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Volumn 33, Issue 5, 2012, Pages 261-267

Rapid-access, high-throughput synchrotron crystallography for drug discovery

Author keywords

[No Author keywords available]

Indexed keywords

BETA SECRETASE; MEMBRANE PROTEIN;

EID: 84860527565     PISSN: 01656147     EISSN: 18733735     Source Type: Journal    
DOI: 10.1016/j.tips.2012.03.009     Document Type: Review
Times cited : (24)

References (40)
  • 1
    • 73449101512 scopus 로고    scopus 로고
    • Lessons from 60 years of pharmaceutical innovation
    • B. Munos Lessons from 60 years of pharmaceutical innovation Nat. Rev. Drug Discov. 8 2009 959 968
    • (2009) Nat. Rev. Drug Discov. , vol.8 , pp. 959-968
    • Munos, B.1
  • 2
    • 4344645978 scopus 로고    scopus 로고
    • Can the pharmaceutical industry reduce attrition rates?
    • I. Kola, and J. Landis Can the pharmaceutical industry reduce attrition rates? Nat. Rev. Drug Discov. 3 2004 711 715 (Pubitemid 39173511)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.8 , pp. 711-715
    • Kola, I.1    Landis, J.2
  • 3
    • 0036051992 scopus 로고    scopus 로고
    • High-throughput crystallography for lead discovery in drug design
    • T.L. Blundell High-throughput crystallography for lead discovery in drug design Nat. Rev. Drug Discov. 1 2002 45 54 (Pubitemid 37361403)
    • (2002) Nature Reviews Drug Discovery , vol.1 , Issue.1 , pp. 45-54
    • Blundell, T.L.1    Jhoti, H.2    Abell, C.3
  • 4
    • 21544474149 scopus 로고    scopus 로고
    • Structural biology and drug discovery
    • M. Congreve Structural biology and drug discovery Drug Discov. Today 10 2005 895 907
    • (2005) Drug Discov. Today , vol.10 , pp. 895-907
    • Congreve, M.1
  • 5
    • 33745161050 scopus 로고    scopus 로고
    • Structural biology and drug discovery
    • DOI 10.2174/138161206777585201
    • G. Scapin Structural biology and drug discovery Curr. Pharm. Des. 12 2006 2087 2097 (Pubitemid 43891405)
    • (2006) Current Pharmaceutical Design , vol.12 , Issue.17 , pp. 2087-2097
    • Scapin, G.1
  • 6
    • 84920752523 scopus 로고    scopus 로고
    • High-throughput crystallographic data collection at synchrotrons
    • M.R. Sanderson, J.V. Skelly, Oxford University Press
    • S.R. Wasserman High-throughput crystallographic data collection at synchrotrons M.R. Sanderson, J.V. Skelly, Macromolecular Crystallography: Conventional and High-Throughput Methods 2007 Oxford University Press 173 189
    • (2007) Macromolecular Crystallography: Conventional and High-Throughput Methods , pp. 173-189
    • Wasserman, S.R.1
  • 7
    • 0023444273 scopus 로고
    • Synchrotron radiation
    • H. Winick Synchrotron radiation Sci. Am. 257 1987 88 99
    • (1987) Sci. Am. , vol.257 , pp. 88-99
    • Winick, H.1
  • 9
    • 70349901077 scopus 로고    scopus 로고
    • High-throughput crystallography for structural genomics
    • A. Joachimiak High-throughput crystallography for structural genomics Curr. Opin. Struct. Biol. 19 2009 573 584
    • (2009) Curr. Opin. Struct. Biol. , vol.19 , pp. 573-584
    • Joachimiak, A.1
  • 10
    • 0026095584 scopus 로고
    • Determination of macromolecular structures from anomalous diffraction of synchrotron radiation
    • W.A. Hendrickson Determination of macromolecular structures from anomalous diffraction of synchrotron radiation Science 254 1991 51 58 (Pubitemid 21917315)
    • (1991) Science , vol.254 , Issue.5028 , pp. 51-58
    • Hendrickson, W.A.1
  • 11
  • 12
    • 33750565735 scopus 로고    scopus 로고
    • Biomolecular interaction analysis in drug discovery using surface plasmon resonance technology
    • DOI 10.2174/138161206778743600
    • W. Huber, and F. Mueller Biomolecular interaction analysis in drug discovery using surface plasmon resonance technology Curr. Pharm. Des. 12 2006 3999 4021 (Pubitemid 44669759)
    • (2006) Current Pharmaceutical Design , vol.12 , Issue.31 , pp. 3999-4021
    • Huber, W.1    Mueller, F.2
  • 13
    • 3142549812 scopus 로고    scopus 로고
    • CATS: A cryogenic automated transfer system installed on the beamline FIP at ESRF
    • J. Ohana CATS: a cryogenic automated transfer system installed on the beamline FIP at ESRF J. Appl. Crystallogr. 37 2004 72 77
    • (2004) J. Appl. Crystallogr. , vol.37 , pp. 72-77
    • Ohana, J.1
  • 19
    • 0031059866 scopus 로고    scopus 로고
    • Processing of X-ray diffraction data collected in oscillation mode
    • DOI 10.1016/S0076-6879(97)76066-X
    • Otwinowski, Z. and Minor, W. (1997) Processing of X-ray diffraction data collected in oscillation mode. In Methods in Enzymology. vol. 276. Macromolecular Crystallography, Part A (Carter, C.W., Jr and Sweet, R.M., eds), pp. 307-326, Academic Press (Pubitemid 27085611)
    • (1997) Methods in Enzymology , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2
  • 20
    • 12344313512 scopus 로고    scopus 로고
    • High throughput crystallography on an in-house source, using Actor
    • A.J. Sharff High throughput crystallography on an in-house source, using Actor Rigaku J. 19-20 2003 5 10
    • (2003) Rigaku J. , vol.19-20 , pp. 5-10
    • Sharff, A.J.1
  • 21
    • 15944394229 scopus 로고    scopus 로고
    • High-throughput X-ray crystallography for drug discovery
    • DOI 10.1016/j.coph.2004.04.007, PII S1471489204001225
    • T.L. Blundell, and S. Patel High-throughput X-ray crystallography for drug discovery Curr. Opin. Pharmacol. 4 2004 490 496 (Pubitemid 40533010)
    • (2004) Current Opinion in Pharmacology , vol.4 , Issue.5 , pp. 490-496
    • Blundell, T.L.1    Patel, S.2
  • 22
    • 84864878309 scopus 로고    scopus 로고
    • Fragment-based lead discovery and optimization using x-ray crystallography, computational chemistry and high-throughput organic synthesis
    • W. Jahnke, D.A. Erlanson, Wiley-VCH Verlag
    • J. Blaney Fragment-based lead discovery and optimization using x-ray crystallography, computational chemistry and high-throughput organic synthesis W. Jahnke, D.A. Erlanson, Fragment-based Approaches in Drug Discovery 2006 Wiley-VCH Verlag 215 248
    • (2006) Fragment-based Approaches in Drug Discovery , pp. 215-248
    • Blaney, J.1
  • 23
    • 73649110303 scopus 로고    scopus 로고
    • Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: The NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ
    • J.E. Brownell Substrate-assisted inhibition of ubiquitin-like protein-activating enzymes: the NEDD8 E1 inhibitor MLN4924 forms a NEDD8-AMP mimetic in situ Mol. Cell 37 2010 102 111
    • (2010) Mol. Cell , vol.37 , pp. 102-111
    • Brownell, J.E.1
  • 24
    • 80051991015 scopus 로고    scopus 로고
    • Structure of the protein core of the glypican Dally-like and localization of a region important for hedgehog signaling
    • M.-S. Kim Structure of the protein core of the glypican Dally-like and localization of a region important for hedgehog signaling Proc. Natl. Acad. Sci. U.S.A. 108 2011 13112 13117
    • (2011) Proc. Natl. Acad. Sci. U.S.A. , vol.108 , pp. 13112-13117
    • Kim, M.-S.1
  • 25
    • 81555204380 scopus 로고    scopus 로고
    • Structural basis of RNA recognition and activation by innate immune receptor RIG-I
    • F. Jiang Structural basis of RNA recognition and activation by innate immune receptor RIG-I Nature 479 2011 423 427
    • (2011) Nature , vol.479 , pp. 423-427
    • Jiang, F.1
  • 26
    • 77249095150 scopus 로고    scopus 로고
    • Structures of human Bruton's tyrosine kinase in active and inactive conformations suggest a mechanism of activation for TEC family kinases
    • D.J. Marcotte Structures of human Bruton's tyrosine kinase in active and inactive conformations suggest a mechanism of activation for TEC family kinases Protein Sci. 19 2010 429 439
    • (2010) Protein Sci. , vol.19 , pp. 429-439
    • Marcotte, D.J.1
  • 27
    • 80053615320 scopus 로고    scopus 로고
    • The significance of G protein-coupled receptor crystallography for drug discovery
    • J.A. Salon The significance of G protein-coupled receptor crystallography for drug discovery Pharmacol. Rev. 63 2011 901 937
    • (2011) Pharmacol. Rev. , vol.63 , pp. 901-937
    • Salon, J.A.1
  • 28
    • 20644436026 scopus 로고    scopus 로고
    • Will reduced radiation damage occur with very small crystals?
    • DOI 10.1107/S0909049505003274
    • C. Nave, and M.A. Hill Will reduced radiation damage occur with very small crystals? J. Synchrotron Radiat. 12 2005 299 303 (Pubitemid 41557607)
    • (2005) Journal of Synchrotron Radiation , vol.12 , Issue.3 , pp. 299-303
    • Nave, C.1    Hill, M.A.2
  • 29
    • 61449217095 scopus 로고    scopus 로고
    • Mini-beam collimator enables microcrystallography experiments on standard beamlines
    • R.F. Fischetti Mini-beam collimator enables microcrystallography experiments on standard beamlines J. Synchrotron Radiat. 16 2009 217 225
    • (2009) J. Synchrotron Radiat. , vol.16 , pp. 217-225
    • Fischetti, R.F.1
  • 32
    • 77955043039 scopus 로고    scopus 로고
    • New microbeam beamline at SPring-8, targeting at protein micro-crystallography
    • K. Hirata New microbeam beamline at SPring-8, targeting at protein micro-crystallography AIP Conf. Proc. 1234 2010 901 904
    • (2010) AIP Conf. Proc. , vol.1234 , pp. 901-904
    • Hirata, K.1
  • 33
    • 66049128793 scopus 로고    scopus 로고
    • Crystallizing membrane proteins for structure determination: Use of lipidic mesophases
    • M. Caffrey Crystallizing membrane proteins for structure determination: use of lipidic mesophases Annu. Rev. Biophys. 38 2009 29 51
    • (2009) Annu. Rev. Biophys. , vol.38 , pp. 29-51
    • Caffrey, M.1
  • 34
    • 69949132434 scopus 로고    scopus 로고
    • Rastering strategy for screening and centring of microcrystal samples of human membrane proteins with a sub-10 μm size X-ray synchrotron beam
    • V. Cherezov Rastering strategy for screening and centring of microcrystal samples of human membrane proteins with a sub-10 μm size X-ray synchrotron beam J. R. Soc. Interface 6 2009 S587 S597
    • (2009) J. R. Soc. Interface , vol.6
    • Cherezov, V.1
  • 35
    • 79959518091 scopus 로고    scopus 로고
    • Second-order nonlinear optical imaging of chiral crystals
    • D.J. Kissick Second-order nonlinear optical imaging of chiral crystals Annu. Rev. Anal. Chem. 4 2011 419 437
    • (2011) Annu. Rev. Anal. Chem. , vol.4 , pp. 419-437
    • Kissick, D.J.1
  • 38
    • 65749117953 scopus 로고    scopus 로고
    • Synchrotron applications of pixel and strip detectors at Diamond Light Source
    • J. Marchal Synchrotron applications of pixel and strip detectors at Diamond Light Source Nucl. Instrum. Methods Phys. Res. A 604 2009 123 126
    • (2009) Nucl. Instrum. Methods Phys. Res. A , vol.604 , pp. 123-126
    • Marchal, J.1
  • 39
    • 0001704894 scopus 로고
    • Oscillation photography of radiation-sensitive crystals using a synchrotron source
    • M.G. Rossman, and J.W. Erickson Oscillation photography of radiation-sensitive crystals using a synchrotron source J. Appl. Crystallogr. 16 1983 629 636
    • (1983) J. Appl. Crystallogr. , vol.16 , pp. 629-636
    • Rossman, M.G.1    Erickson, J.W.2
  • 40
    • 81255143061 scopus 로고    scopus 로고
    • Robust central reduction of amyloid-β in humans with an orally available, non-peptidic β-secretase inhibitor
    • P.C. May Robust central reduction of amyloid-β in humans with an orally available, non-peptidic β-secretase inhibitor J. Neurosci. 16 2011 16507 16516
    • (2011) J. Neurosci. , vol.16 , pp. 16507-16516
    • May, P.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.