메뉴 건너뛰기




Volumn 2, Issue 3, 2008, Pages 390-399

Optimal design of a molecular recognizer: Molecular recognition as a Bayesian signal detection problem

Author keywords

Bayesian detection; Conformational changes; Molecular recognition; Specificity

Indexed keywords

COMPETITION; MOLECULAR BIOLOGY; MOLECULAR RECOGNITION; MOLECULES; NUCLEIC ACIDS; OPTIMAL SYSTEMS; ORGANIC ACIDS; SIGNAL DETECTION; SIGNAL PROCESSING;

EID: 47049095258     PISSN: 19324553     EISSN: None     Source Type: Journal    
DOI: 10.1109/JSTSP.2008.923859     Document Type: Article
Times cited : (11)

References (26)
  • 1
    • 0001971367 scopus 로고
    • L. Pauling, Science, vol. 92, pp. 77-79, 1940.
    • (1940) Science , vol.92 , pp. 77-79
    • Pauling, L.1
  • 2
    • 0008863560 scopus 로고
    • Some factors in the interpretation of protein denaturation
    • W. Kauzmann, "Some factors in the interpretation of protein denaturation," Adv. Protein Chem., vol. 14, pp. 1-63, 1959.
    • (1959) Adv. Protein Chem , vol.14 , pp. 1-63
    • Kauzmann, W.1
  • 3
    • 0018318966 scopus 로고
    • Interfacial free energy and the hydrophobic effect
    • C. Tanford, "Interfacial free energy and the hydrophobic effect," Proc. Nat. Acad. Sci. USA, vol. 76, pp. 4175-4176, 1979.
    • (1979) Proc. Nat. Acad. Sci. USA , vol.76 , pp. 4175-4176
    • Tanford, C.1
  • 4
    • 42449120195 scopus 로고    scopus 로고
    • A simple model for the evolution of molecular codes driven by the interplay of accuracy, diversity and cost
    • T. Tlusty, "A simple model for the evolution of molecular codes driven by the interplay of accuracy, diversity and cost," Phys. Biol., vol. 5, p. 016001, 2008.
    • (2008) Phys. Biol , vol.5 , pp. 016001
    • Tlusty, T.1
  • 5
    • 38749149160 scopus 로고    scopus 로고
    • Rate-distortion scenario for the emergence and evolution of noisy molecular codes
    • T. Tlusty, "Rate-distortion scenario for the emergence and evolution of noisy molecular codes," Phys. Rev. Lett., vol. 100, pp. 048101-048104, 2008.
    • (2008) Phys. Rev. Lett , vol.100 , pp. 048101-048104
    • Tlusty, T.1
  • 6
    • 0037008011 scopus 로고    scopus 로고
    • Multiple conformational changes in enzyme catalysis
    • G. G. Hammes, "Multiple conformational changes in enzyme catalysis," Biochemistry, vol. 41, pp. 8221-8228, 2002.
    • (2002) Biochemistry , vol.41 , pp. 8221-8228
    • Hammes, G.G.1
  • 8
    • 24644521419 scopus 로고    scopus 로고
    • Structure and kinetics of a transient antibody binding intermediate reveal a kinetic discrimination mechanism in antigen recognition
    • L. C. James and D. S. Tawfik, "Structure and kinetics of a transient antibody binding intermediate reveal a kinetic discrimination mechanism in antigen recognition," Proc. Nat. Acad. USA, vol. 102, pp. 12730-12735, 2005.
    • (2005) Proc. Nat. Acad. USA , vol.102 , pp. 12730-12735
    • James, L.C.1    Tawfik, D.S.2
  • 9
    • 0030028728 scopus 로고    scopus 로고
    • Principles of protein-protein interactions
    • S. Jones and J. M. Thornton, "Principles of protein-protein interactions," Proc. Nat. Acad. USA, vol. 93, pp. 13-20, 1996.
    • (1996) Proc. Nat. Acad. USA , vol.93 , pp. 13-20
    • Jones, S.1    Thornton, J.M.2
  • 10
    • 1342302339 scopus 로고    scopus 로고
    • Conformational changes associated with protein-protein interactions
    • C. S. Goh, D. Milburn, and M. Gerstein, "Conformational changes associated with protein-protein interactions," Curr. Opin. Struct. Biol., vol. 14, pp. 104-109, 2004.
    • (2004) Curr. Opin. Struct. Biol , vol.14 , pp. 104-109
    • Goh, C.S.1    Milburn, D.2    Gerstein, M.3
  • 11
    • 0021196998 scopus 로고
    • Protein-DNA recognition
    • C. O. Pabo and R. T. Sauer, "Protein-DNA recognition," Annu. Rev. Biochem., vol. 53, pp. 293-321, 1984.
    • (1984) Annu. Rev. Biochem , vol.53 , pp. 293-321
    • Pabo, C.O.1    Sauer, R.T.2
  • 12
    • 0027220197 scopus 로고
    • Conformational coupling in DNA polymerase fidelity
    • 15
    • K. A. Johnson, "Conformational coupling in DNA polymerase fidelity," Annu. Rev. Biochem., vol. 62, pp. 685-713, 1993, [15].
    • (1993) Annu. Rev. Biochem , vol.62 , pp. 685-713
    • Johnson, K.A.1
  • 13
    • 0033784534 scopus 로고    scopus 로고
    • Induced fit in RNA-protein recognition
    • J. R. Williamson, "Induced fit in RNA-protein recognition," Nat. Struct. Biol., vol. 7, pp. 834-837, 2000.
    • (2000) Nat. Struct. Biol , vol.7 , pp. 834-837
    • Williamson, J.R.1
  • 14
    • 0016232066 scopus 로고
    • Catalysis, binding and enzyme-substrate complementarity
    • A. R. Fersht, "Catalysis, binding and enzyme-substrate complementarity," Proc. Roy. Soc. Lond. B, Biol. Sci., vol. 187, pp. 397-407, 1974.
    • (1974) Proc. Roy. Soc. Lond. B, Biol. Sci , vol.187 , pp. 397-407
    • Fersht, A.R.1
  • 16
    • 0028839740 scopus 로고    scopus 로고
    • C. B. Post and W. J. Ray, Jr., Reexamination of induced fit as a determinant of substrate specificity in enzymatic reactions, Biochemistry, 34, pp. 15881-15885, 1995.
    • C. B. Post and W. J. Ray, Jr., "Reexamination of induced fit as a determinant of substrate specificity in enzymatic reactions," Biochemistry, vol. 34, pp. 15881-15885, 1995.
  • 17
    • 55849099561 scopus 로고    scopus 로고
    • Conformational proofreading: The impact of conformational changes on the specificity of molecular recognition
    • Y. Savir and T. Tlusty, "Conformational proofreading: The impact of conformational changes on the specificity of molecular recognition," PLoS ONE, vol. 2, p. e468, 2007.
    • (2007) PLoS ONE , vol.2
    • Savir, Y.1    Tlusty, T.2
  • 18
    • 0002724139 scopus 로고
    • The role of induced fit and conformational changes of enzymes in specificity and catalysis
    • D. Herschlag, "The role of induced fit and conformational changes of enzymes in specificity and catalysis," Bioorg. Chem., vol. 16, pp. 62-96, 1988.
    • (1988) Bioorg. Chem , vol.16 , pp. 62-96
    • Herschlag, D.1
  • 20
    • 0000197372 scopus 로고    scopus 로고
    • Large amplitude elastic motions in proteins from a single-parameter, atomic analysis
    • M. M. Tirion, "Large amplitude elastic motions in proteins from a single-parameter, atomic analysis," Phys. Rev. Lett., vol. 77, pp. 1905-1908, 1996.
    • (1996) Phys. Rev. Lett , vol.77 , pp. 1905-1908
    • Tirion, M.M.1
  • 21
    • 0030623823 scopus 로고    scopus 로고
    • Direct evaluation of thermal fluctuations in proteins using a single-parameter harmonic potential
    • I. Bahar, A. R. Atilgan, and B. Erman, "Direct evaluation of thermal fluctuations in proteins using a single-parameter harmonic potential," Fold Des., vol. 2, pp. 173-181, 1997.
    • (1997) Fold Des , vol.2 , pp. 173-181
    • Bahar, I.1    Atilgan, A.R.2    Erman, B.3
  • 22
    • 0035044995 scopus 로고    scopus 로고
    • Conformational change of proteins arising from normal mode calculations
    • F. Tama and Y. H. Sanejouand, "Conformational change of proteins arising from normal mode calculations," Protein Eng., vol. 14, pp. 1-6, 2001.
    • (2001) Protein Eng , vol.14 , pp. 1-6
    • Tama, F.1    Sanejouand, Y.H.2
  • 23
    • 30044434744 scopus 로고    scopus 로고
    • Structural changes involved in protein binding correlate with intrinsic motions of proteins in the unbound state
    • D. Tobi and I. Bahar, "Structural changes involved in protein binding correlate with intrinsic motions of proteins in the unbound state," Proc. Nat. Acad. USA, vol. 102, pp. 18908-18913, 2005.
    • (2005) Proc. Nat. Acad. USA , vol.102 , pp. 18908-18913
    • Tobi, D.1    Bahar, I.2
  • 25
    • 0004155427 scopus 로고
    • 3rd ed. New York: Freeman
    • L. Stryer, Biochemistry, 3rd ed. New York: Freeman, 1988.
    • (1988) Biochemistry
    • Stryer, L.1
  • 26
    • 47049105334 scopus 로고    scopus 로고
    • DNA extension induced by RecA during homologous recombination as a possible conformational proofreading mechanism
    • to be published
    • Y. Savir and T. Tlusty, "DNA extension induced by RecA during homologous recombination as a possible conformational proofreading mechanism," to be published.
    • Savir, Y.1    Tlusty, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.