메뉴 건너뛰기




Volumn 28, Issue 5, 2014, Pages 530-543

Avidity and positive allosteric modulation/cooperativity act hand in hand to increase the residence time of bivalent receptor ligands

Author keywords

Avidity; Binding kinetics; Bitopic; Bivalent; Cooperativity; Differential equations; Residence time; Simulations

Indexed keywords

ALLOSTERISM; ARTICLE; BINDING AFFINITY; INCUBATION TIME; INTERNALIZATION; LIGAND BINDING; PHARMACOPHORE; PRIORITY JOURNAL; RECEPTOR DOWN REGULATION; SIMULATION; HUMAN; KINETICS; MOLECULAR DYNAMICS;

EID: 84927574644     PISSN: 07673981     EISSN: 14728206     Source Type: Journal    
DOI: 10.1111/fcp.12052     Document Type: Article
Times cited : (13)

References (46)
  • 1
    • 4544381198 scopus 로고    scopus 로고
    • Biochemical mechanisms of drug action: what does it take for success?
    • Swinney D.C. Biochemical mechanisms of drug action: what does it take for success? Nat. Rev. Drug. Discov. (2004) 3 801-808.
    • (2004) Nat. Rev. Drug. Discov. , vol.3 , pp. 801-808
    • Swinney, D.C.1
  • 2
    • 33646122469 scopus 로고    scopus 로고
    • Biochemical mechanisms of new molecular entities (NMEs) approved by United States FDA during 2001-2004: mechanisms leading to optimal efficacy and safety
    • Swinney D.C. Biochemical mechanisms of new molecular entities (NMEs) approved by United States FDA during 2001-2004: mechanisms leading to optimal efficacy and safety. Curr. Top. Med. Chem. (2006) 6 461-478.
    • (2006) Curr. Top. Med. Chem. , vol.6 , pp. 461-478
    • Swinney, D.C.1
  • 3
    • 33749623857 scopus 로고    scopus 로고
    • Can binding kinetics translate to a clinically differentiated drug? From theory to practice
    • Swinney D.C. Can binding kinetics translate to a clinically differentiated drug? From theory to practice. Lett. Drug. Des. Disc. (2006) 3 569-574.
    • (2006) Lett. Drug. Des. Disc. , vol.3 , pp. 569-574
    • Swinney, D.C.1
  • 4
    • 58449131873 scopus 로고    scopus 로고
    • The role of binding kinetics in therapeutically useful drug action
    • Swinney D.C. The role of binding kinetics in therapeutically useful drug action. Curr. Opin. Drug. Discovery. Dev. (2009) 12 31-39.
    • (2009) Curr. Opin. Drug. Discovery. Dev. , vol.12 , pp. 31-39
    • Swinney, D.C.1
  • 5
    • 33748325882 scopus 로고    scopus 로고
    • Drug-target residence time and its implications for lead optimization
    • Copeland R.A., Pompliano D.L., Meek T.D. Drug-target residence time and its implications for lead optimization. Nat. Rev. Drug. Discov. (2006) 5 730-739.
    • (2006) Nat. Rev. Drug. Discov. , vol.5 , pp. 730-739
    • Copeland, R.A.1    Pompliano, D.L.2    Meek, T.D.3
  • 6
    • 44049103958 scopus 로고    scopus 로고
    • Residence time of receptor-ligand complexes and its effect on biological function
    • Tummino P.J., Copeland R.A. Residence time of receptor-ligand complexes and its effect on biological function. Biochemistry (2008) 47 5481-5492.
    • (2008) Biochemistry , vol.47 , pp. 5481-5492
    • Tummino, P.J.1    Copeland, R.A.2
  • 7
    • 77950197835 scopus 로고    scopus 로고
    • The dynamics of drug-target interactions: drug-target residence time and its impact on efficacy and safety Expert
    • Copeland R.A. The dynamics of drug-target interactions: drug-target residence time and its impact on efficacy and safety Expert. Opin. Drug. Discov. (2010) 5 305-510.
    • (2010) Opin. Drug. Discov. , vol.5 , pp. 305-510
    • Copeland, R.A.1
  • 8
    • 67649973722 scopus 로고    scopus 로고
    • The importance of drug-target residence time
    • Zhang R., Monsma F. The importance of drug-target residence time. Curr. Opin. Drug Discov. Devel. (2009) 12 488-496.
    • (2009) Curr. Opin. Drug Discov. Devel. , vol.12 , pp. 488-496
    • Zhang, R.1    Monsma, F.2
  • 9
    • 77949875945 scopus 로고    scopus 로고
    • Effects of losartan vs candesartan in reducing cardiovascular events in the primary treatment of hypertension
    • Kjeldsen S.E., Stålhammar J., Hasvold P., Bodegard J., Olsson U., Russell D. Effects of losartan vs candesartan in reducing cardiovascular events in the primary treatment of hypertension. J. Hum. Hypertens. (2010) 24 263-273.
    • (2010) J. Hum. Hypertens. , vol.24 , pp. 263-273
    • Kjeldsen, S.E.1    Stålhammar, J.2    Hasvold, P.3    Bodegard, J.4    Olsson, U.5    Russell, D.6
  • 11
    • 66249109940 scopus 로고    scopus 로고
    • Affinity and avidity an antibody-based tumor targeting
    • Rudnick S.I., Adams G.P. Affinity and avidity an antibody-based tumor targeting. Cancer Biotherap. Radiopharm. (2009) 24 155-161.
    • (2009) Cancer Biotherap. Radiopharm. , vol.24 , pp. 155-161
    • Rudnick, S.I.1    Adams, G.P.2
  • 12
    • 27144432842 scopus 로고    scopus 로고
    • Engineered antibody fragments and the rise of single domains
    • Holliger P., Hudson P.J. Engineered antibody fragments and the rise of single domains. Nat. Biotechnol. (2005) 23 1126-1136.
    • (2005) Nat. Biotechnol. , vol.23 , pp. 1126-1136
    • Holliger, P.1    Hudson, P.J.2
  • 13
    • 84855879360 scopus 로고    scopus 로고
    • The best of two worlds? Bitopic orthosteric/allosteric ligands of G protein-coupled receptors
    • Valant C., Lane J.R., Sexton P.M., Christopoulos A. The best of two worlds? Bitopic orthosteric/allosteric ligands of G protein-coupled receptors. Annu. Rev. Pharmacol. Toxicol. (2012) 52 153-178.
    • (2012) Annu. Rev. Pharmacol. Toxicol. , vol.52 , pp. 153-178
    • Valant, C.1    Lane, J.R.2    Sexton, P.M.3    Christopoulos, A.4
  • 14
    • 0032476812 scopus 로고    scopus 로고
    • Polyvalent interactions in biological systems: implications for design and use of multivalent ligands and inhibitors
    • Mammen M., Choi S.-K., Whitesides G.M. Polyvalent interactions in biological systems: implications for design and use of multivalent ligands and inhibitors. Angewandte Chemie Int. Ed. (1998) 37 2754-2794.
    • (1998) Angewandte Chemie Int. Ed. , vol.37 , pp. 2754-2794
    • Mammen, M.1    Choi, S.-K.2    Whitesides, G.M.3
  • 15
    • 84875459594 scopus 로고    scopus 로고
    • Exploring avidity, understanding the potential gains in functional affinity and target residence time of bivalent and heterobivalent ligands
    • Vauquelin G., Charlton S. Exploring avidity, understanding the potential gains in functional affinity and target residence time of bivalent and heterobivalent ligands. Br. J. Pharmacol. (2013) 168 1771-1785.
    • (2013) Br. J. Pharmacol. , vol.168 , pp. 1771-1785
    • Vauquelin, G.1    Charlton, S.2
  • 16
    • 0032531947 scopus 로고    scopus 로고
    • Spanning binding sites on allosteric proteins with polymer-linked ligand dimers
    • Kramer R.H., Karpen J.W. Spanning binding sites on allosteric proteins with polymer-linked ligand dimers. Nature (1998) 395 710-713.
    • (1998) Nature , vol.395 , pp. 710-713
    • Kramer, R.H.1    Karpen, J.W.2
  • 17
    • 0026705890 scopus 로고
    • Effect of bivalent interaction upon apparent antibody affinity, Experimental confirmation of a theory using fluorescence photobleaching and implications for antibody binding assays
    • Kaufman E.N., Jain R.K. Effect of bivalent interaction upon apparent antibody affinity, Experimental confirmation of a theory using fluorescence photobleaching and implications for antibody binding assays. Cancer Res. (1992) 52 4157-4167.
    • (1992) Cancer Res. , vol.52 , pp. 4157-4167
    • Kaufman, E.N.1    Jain, R.K.2
  • 18
    • 0030738617 scopus 로고    scopus 로고
    • New protein engineering approaches to multivalent and bispecific antibody fragments
    • Plückthun A., Pack P. New protein engineering approaches to multivalent and bispecific antibody fragments. Immunotechnology (1997) 3 83-105.
    • (1997) Immunotechnology , vol.3 , pp. 83-105
    • Plückthun, A.1    Pack, P.2
  • 19
    • 84862847461 scopus 로고    scopus 로고
    • Radioligand dissociation measurements, potential interference of rebinding and allosteric mechanisms and physiological relevance of the biological model systems
    • Vauquelin G., Van Liefde I. Radioligand dissociation measurements, potential interference of rebinding and allosteric mechanisms and physiological relevance of the biological model systems. Expert Opin. Drug Discov. (2012) 7 583-595.
    • (2012) Expert Opin. Drug Discov. , vol.7 , pp. 583-595
    • Vauquelin, G.1    Van Liefde, I.2
  • 20
    • 84885949138 scopus 로고    scopus 로고
    • Simplified models for heterobivalent ligand binding: when are they applicable and which are the factors that affect their target residence time
    • Vauquelin G. Simplified models for heterobivalent ligand binding: when are they applicable and which are the factors that affect their target residence time. Naunyn-Schmiedeberg's Arch. Pharmacol. (2013) 386 949-962.
    • (2013) Naunyn-Schmiedeberg's Arch. Pharmacol. , vol.386 , pp. 949-962
    • Vauquelin, G.1
  • 21
    • 79551591756 scopus 로고    scopus 로고
    • Bitopic ligands, all-in-one orthosteric and allosteric
    • Kamal M., Jockers R. Bitopic ligands, all-in-one orthosteric and allosteric. F1000 Biol. Rep. (2009) 1 77.
    • (2009) F1000 Biol. Rep. , vol.1 , pp. 77
    • Kamal, M.1    Jockers, R.2
  • 22
    • 84871806221 scopus 로고    scopus 로고
    • Bridging the gap: bitopic ligands of G-protein-coupled receptors
    • Lane J.R., Sexton P.M., Christopoulos A. Bridging the gap: bitopic ligands of G-protein-coupled receptors. Trends Pharmacol. Sci. (2013) 34 59-65.
    • (2013) Trends Pharmacol. Sci. , vol.34 , pp. 59-65
    • Lane, J.R.1    Sexton, P.M.2    Christopoulos, A.3
  • 23
    • 0020533362 scopus 로고
    • Modification of the binding properties of muscarinic receptors by gallamine
    • Stockton J.M., Birdsall N.J., Burgen A.S., Hulme E.C. Modification of the binding properties of muscarinic receptors by gallamine. Mol. Pharmacol. (1983) 23 551-557.
    • (1983) Mol. Pharmacol. , vol.23 , pp. 551-557
    • Stockton, J.M.1    Birdsall, N.J.2    Burgen, A.S.3    Hulme, E.C.4
  • 24
    • 0023958554 scopus 로고
    • Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods
    • Ehlert F.J. Estimation of the affinities of allosteric ligands using radioligand binding and pharmacological null methods. Mol. Pharmacol. (1988) 33 187-194.
    • (1988) Mol. Pharmacol. , vol.33 , pp. 187-194
    • Ehlert, F.J.1
  • 25
    • 0036258990 scopus 로고    scopus 로고
    • G protein-coupled receptor allosterism and complexing
    • Christopoulos A., Kenakin T. G protein-coupled receptor allosterism and complexing. Pharmacol. Rev. (2002) 54 323-374.
    • (2002) Pharmacol. Rev. , vol.54 , pp. 323-374
    • Christopoulos, A.1    Kenakin, T.2
  • 26
    • 0036490942 scopus 로고    scopus 로고
    • Allosteric binding sites on cell-surface receptors, novel targets for drug discovery
    • Christopoulos A. Allosteric binding sites on cell-surface receptors, novel targets for drug discovery. Nat. Rev. Drug Discov. (2002) 1 198-210.
    • (2002) Nat. Rev. Drug Discov. , vol.1 , pp. 198-210
    • Christopoulos, A.1
  • 27
    • 77955329488 scopus 로고    scopus 로고
    • Drug-target residence time: critical information for lead optimization
    • Lu H., Tonge P.J. Drug-target residence time: critical information for lead optimization. Curr. Opin. Chem. Biol. (2010) 14 467-474.
    • (2010) Curr. Opin. Chem. Biol. , vol.14 , pp. 467-474
    • Lu, H.1    Tonge, P.J.2
  • 30
    • 84862856969 scopus 로고    scopus 로고
    • Determination of drug-receptor residence times by radioligand binding and functional assays, experimental strategies and physiological relevance
    • Vauquelin G. Determination of drug-receptor residence times by radioligand binding and functional assays, experimental strategies and physiological relevance. Med. Chem. Commun. (2012) 3 645-651.
    • (2012) Med. Chem. Commun. , vol.3 , pp. 645-651
    • Vauquelin, G.1
  • 31
    • 0016749447 scopus 로고
    • Determination of dissociation constants and specific rate constants of enzyme-substrate (or protein-ligand) interactions from rapid reaction kinetic data
    • Strickland S., Palmer G., Massey V. Determination of dissociation constants and specific rate constants of enzyme-substrate (or protein-ligand) interactions from rapid reaction kinetic data. J. Biol. Chem. (1975) 250 4048-4052.
    • (1975) J. Biol. Chem. , vol.250 , pp. 4048-4052
    • Strickland, S.1    Palmer, G.2    Massey, V.3
  • 32
    • 84855840733 scopus 로고    scopus 로고
    • Target-drug interactions: first principles and their application to drug discovery
    • Núñez S., Venhorst J., Kruse C.G. Target-drug interactions: first principles and their application to drug discovery. Drug Discov. Today (2012) 17 10-22.
    • (2012) Drug Discov. Today , vol.17 , pp. 10-22
    • Núñez, S.1    Venhorst, J.2    Kruse, C.G.3
  • 33
    • 0018868014 scopus 로고
    • Opiate antagonist receptor binding in vivo: evidence for a new receptor binding model
    • Perry D.C., Mullis K.B., Øie S., Sadée W. Opiate antagonist receptor binding in vivo: evidence for a new receptor binding model. Brain Res. (1980) 199 49-61.
    • (1980) Brain Res. , vol.199 , pp. 49-61
    • Perry, D.C.1    Mullis, K.B.2    Øie, S.3    Sadée, W.4
  • 35
    • 16644394144 scopus 로고    scopus 로고
    • Effects of geometry of the immunological synapse on the delivery of effector molecules
    • Coombs D., Goldstein B. Effects of geometry of the immunological synapse on the delivery of effector molecules. Biophys. J. (2004) 87 2215-2220.
    • (2004) Biophys. J. , vol.87 , pp. 2215-2220
    • Coombs, D.1    Goldstein, B.2
  • 36
    • 77956805081 scopus 로고    scopus 로고
    • Rebinding or why drugs may act longer in vivo than expected from their in vitro target residence time
    • Vauquelin G. Rebinding or why drugs may act longer in vivo than expected from their in vitro target residence time. Expert Opin. Drug Discov. (2010) 5 927-941.
    • (2010) Expert Opin. Drug Discov. , vol.5 , pp. 927-941
    • Vauquelin, G.1
  • 37
    • 77956309074 scopus 로고    scopus 로고
    • Long-lasting target binding and rebinding as mechanisms to prolong in vivo drug action
    • Vauquelin G., Charlton S. Long-lasting target binding and rebinding as mechanisms to prolong in vivo drug action. Br. J. Pharmacol. (2010) 161 488-508.
    • (2010) Br. J. Pharmacol. , vol.161 , pp. 488-508
    • Vauquelin, G.1    Charlton, S.2
  • 38
    • 34548515751 scopus 로고    scopus 로고
    • Kinetic versus allosteric mechanisms to explain insurmountable antagonism and delayed ligand dissociation
    • Vauquelin G., Szczuka A. Kinetic versus allosteric mechanisms to explain insurmountable antagonism and delayed ligand dissociation. Neurochem. Int. (2007) 51 254-260.
    • (2007) Neurochem. Int. , vol.51 , pp. 254-260
    • Vauquelin, G.1    Szczuka, A.2
  • 39
    • 35348982265 scopus 로고    scopus 로고
    • On the benefit of bivalency in peptide ligand/Pin1 interactions
    • Daum S., Lücke C., Wildeman D., Schiener-Fischrer C. On the benefit of bivalency in peptide ligand/Pin1 interactions. J. Mol. Biol. (2007) 374 147-161.
    • (2007) J. Mol. Biol. , vol.374 , pp. 147-161
    • Daum, S.1    Lücke, C.2    Wildeman, D.3    Schiener-Fischrer, C.4
  • 40
    • 34547208823 scopus 로고    scopus 로고
    • A novel multivalent ligand that bridges the allosteric and orthosteric binding sites of the M2 muscarinic receptor
    • Steinfeld T., Mammen M., Smith J.A., Wilson R.D., Jasper J.R. A novel multivalent ligand that bridges the allosteric and orthosteric binding sites of the M2 muscarinic receptor. Mol. Pharmacol. (2007) 72 291-302.
    • (2007) Mol. Pharmacol. , vol.72 , pp. 291-302
    • Steinfeld, T.1    Mammen, M.2    Smith, J.A.3    Wilson, R.D.4    Jasper, J.R.5
  • 41
    • 77956850748 scopus 로고    scopus 로고
    • Elusive equilibrium: the challenge of interpreting receptor pharmacology using calcium assays
    • Charlton S., Vauquelin G. Elusive equilibrium: the challenge of interpreting receptor pharmacology using calcium assays. Br. J. Pharmacol. (2010) 161 1250-1265.
    • (2010) Br. J. Pharmacol. , vol.161 , pp. 1250-1265
    • Charlton, S.1    Vauquelin, G.2
  • 42
  • 43
    • 80052001378 scopus 로고    scopus 로고
    • Pathway and mechanism of drug binding to G-protein-coupled receptors
    • Dror R.O., Pana A.C., Arlowa D.H. et al. Pathway and mechanism of drug binding to G-protein-coupled receptors. Proc. Natl Acad. Sci. USA (2011) 108 13118-13123.
    • (2011) Proc. Natl Acad. Sci. USA , vol.108 , pp. 13118-13123
    • Dror, R.O.1    Pana, A.C.2    Arlowa, D.H.3
  • 44
    • 45749127879 scopus 로고    scopus 로고
    • Allosteric modulators of Class B G-protein-coupled Receptors
    • Hoare S.R.J. Allosteric modulators of Class B G-protein-coupled Receptors. Current Neuropharmacol. (2007) 5 168-179.
    • (2007) Current Neuropharmacol. , vol.5 , pp. 168-179
    • Hoare, S.R.J.1
  • 45
    • 0036839745 scopus 로고    scopus 로고
    • Dancing with different partners, protein kinase a phosphorylation of seven membrane- spanning receptors regulates their G protein-coupling specificity
    • Lefkowitz R.J., Pierce K.L., Luttrell L.M. Dancing with different partners, protein kinase a phosphorylation of seven membrane- spanning receptors regulates their G protein-coupling specificity. Mol. Pharmacol. (2002) 62 971-974.
    • (2002) Mol. Pharmacol. , vol.62 , pp. 971-974
    • Lefkowitz, R.J.1    Pierce, K.L.2    Luttrell, L.M.3
  • 46
    • 0036473397 scopus 로고    scopus 로고
    • The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals
    • Luttrell L.M., Lefkowitz R.J. The role of beta-arrestins in the termination and transduction of G-protein-coupled receptor signals. J. Cell Sci. (2002) 115 455-465.
    • (2002) J. Cell Sci. , vol.115 , pp. 455-465
    • Luttrell, L.M.1    Lefkowitz, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.