
Phage Display
A Practical Approach
Oxford University Press
Published on 4. March 2004
Book
Hardback
360 pages
978-0-19-963874-1 (ISBN)
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Description
Phage display has become established as a powerful protein engineering method for identifying polypeptides with novel properties, and altering the properties of existing ones. Although the technique is widely used in biological research and drug discovery, it remains technically challenging, and new applications and procedures continue to evolve. Phage Display- A Practical Approach is an up-to-date, comprehensive and integrated experimental guide to the technique,
useful for novice and expert alike. The book aims to enable researchers to design and undertake all aspects of a phage display project, from designing an experimental strategy and constructing a library to performing selections and analyzing the results. An introductory chapter provides an overview of
phage biology and phage display, including guidelines for planning a successful phage display experiment. Individual chapters provide protocols for constructing libraries using oligonucleotide-directed mutagenesis or DNA recombination, performing binding selections, and analyzing the binding activities of selected phage clones. Separate chapters then cover common applications, including selection of ligands from peptide libraries, generation of phage antibody libraries and isolation and
optimization of antibodies, selection of DNA binding proteins, and expression cloning using cDNA display. Further chapters describe alternative selection strategies, such as selection using immune sera, selection based on enzymatic activity or protein stability, and selection in vivo. Protocols and chapters
are extensively cross-referenced, allowing readers to move beyond the specific examples given to customize the procedures to their own protein or selection system of interest. Written by experts in the field, Phage Display- A Practical Approach provides a comprehensive guide to the design and execution of phage display projects, for all those using the technique in basic research and drug discovery.
useful for novice and expert alike. The book aims to enable researchers to design and undertake all aspects of a phage display project, from designing an experimental strategy and constructing a library to performing selections and analyzing the results. An introductory chapter provides an overview of
phage biology and phage display, including guidelines for planning a successful phage display experiment. Individual chapters provide protocols for constructing libraries using oligonucleotide-directed mutagenesis or DNA recombination, performing binding selections, and analyzing the binding activities of selected phage clones. Separate chapters then cover common applications, including selection of ligands from peptide libraries, generation of phage antibody libraries and isolation and
optimization of antibodies, selection of DNA binding proteins, and expression cloning using cDNA display. Further chapters describe alternative selection strategies, such as selection using immune sera, selection based on enzymatic activity or protein stability, and selection in vivo. Protocols and chapters
are extensively cross-referenced, allowing readers to move beyond the specific examples given to customize the procedures to their own protein or selection system of interest. Written by experts in the field, Phage Display- A Practical Approach provides a comprehensive guide to the design and execution of phage display projects, for all those using the technique in basic research and drug discovery.
Reviews / Votes
...this is a nicely presented, readable text in which most people who use the technique in the laboratory will be able to find something useful. Richard J. Reece, University of Manchester.More details
Language
English
Place of publication
Oxford
United Kingdom
Target group
Professional and scholarly
Illustrations
48 Line figures, 1 halftone and 14 Tables
Dimensions
Height: 253 mm
Width: 194 mm
Thickness: 25 mm
Weight
957 gr
ISBN-13
978-0-19-963874-1 (9780199638741)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

Book
02/2004
Oxford University Press
€100.28
Shipment within 15-20 days
Persons
Dr Tim Clackson
Vice President, Gene Therapy and Genomics
ARIAD Pharmaceuticals, Inc., 26 Landsdowne Street, Cambridge, MA 02139, USA
+1 617 494 0400 ext. 258
+1 617 225 2589
clackson@ariad.com
Tim Clackson, Ph.D. is Senior Vice President, Science and Technology at ARIAD Pharmaceuticals, Inc., where he has served for eight years in a variety of research and research management positions. His group is combining chemistry, cell biology and protein engineering to develop techniques for regulating gene expression and other intracellular processes using small molecules. Dr Clackson's particular research interest is the use of protein engineering and chemical biology techniques to analyze
and redesign the interfaces between molecules, especially small molecule-protein interfaces.
Dr Henry B. Lowman
Senior Scientist
Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA
+1 650 225 1171
+1 650 225 3734
hbl@gene.com
Henry B. Lowman, Ph.D. is a Senior Scientist and Associate Director of Antibody Engineering with joint appointments in Immunology and Protein Engineering, at Genentech, Inc., where he has been engaged in research on proteins and peptides for over thirteen years.
Vice President, Gene Therapy and Genomics
ARIAD Pharmaceuticals, Inc., 26 Landsdowne Street, Cambridge, MA 02139, USA
+1 617 494 0400 ext. 258
+1 617 225 2589
clackson@ariad.com
Tim Clackson, Ph.D. is Senior Vice President, Science and Technology at ARIAD Pharmaceuticals, Inc., where he has served for eight years in a variety of research and research management positions. His group is combining chemistry, cell biology and protein engineering to develop techniques for regulating gene expression and other intracellular processes using small molecules. Dr Clackson's particular research interest is the use of protein engineering and chemical biology techniques to analyze
and redesign the interfaces between molecules, especially small molecule-protein interfaces.
Dr Henry B. Lowman
Senior Scientist
Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA
+1 650 225 1171
+1 650 225 3734
hbl@gene.com
Henry B. Lowman, Ph.D. is a Senior Scientist and Associate Director of Antibody Engineering with joint appointments in Immunology and Protein Engineering, at Genentech, Inc., where he has been engaged in research on proteins and peptides for over thirteen years.
Content
1. Introduction to phage biology and phage display ; 2. Constructing phage display libraries by oligonucleotide-directed mutagenesis ; 3. In vitro DNA recombination ; 4. Phage selection strategies for improved affinity and specificity of proteins and peptides ; 5. Rapid screening of phage displayed protein binding affinities by phage ELISA ; 6. Identification of novel ligands for receptors using recombinant peptide libraries ; 7. Substrate phage display ; 8. Protease-based selection of stably folded proteins and protein domains from phage display libraries ; 9. Phage display of zinc fingers and other nucleic acid-binding motifs ; 10. In vivo and ex vivo selections using phage-displayed libraries ; 11. Screening phage libraries with sera ; 12. Interaction cloning using cDNA libraries displayed on phage ; 13. Phage antibody libraries ; 14. Affinity maturation of phage antibodies