A Gateway-based system for fast evaluation of protein-protein interactions in bacteria

• Verfasst von: Wille, Thorsten [VerfasserIn]
• Verfasst von: Barlag, Britta [VerfasserIn]
• Verfasst von: Jakovljević, Vladimir [VerfasserIn]
• Verfasst von: Hensel, Michael [VerfasserIn]
• Verfasst von: Sourjik, Victor [VerfasserIn]
• Verfasst von: Gerlach, Roman G. [VerfasserIn]
• Titel: A Gateway-based system for fast evaluation of protein-protein interactions in bacteria
• Verf.angabe: Thorsten Wille, Britta Barlag, Vladimir Jakovljevic, Michael Hensel, Victor Sourjik, Roman G. Gerlach
• E-Jahr: 2015
• Jahr: April 9, 2015
• Fussnoten: Gesehen am 02.07.2020
• Titel Quelle: Enthalten in: PLOS ONE
• Ort Quelle: San Francisco, California, US : PLOS, 2006
• Jahr Quelle: 2015
• Band/Heft Quelle: 10(2015,4) Artikel-Nummer e0123646, 18 Seiten
• ISSN Quelle: 1932-6203
• DOI: doi:10.1371/journal.pone.0123646
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Cloning
• Sach-SW: Fluorescence resonance energy transfer
• Sach-SW: Gene fusion
• Sach-SW: Protein-protein interactions
• Sach-SW: Recombination reactions
• Sach-SW: Reporter genes
• Sach-SW: Salmonella typhimurium
• Sach-SW: Vector cloning
• K10plus-PPN: 1703271173

Abstract

Protein-protein interactions are important layers of regulation in all kingdoms of life. Identification and characterization of these interactions is one challenging task of the post-genomic era and crucial for understanding of molecular processes within a cell. Several methods have been successfully employed during the past decades to identify protein-protein interactions in bacteria, but most of them include tedious and time-consuming manipulations of DNA. In contrast, the MultiSite Gateway system is a fast tool for transfer of multiple DNA fragments between plasmids enabling simultaneous and site directed cloning of up to four fragments into one construct. Here we developed a new set of Gateway vectors including custom made entry vectors and modular Destination vectors for studying protein-protein interactions via Fluorescence Resonance Energy Transfer (FRET), Bacterial two Hybrid (B2H) and split Gaussia luciferase (Gluc), as well as for fusions with SNAP-tag and HaloTag for dual-color super-resolution microscopy. As proof of principle, we characterized the interaction between the Salmonella effector SipA and its chaperone InvB via split Gluc and B2H approach. The suitability for FRET analysis as well as functionality of fusions with SNAP- and HaloTag could be demonstrated by studying the transient interaction between chemotaxis response regulator CheY and its phosphatase CheZ.