Bacterial display in combinatorial protein engineering

被引:85
作者
Lofblom, John [1 ]
机构
[1] AlbaNova Univ Ctr, Div Mol Biotechnol, Sch Biotechnol, Royal Inst Technol KTH, SE-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Bacterial display; Biopharmaceuticals; Combinatorial protein engineering; Phage display; Recombinant antibodies; CELL-SURFACE DISPLAY; ANCHORED PERIPLASMIC EXPRESSION; FRAGMENT COMPLEMENTATION ASSAY; FINE AFFINITY DISCRIMINATION; LENGTH IGG ANTIBODIES; STAPHYLOCOCCUS-CARNOSUS; ESCHERICHIA-COLI; AFFIBODY MOLECULES; PEPTIDE LIGANDS; FLOW-CYTOMETRY;
D O I
10.1002/biot.201100129
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Technologies for display of recombinant protein libraries are today essential tools in many research-intensive fields, such as in the drug discovery processes of biopharmaceutical development. Phage display is still the most widely used method, but alternative systems are available and are becoming increasingly popular. The most rapidly expanding of the alternative systems are the cell display-based technologies, offering innovative strategies for selection and characterization of affinity proteins. Most investigations have focused on eukaryotic yeast for display of protein libraries, but similar systems are also being developed using prokaryotic hosts. This review summarizes the field of bacterial surface display with a strong emphasis on library applications for generation of new affinity proteins. The main focus will be on the most recent progress of the work on primarily Escherichia coli, but also on studies using a recently developed system for display on Gram-positive Staphylococcus carnosus. In addition, general strategies for combinatorial protein engineering using cell display are discussed along with the latest developments of new methodologies with comparisons to mainly phage display technology.
引用
收藏
页码:1115 / 1129
页数:15
相关论文
共 99 条
[1]   Radionuclide Molecular Imaging Using Affibody Molecules [J].
Ahlgren, Sara ;
Tolmachev, Vladimir .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2010, 11 (06) :581-589
[2]   A small bispecific protein selected for orthogonal affinity purification [J].
Alm, Tove ;
Yderland, Louise ;
Nilvebrant, Johan ;
Halldin, Anneli ;
Hober, Sophia .
BIOTECHNOLOGY JOURNAL, 2010, 5 (06) :605-617
[3]   Extending Half-life by Indirect Targeting of the Neonatal Fc Receptor (FcRn) Using a Minimal Albumin Binding Domain [J].
Andersen, Jan Terje ;
Pehrson, Rikard ;
Tolmachev, Vladimir ;
Daba, Muluneh Bekele ;
Abrahmsen, Lars ;
Ekblad, Caroline .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (07) :5234-5241
[4]  
Andreoni C, 1997, BIOTECHNIQUES, V23, P696
[5]   Isolation of human monoclonal antibodies by mammalian cell display [J].
Beerli, Roger R. ;
Bauer, Monika ;
Buser, Regula B. ;
Gwerder, Myriam ;
Muntwiler, Simone ;
Maurer, Patrik ;
Saudan, Philippe ;
Bachmann, Martin F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (38) :14336-14341
[6]   Rapid isolation of high-affinity protein binding peptides using bacterial display [J].
Bessette, PH ;
Rice, JJ ;
Daugherty, PS .
PROTEIN ENGINEERING DESIGN & SELECTION, 2004, 17 (10) :731-739
[7]   High-throughput Sorting of an Anticalin Library via EspP-mediated Functional Display on the Escherichia coli Cell Surface [J].
Binder, Uli ;
Matschiner, Gabriele ;
Theobald, Ina ;
Skerra, Arne .
JOURNAL OF MOLECULAR BIOLOGY, 2010, 400 (04) :783-802
[8]   Evolving strategies for enzyme engineering [J].
Bloom, JD ;
Meyer, MM ;
Meinhold, P ;
Otey, CR ;
MacMillan, D ;
Arnold, FH .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2005, 15 (04) :447-452
[9]   Yeast surface display for screening combinatorial polypeptide libraries [J].
Boder, ET ;
Wittrup, KD .
NATURE BIOTECHNOLOGY, 1997, 15 (06) :553-557
[10]   Antigen selection from an HIV-1 immune antibody library displayed on yeast yields many novel antibodies compared to selection from the same library displayed on phage [J].
Bowley, D. R. ;
Labrijn, A. F. ;
Zwick, M. B. ;
Burton, D. R. .
PROTEIN ENGINEERING DESIGN & SELECTION, 2007, 20 (02) :81-90