Citation: | DAI He-ping, GAO Hong, ZHAO Xin-yan. PHAGE DISPLAY TECHNOLOGY PRINCIPLE AND METHODS[J]. ACTA HYDROBIOLOGICA SINICA, 2002, 26(4): 400-409. |
[1] |
Smith G P.Filamentous Fusion phage:novel expression vector that display cloned antigens on the viron surface [J].Science,1985,228:1315-1317[2] Scott J K,Smith G P.Searching for peptide ligands with an epitope library [J].Science.1990,246:386-390[3] McCafferty J,Griffiths A D,Winter G,et al.Phage antibodies:filamentous phage displaying antibody variable domains[J].Nature.1990,348:552-554[4] 许正平和李伯良.噬菌体展示系统的研究进展[J].生命的化学,1996,16:29-34[5] Efimov V P.Bacteriophage T4 as a surface display vector[J].Virus Genes.1995,10:173-177[6] Mottershead D,Vander Linden I,Bonsdroff C-H,et al.Baculoviral display of the green fluorescent protein and rubella virus envelop proteins[J].Biochem Biophys Res.Commun.1997,238:717-722[7] Rose C,Andrews W,Ferguson M,et al.The construction and characterization of poliovirus antigen chimeras presenting defined regions of the human T 1ymphocyte marker CD4[J].J.Gen.Virol.1994,75(Pt 5):969-977[8] Resnick D A,Smith A D,Geisler S C,et al.Chimeras from a human rhinovirus 14-human immuno-deficiency virus type 1(HIV-1)V3 1oop seroprevalence library induce neutralizing responses against HIV-1[J].J.Virol.1995, 69:2406-11[9] Ohno K,Sawai K,Li jima Y,et al.Cell-specific targeting of sindbis virus vectors displaying IgG-binding domains of protein A[J].Nat.Biotechnol.1997,15:763-767[10] Kayman S C,Park H,Saxon M,et al.The hypervariable domain of the murine leukemia virus surface protein tolerates large insertions and deletions,enabling development of a retroviral particle display system[J].J.Virol.1999,73:1802-1808[11] Porta C,Spall V E,Loveland J,et al.Development of cowpea mosaic virus as a high-yielding system for the presentation of foreign peptides[J].Virology.1994,202:949-955[12] Turpen T H,Reinl S J,Charonenvit Y,et al.Malarial epitopes expressed on the surface of recombinant tobacco mosaic virus[J].Bio.technology.1995,13:53-57[13] Francisco J A,Campbell R,Iverson B L et al.Production and fluorescence-activated cell sorting of Escherichia coli expressing a functional antibody fragrant on the external surface[J].Proc.Natl.Acad.Sci.USA.1993,99:10444-10448[14] Boder E T,Wittrup K D.Yeast surface display for screening combinatorial polypeptide libraries[J].Nat.Biotechnol.1997, 15:553-557[15] Fitzgerald K.In vitro display technologies-new tools for drug discovery [J].Drug.Discov.Today.2000,5:253-258[16] Liu Y,Haggard-Lungquist E.Studies of bacteriophage P2 DNA replication:Localization of the cleavage site of the A protein[J].Nucleic Acids Res.1994,22:5204-5210[17] Schaffitzel C,Liu Y.Ribosome display:in vitro method for selection and evolution of antibodies from libraries[J].J.Immunol.Methods.1999,231:119-135[18] Roberts R W,Szostak J W.RNA-peptide fusion for the in vitro selection of peptides and proteins[J].Proc.Natl.Acad.Sci.USA.1997,94:12297-12302[19] Schier R,Balint R F,Mccall A,et al.Identification of functional and structural amino-acid residues by parsimonious mutagenesis[J].Gene[J].1996,169:147-155[20] Glasser S M,Yelton D E,Huse W D.Antibody engineering by codon-based mutagenesis in a filamentous phage system[J].J.Immunol[J].1992,149:3903-3913[21] Virnekas B,Gre L,Pluckthun A,et al.Trinucleotides for random mutagenesis:ideal reagents for the synthesis of mixed oligonucleotides for random mutagenesis[J].Nucleic Acids Res.1994,22:5600-5607[22] Iannolo G,Minenkova O,Gonfloni S,et al.construction,exploitation and evolution of a new peptide library displayed at high density by fusion to major coat protein of filamentous phage[J].Biol.Chem.1997,378:517-521[23] Brown K C.New approaches for cell-specific targeting:identification of cell-selective peptides from combinatiorial libraries[J].Current Opin.Chem.Biol.2000,4:16-21[24] Szardenings M,Tormroth S,Mutulis F,et al.Phage display selection on whole cells yields a peptide specific for melanocortin receptor[J].J.Biol.Chem.1997,272:27943-27948[25] Doorbar J,Winter G.Isolation of a peptide antagonist to the thrombin receptor using phage display[J].J.Mol.Bio.1994,244:361-369[26] Barry M A,Dower E J,Johnston S A.Toward cell-targeting gene therapy vector:selection of cell-binding peptides from random peptide presenting phage libraries[J].Nat.Med [J].1996,2:299-305[27] Mazzucchelli L,Burrit J B,Jesaitis A J,et al.cell-specific peptide binding by human neutrophils [J].Blood.1999,93:1738-1748[28] Ivanenkov V,V,felice F,Menon A G.Uptakes and intracellular fate of phage display vectors into mammalian cells[J].Biochem Biophys.Acta.1999,1448:450-462[29] Ivanenkov V V,felice F,Menon A G.targeted delivery of multivalent phage display vectors into mammalian cells[J].Biochem Biophys.Acta.1999,1448:463-472.[30] Pasqualini R,Ruoslahti E.Organ targeting in vivo using phage display peptide libraries[J].Nature.1996,380:364-366[31] Rajott D,Arap W,Hagerdorn M,et al.molecular heterogeneity of the vascular endothelium revealed by in vivo phage display[J].J.clinc Invest.1998,102:430-437[32] Arap W,Pasqualini R,Ruoslahti E.Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model[J].Science.1998,279:377-380[33] Larocca D,Witte A,Johnson W,et al.Targeting bacteriophage to mammalian cell surface receptors for gene delivery[J].Hum.Gene Ther.1998,9:2393-2399[34] Bartoli F,Nuzzo M,Urbanelli L,et al.DNA-based selection and screening of peptide ligands[J].Nat.Biotechnol.1998,16:1068-1073[35] Pedrazzi G,Schwesinger F,Honegger A,et al.Affinity and folding properties both influence the selection of antibodies with the selectively infective phage(SIP)methodology[J].FEBS letters.1997,415:289-293
Smith G P.Filamentous Fusion phage:novel expression vector that display cloned antigens on the viron surface [J].Science,1985,228:1315-1317[2] Scott J K,Smith G P.Searching for peptide ligands with an epitope library [J].Science.1990,246:386-390[3] McCafferty J,Griffiths A D,Winter G,et al.Phage antibodies:filamentous phage displaying antibody variable domains[J].Nature.1990,348:552-554[4] 许正平和李伯良.噬菌体展示系统的研究进展[J].生命的化学,1996,16:29-34[5] Efimov V P.Bacteriophage T4 as a surface display vector[J].Virus Genes.1995,10:173-177[6] Mottershead D,Vander Linden I,Bonsdroff C-H,et al.Baculoviral display of the green fluorescent protein and rubella virus envelop proteins[J].Biochem Biophys Res.Commun.1997,238:717-722[7] Rose C,Andrews W,Ferguson M,et al.The construction and characterization of poliovirus antigen chimeras presenting defined regions of the human T 1ymphocyte marker CD4[J].J.Gen.Virol.1994,75(Pt 5):969-977[8] Resnick D A,Smith A D,Geisler S C,et al.Chimeras from a human rhinovirus 14-human immuno-deficiency virus type 1(HIV-1)V3 1oop seroprevalence library induce neutralizing responses against HIV-1[J].J.Virol.1995, 69:2406-11[9] Ohno K,Sawai K,Li jima Y,et al.Cell-specific targeting of sindbis virus vectors displaying IgG-binding domains of protein A[J].Nat.Biotechnol.1997,15:763-767[10] Kayman S C,Park H,Saxon M,et al.The hypervariable domain of the murine leukemia virus surface protein tolerates large insertions and deletions,enabling development of a retroviral particle display system[J].J.Virol.1999,73:1802-1808[11] Porta C,Spall V E,Loveland J,et al.Development of cowpea mosaic virus as a high-yielding system for the presentation of foreign peptides[J].Virology.1994,202:949-955[12] Turpen T H,Reinl S J,Charonenvit Y,et al.Malarial epitopes expressed on the surface of recombinant tobacco mosaic virus[J].Bio.technology.1995,13:53-57[13] Francisco J A,Campbell R,Iverson B L et al.Production and fluorescence-activated cell sorting of Escherichia coli expressing a functional antibody fragrant on the external surface[J].Proc.Natl.Acad.Sci.USA.1993,99:10444-10448[14] Boder E T,Wittrup K D.Yeast surface display for screening combinatorial polypeptide libraries[J].Nat.Biotechnol.1997, 15:553-557[15] Fitzgerald K.In vitro display technologies-new tools for drug discovery [J].Drug.Discov.Today.2000,5:253-258[16] Liu Y,Haggard-Lungquist E.Studies of bacteriophage P2 DNA replication:Localization of the cleavage site of the A protein[J].Nucleic Acids Res.1994,22:5204-5210[17] Schaffitzel C,Liu Y.Ribosome display:in vitro method for selection and evolution of antibodies from libraries[J].J.Immunol.Methods.1999,231:119-135[18] Roberts R W,Szostak J W.RNA-peptide fusion for the in vitro selection of peptides and proteins[J].Proc.Natl.Acad.Sci.USA.1997,94:12297-12302[19] Schier R,Balint R F,Mccall A,et al.Identification of functional and structural amino-acid residues by parsimonious mutagenesis[J].Gene[J].1996,169:147-155[20] Glasser S M,Yelton D E,Huse W D.Antibody engineering by codon-based mutagenesis in a filamentous phage system[J].J.Immunol[J].1992,149:3903-3913[21] Virnekas B,Gre L,Pluckthun A,et al.Trinucleotides for random mutagenesis:ideal reagents for the synthesis of mixed oligonucleotides for random mutagenesis[J].Nucleic Acids Res.1994,22:5600-5607[22] Iannolo G,Minenkova O,Gonfloni S,et al.construction,exploitation and evolution of a new peptide library displayed at high density by fusion to major coat protein of filamentous phage[J].Biol.Chem.1997,378:517-521[23] Brown K C.New approaches for cell-specific targeting:identification of cell-selective peptides from combinatiorial libraries[J].Current Opin.Chem.Biol.2000,4:16-21[24] Szardenings M,Tormroth S,Mutulis F,et al.Phage display selection on whole cells yields a peptide specific for melanocortin receptor[J].J.Biol.Chem.1997,272:27943-27948[25] Doorbar J,Winter G.Isolation of a peptide antagonist to the thrombin receptor using phage display[J].J.Mol.Bio.1994,244:361-369[26] Barry M A,Dower E J,Johnston S A.Toward cell-targeting gene therapy vector:selection of cell-binding peptides from random peptide presenting phage libraries[J].Nat.Med [J].1996,2:299-305[27] Mazzucchelli L,Burrit J B,Jesaitis A J,et al.cell-specific peptide binding by human neutrophils [J].Blood.1999,93:1738-1748[28] Ivanenkov V,V,felice F,Menon A G.Uptakes and intracellular fate of phage display vectors into mammalian cells[J].Biochem Biophys.Acta.1999,1448:450-462[29] Ivanenkov V V,felice F,Menon A G.targeted delivery of multivalent phage display vectors into mammalian cells[J].Biochem Biophys.Acta.1999,1448:463-472.[30] Pasqualini R,Ruoslahti E.Organ targeting in vivo using phage display peptide libraries[J].Nature.1996,380:364-366[31] Rajott D,Arap W,Hagerdorn M,et al.molecular heterogeneity of the vascular endothelium revealed by in vivo phage display[J].J.clinc Invest.1998,102:430-437[32] Arap W,Pasqualini R,Ruoslahti E.Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model[J].Science.1998,279:377-380[33] Larocca D,Witte A,Johnson W,et al.Targeting bacteriophage to mammalian cell surface receptors for gene delivery[J].Hum.Gene Ther.1998,9:2393-2399[34] Bartoli F,Nuzzo M,Urbanelli L,et al.DNA-based selection and screening of peptide ligands[J].Nat.Biotechnol.1998,16:1068-1073[35] Pedrazzi G,Schwesinger F,Honegger A,et al.Affinity and folding properties both influence the selection of antibodies with the selectively infective phage(SIP)methodology[J].FEBS letters.1997,415:289-293
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