| Literature DB >> 24059509 |
Maarten Merkx1, Misha V Golynskiy, Laurens H Lindenburg, Jan L Vinkenborg.
Abstract
Proteins that switch between distinct conformational states are ideal to monitor and control molecular processes within the complexity of biological systems. Inspired by the modular architecture of natural signalling proteins, our group explores generic design strategies for the construction of FRET-based sensor proteins and other protein switches. In the present article, I show that designing FRET sensors based on mutually exclusive domain interactions provides a robust method to engineer sensors with predictable properties and an inherently large change in emission ratio. The modularity of this approach should make it easily transferable to other applications of protein switches in fields ranging from synthetic biology, optogenetics and molecular diagnostics.Entities:
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Year: 2013 PMID: 24059509 PMCID: PMC3822149 DOI: 10.1042/BST20130128
Source DB: PubMed Journal: Biochem Soc Trans ISSN: 0300-5127 Impact factor: 5.407