic evidence for three photolyzable taxonomic conformational substates in oxymyoglobin
    • C. Tetreau, E. Novikov, M. Tourbez, and D. Lavalette Kinetic evidence for three photolyzable taxonomic conformational substates in oxymyoglobin Biophys. J. 82 2002 2148 2155
    • (2002) Biophys. J. , vol.82 , pp. 2148-2155
    • Tetreau, C.1    Novikov, E.2    Tourbez, M.3    Lavalette, D.4
  • 35
    • 0000503621 scopus 로고
    • Dynamic behavior of the active site structure in bacterial cytochrome P-450
    • C. Jung, and F. Marlow Dynamic behavior of the active site structure in bacterial cytochrome P-450 Stud. Biophys. 120 1987 241 251
    • (1987) Stud. Biophys. , vol.120 , pp. 241-251
    • Jung, C.1    Marlow, F.2
  • 36
    • 0030067240 scopus 로고    scopus 로고
    • The CO stretching mode infrared spectrum of substrate-free cytochrome P-450cam-CO. the effect of solvent conditions, temperature and pressure
    • C. Jung, O. Ristau, H. Schulze, and S.G. Sligar The CO stretching mode infrared spectrum of substrate-free cytochrome P-450cam-CO. The effect of solvent conditions, temperature and pressure Eur. Biochem. J. 235 1996 660 669
    • (1996) Eur. Biochem. J. , vol.235 , pp. 660-669
    • Jung, C.1    Ristau, O.2    Schulze, H.3    Sligar, S.G.4
  • 37
    • 0033151781 scopus 로고    scopus 로고
    • Dynamics of carbon monoxide binding with neuronal nitric oxide synthase
    • C. Tetreau, M. Tourbez, A. Gorren, B. Mayer, and D. Lavalette Dynamics of carbon monoxide binding with neuronal nitric oxide synthase Biochemistry 38 1999 7210 7218
    • (1999) Biochemistry , vol.38 , pp. 7210-7218
    • Tetreau, C.1    Tourbez, M.2    Gorren, A.3    Mayer, B.4    Lavalette, D.5
  • 38
    • 0023645035 scopus 로고
    • High-resolution crystal structure of cytochrome P450cam
    • T.L. Poulos, B.C. Finzel, and A.J. Howard High-resolution crystal structure of cytochrome P450cam J. Mol. Biol. 195 1987 687 700
    • (1987) J. Mol. Biol. , vol.195 , pp. 687-700
    • Poulos, T.L.1    Finzel, B.C.2    Howard, A.J.3
  • 39
    • 0024974060 scopus 로고
    • Crystal structure of the carbon-monoxide-substrate-cytochrome P-450cam ternary complex
    • R. Raag, and T.L. Poulos Crystal structure of the carbon-monoxide- substrate-cytochrome P-450cam ternary complex Biochemistry 28 1989 7586 7592
    • (1989) Biochemistry , vol.28 , pp. 7586-7592
    • Raag, R.1    Poulos, T.L.2
  • 40
    • 0034624691 scopus 로고    scopus 로고
    • Ligand binding and conformational motions in myoglobin
    • A. Ostermann, R. Waschipky, F.G. Parak, and G.U. Nienhaus Ligand binding and conformational motions in myoglobin Nature 404 2000 205 208
    • (2000) Nature , vol.404 , pp. 205-208
    • Ostermann, A.1    Waschipky, R.2    Parak, F.G.3    Nienhaus, G.U.4
  • 41
    • 0021766921 scopus 로고
    • Cavities in proteins: Structure of a metmyoglobin-xenon complex solved to 1.9 Å
    • R.F. Tilton, I.D. Kuntz, and G.A. Petsko Cavities in proteins: structure of a metmyoglobin-xenon complex solved to 1.9 Å Biochemistry 23 1984 2849 2857
    • (1984) Biochemistry , vol.23 , pp. 2849-2857
    • Tilton, R.F.1    Kuntz, I.D.2    Petsko, G.A.3
  • 42
    • 0033019674 scopus 로고    scopus 로고
    • Structural dynamics of ligand diffusion in the protein matrix: A study on a new myoglobin mutant Y(B10) Q(E7) R(E10)
    • M. Brunori, F. Cutruzzola, C. Savino, C. Travaglini-Allocatelli, B. Vallone, and Q.H. Gibson Structural dynamics of ligand diffusion in the protein matrix: a study on a new myoglobin mutant Y(B10) Q(E7) R(E10) Biophys. J. 76 1999 1259 1269
    • (1999) Biophys. J. , vol.76 , pp. 1259-1269
    • Brunori, M.1    Cutruzzola, F.2    Savino, C.3    Travaglini-Allocatelli, C.4    Vallone, B.5    Gibson, Q.H.6
  • 44
    • 0035119236 scopus 로고    scopus 로고
    • Ligand migration in human myoglobin: Steric effects of isoleucine 107(G8) on O2 and CO binding
    • H. Ishikawa, T. Uchida, S. Takahashi, K. Ishimori, and I. Morishima Ligand migration in human myoglobin: steric effects of isoleucine 107(G8) on O2 and CO binding Biophys. J. 80 2001 1507 1517
    • (2001) Biophys. J. , vol.80 , pp. 1507-1517
    • Ishikawa, H.1    Uchida, T.2    Takahashi, S.3    Ishimori, K.4    Morishima, I.5
  • 46
    • 0027953943 scopus 로고
    • Nitric oxide recombination to double mutants of myoglobin: Role of ligand diffusion in a fluctuating heme pocket
    • M.L. Carlson, R. Regan, R. Elber, H. Li, G.N. Phillips, J.S. Olson, and Q.H. Gibson Nitric oxide recombination to double mutants of myoglobin: role of ligand diffusion in a fluctuating heme pocket Biochemistry 33 1994 10597 10606
    • (1994) Biochemistry , vol.33 , pp. 10597-10606
    • Carlson, M.L.1    Regan, R.2    Elber, R.3    Li, H.4    Phillips, G.N.5    Olson, J.S.6    Gibson, Q.H.7
  • 47
    • 0025600834 scopus 로고
    • Enhanced sampling in molecular dynamics: Use of the time-dependent Hartree approximation for a simulation of carbon monoxide diffusion through myoglobin
    • R. Elber, and M. Karplus Enhanced sampling in molecular dynamics: use of the time-dependent Hartree approximation for a simulation of carbon monoxide diffusion through myoglobin J. Am. Chem. Soc. 112 1990 9161 9175
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 9161-9175
    • Elber, R.1    Karplus, M.2
  • 48
    • 0026526264 scopus 로고
    • Distal pocket residues affect picosecond ligand recombination in myoglobin
    • Q.H. Gibson, R. Regan, R. Elber, J.S. Olson, and T.E. Carver Distal pocket residues affect picosecond ligand recombination in myoglobin J. Biol. Chem. 267 1992 22022 22034
    • (1992) J. Biol. Chem. , vol.267 , pp. 22022-22034
    • Gibson, Q.H.1    Regan, R.2    Elber, R.3    Olson, J.S.4    Carver, T.E.5
  • 49
    • 0027202194 scopus 로고
    • Molecular dynamics simulation of NO recombination to myoglobin mutants
    • H. Li, R. Elber, and J.E. Straub Molecular dynamics simulation of NO recombination to myoglobin mutants J. Biol. Chem. 268 1993 17908 17916
    • (1993) J. Biol. Chem. , vol.268 , pp. 17908-17916
    • Li, H.1    Elber, R.2    Straub, J.E.3
  • 50
    • 0030031593 scopus 로고    scopus 로고
    • Distal cavity fluctuations in myoglobin: Protein motion and ligand diffusion
    • M.L. Carlson, R.M. Regan, and Q.H. Gibson Distal cavity fluctuations in myoglobin: protein motion and ligand diffusion Biochemistry 35 1996 1125 1136
    • (1996) Biochemistry , vol.35 , pp. 1125-1136
    • Carlson, M.L.1    Regan, R.M.2    Gibson, Q.H.3
  • 51
    • 0042242570 scopus 로고    scopus 로고
    • Structural dynamics of myoglobin: Spectroscopic and structural characterization of ligand docking sites in myoglobin mutant L29W
    • K. Nienhaus, P. Deng, J.M. Kriegl, and G.U. Nienhaus Structural dynamics of myoglobin: spectroscopic and structural characterization of ligand docking sites in myoglobin mutant L29W Biochemistry 42 2003 9633 9646
    • (2003) Biochemistry , vol.42 , pp. 9633-9646
    • Nienhaus, K.1    Deng, P.2    Kriegl, J.M.3    Nienhaus, G.U.4
  • 52
    • 0041742184 scopus 로고    scopus 로고
    • Structural dynamics of myoglobin: Effect of internal cavities on ligand migration and binding
    • K. Nienhaus, P. Deng, J.M. Kriegl, and G.U. Nienhaus Structural dynamics of myoglobin: effect of internal cavities on ligand migration and binding Biochemistry 42 2003 9647 9658
    • (2003) Biochemistry , vol.42 , pp. 9647-9658
    • Nienhaus, K.1    Deng, P.2    Kriegl, J.M.3    Nienhaus, G.U.4
  • 53
    • 0020842533 scopus 로고
    • Nanosecond flash photolysis study of carbon monoxide binding to the b chain of hemoglobin Zürich [b63(E7)His→Arg]
    • D.D. Dlott, H. Frauenfelder, P. Langer, H. Roder, and E.E. DiIorio Nanosecond flash photolysis study of carbon monoxide binding to the b chain of hemoglobin Zürich [b63(E7)His→Arg] Proc. Natl. Acad. Sci. U. S. A. 80 1983 6239 6243
    • (1983) Proc. Natl. Acad. Sci. U. S. A. , vol.80 , pp. 6239-6243
    • Dlott, D.D.1    Frauenfelder, H.2    Langer, P.3    Roder, H.4    Diiorio, E.E.5
  • 54
    • 0032512436 scopus 로고    scopus 로고
    • Solvent composition and viscosity effects on the kinetics of CO binding to horse myoglobin
    • T. Kleinert, W. Doster, H. Leyser, W. Petry, V. Schwarz, and M. Settles Solvent composition and viscosity effects on the kinetics of CO binding to horse myoglobin Biochemistry 37 1998 717 733
    • (1998) Biochemistry , vol.37 , pp. 717-733
    • Kleinert, T.1    Doster, W.2    Leyser, H.3    Petry, W.4    Schwarz, V.5    Settles, M.6
  • 55
    • 7444230904 scopus 로고    scopus 로고
    • Unveiling functional protein motions with picosecond X-ray crystallography and molecular dynamics simulations
    • G. Hummer, F. Schotte, and P.A. Anfinrud Unveiling functional protein motions with picosecond X-ray crystallography and molecular dynamics simulations Proc. Natl. Acad. Sci. U. S. A. 101 2004 15330 15334
    • (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , pp. 15330-15334
    • Hummer, G.1    Schotte, F.2    Anfinrud, P.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.