Design and Screening of M13 Phage Display cDNA Libraries

被引:34
|
作者
Georgieva, Yuliya [1 ,2 ]
Konthur, Zoltan [1 ]
机构
[1] Max Planck Inst Mol Genet, Dept Vertebrate Genom, D-14195 Berlin, Germany
[2] Free Univ Berlin, Dept Biol Chem & Pharm, D-14195 Berlin, Germany
关键词
phage display; cDNA library; ORF selection; phagemid; protein-protein interaction; next generation sequencing (NGS); OPEN READING FRAMES; ANTIBODY VARIABLE DOMAINS; FD ADSORPTION PROTEIN; FILAMENTOUS PHAGE; ESCHERICHIA-COLI; SURFACE EXPRESSION; FUNCTIONAL CLONING; BACTERIOPHAGE FD; HELPER PHAGE; SELECTION;
D O I
10.3390/molecules16021667
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The last decade has seen a steady increase in screening of cDNA expression product libraries displayed on the surface of filamentous bacteriophage. At the same time, the range of applications extended from the identification of novel allergens over disease markers to protein-protein interaction studies. However, the generation and selection of cDNA phage display libraries is subjected to intrinsic biological limitations due to their complex nature and heterogeneity, as well as technical difficulties regarding protein presentation on the phage surface. Here, we review the latest developments in this field, discuss a number of strategies and improvements anticipated to overcome these challenges making cDNA and open reading frame (ORF) libraries more readily accessible for phage display. Furthermore, future trends combining phage display with next generation sequencing (NGS) will be presented.
引用
收藏
页码:1667 / 1681
页数:15
相关论文
共 50 条
  • [1] Selection of peptides binding to metallic borides by screening M13 phage display libraries
    Ploss, Martin
    Facey, Sandra J.
    Bruhn, Carina
    Zemel, Limor
    Hofmann, Kathrin
    Stark, Robert W.
    Albert, Barbara
    Hauer, Bernhard
    BMC BIOTECHNOLOGY, 2014, 14
  • [2] Selection of peptides binding to metallic borides by screening M13 phage display libraries
    Martin Ploss
    Sandra J Facey
    Carina Bruhn
    Limor Zemel
    Kathrin Hofmann
    Robert W Stark
    Barbara Albert
    Bernhard Hauer
    BMC Biotechnology, 14
  • [3] Design and screening of M13 phage libraries directed against beta amyloid.
    Orner, BP
    Kiessling, LL
    Murphy, RM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 225 : U212 - U213
  • [4] Engineering M13 for phage display
    Sidhu, SS
    BIOMOLECULAR ENGINEERING, 2001, 18 (02): : 57 - 63
  • [5] COMPARISON OF PLATE VERSUS LIQUID AMPLIFICATION OF M13 PHAGE DISPLAY LIBRARIES
    MCCONNELL, SJ
    UVEGES, AJ
    SPINELLA, DG
    BIOTECHNIQUES, 1995, 18 (05) : 803 - &
  • [6] Construction and screening of M13 phage libraries displaying long random peptides
    McConnell, SJ
    Uveges, AJ
    Fowlkes, DM
    Spinella, DG
    MOLECULAR DIVERSITY, 1996, 1 (03) : 165 - 176
  • [7] Construction and screening of M13 phage-displayed random peptide libraries
    Adey, NB
    Guo, R
    Hanson, HL
    Rider, JE
    Sparks, AB
    Kay, BK
    METHODS IN MOLECULAR AND CELLULAR BIOLOGY, 1996, 6 (01): : 34 - 45
  • [8] Oligopeptide M13 Phage Display in Pathogen Research
    Kuegler, Jonas
    Zantow, Jonas
    Meyer, Torsten
    Hust, Michael
    VIRUSES-BASEL, 2013, 5 (10): : 2531 - 2545
  • [9] Modulation of antibody display on M13 filamentous phage
    Chappel, JA
    He, M
    Kang, AS
    JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 221 (1-2) : 25 - 34
  • [10] Phage survival: The biodegradability of M13 phage display library in vitro
    Tothova, L'ubomira
    Babickova, Janka
    Celec, Peter
    BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2012, 59 (06) : 490 - 494