Chapter title |
Identifying Bacterial Immune Evasion Proteins Using Phage Display.
|
---|---|
Chapter number | 4 |
Book title |
Bacterial Pathogenesis
|
Published in |
Methods in molecular biology, January 2017
|
DOI | 10.1007/978-1-4939-6673-8_4 |
Pubmed ID | |
Book ISBNs |
978-1-4939-6671-4, 978-1-4939-6673-8
|
Authors |
Cindy Fevre, Lisette Scheepmaker, Pieter-Jan Haas |
Editors |
Pontus Nordenfelt, Mattias Collin |
Abstract |
Methods aimed at identification of immune evasion proteins are mainly rely on in silico prediction of sequence, structural homology to known evasion proteins or use a proteomics driven approach. Although proven successful these methods are limited by a low efficiency and or lack of functional identification. Here we describe a high-throughput genomic strategy to functionally identify bacterial immune evasion proteins using phage display technology. Genomic bacterial DNA is randomly fragmented and ligated into a phage display vector that is used to create a phage display library expressing bacterial secreted and membrane bound proteins. This library is used to select displayed bacterial secretome proteins that interact with host immune components. |
Mendeley readers
Geographical breakdown
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Unknown | 10 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 2 | 20% |
Researcher | 2 | 20% |
Student > Master | 2 | 20% |
Student > Bachelor | 1 | 10% |
Librarian | 1 | 10% |
Other | 0 | 0% |
Unknown | 2 | 20% |
Readers by discipline | Count | As % |
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Veterinary Science and Veterinary Medicine | 1 | 10% |
Arts and Humanities | 1 | 10% |
Computer Science | 1 | 10% |
Immunology and Microbiology | 1 | 10% |
Other | 1 | 10% |
Unknown | 3 | 30% |