A field-proven yeast two-hybrid protocol used to identify coronavirus-host protein-protein interactions
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Publication date
2015-02-26
Editors
Maier, Helena Jane
Bickerton, Erica
Britton, Paul
Advisors
Supervisors
Document Type
Part of book
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taverne
Abstract
Over the last 2 decades, yeast two-hybrid became an invaluable technique to decipher protein-protein interaction networks. In the field of virology, it has proven instrumental to identify virus-host interactions that are involved in viral embezzlement of cellular functions and inhibition of immune mechanisms. Here, we present a yeast two-hybrid protocol that has been used in our laboratory since 2006 to search for cellular partners of more than 300 viral proteins. Our aim was to develop a robust and straightforward pipeline, which minimizes false-positive interactions with a decent coverage of target cDNA libraries, and only requires a minimum of equipment. We also discuss reasons that motivated our technical choices and compromises that had to be made. This protocol has been used to screen most non-structural proteins of murine hepatitis virus (MHV), a member of betacoronavirus genus, against a mouse brain cDNA library. Typical results were obtained and are presented in this report.
Keywords
Host-pathogen interactions, Interactomics, Murine hepatitis virus, Proteomics, Yeast two-hybrid, Taverne, General Immunology and Microbiology, General Medicine, Journal Article, Research Support, Non-U.S. Gov't
Citation
Vidalain, P O, Jacob, Y, Hagemeijer, M C, Jones, L M, Neveu, G, Roussarie, J P, Rottier, P J M, Tangy, F & De Haan, C A M 2015, A field-proven yeast two-hybrid protocol used to identify coronavirus-host protein-protein interactions. in H J Maier, E Bickerton & P Britton (eds), Coronaviruses: Methods and Protocols. vol. V, Methods in Molecular Biology, vol. 1282, Springer New York, pp. 213-229. https://doi.org/10.1007/978-1-4939-2438-7_18