Literature DB >> 28439869

Studying Protein-Protein Interactions In Planta Using Advanced Fluorescence Microscopy.

Marc Somssich1,2, Rüdiger Simon3.   

Abstract

The formation of protein complexes through direct protein-protein interaction is essential for virtually every biological process, and accordingly the ability to determine the interaction properties of specific proteins is important to understand these processes. Förster resonance energy transfer (FRET) measurements are state-of-the-art confocal fluorescence microscopy- and imaging-based techniques that allow the analysis of protein interactions in vivo and in planta, in specific compartments of single cells or tissues. Here we provide a step-by-step guide to perform FRET measurements by acceptor photobleaching (APB) and fluorescence lifetime imaging microscopy (FLIM) in the plant expression system Nicotiana benthamiana.

Entities:  

Keywords:  APB; Acceptor photobleaching; Confocal fluorescence microscopy; FLIM; FRET; Fluorescence lifetime; Live cell imaging; Nicotiana benthamiana; Protein–protein interaction

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Year:  2017        PMID: 28439869     DOI: 10.1007/978-1-4939-7003-2_17

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Studying Protein-Protein Interactions at Plasmodesmata by Measuring Förster Resonance Energy Transfer.

Authors:  Patrick Blümke; Vicky Howe; Rüdiger Simon
Journal:  Methods Mol Biol       Date:  2022

2.  Over the rainbow: A practical guide for fluorescent protein selection in plant FRET experiments.

Authors:  Grégoire Denay; Patrick Schultz; Sebastian Hänsch; Stefanie Weidtkamp-Peters; Rüdiger Simon
Journal:  Plant Direct       Date:  2019-12-06
  2 in total

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