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.
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October 2013
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Conference Article|
September 23 2013
Rational design of FRET sensor proteins based on mutually exclusive domain interactions
Maarten Merkx;
Maarten Merkx
1
*Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, 5600MB Eindhoven, The Netherlands
1email [email protected]
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Misha V. Golynskiy;
Misha V. Golynskiy
*Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, 5600MB Eindhoven, The Netherlands
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Laurens H. Lindenburg;
Laurens H. Lindenburg
*Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, 5600MB Eindhoven, The Netherlands
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Jan L. Vinkenborg
Jan L. Vinkenborg
*Laboratory of Chemical Biology, Department of Biomedical Engineering, Eindhoven University of Technology, P.O. Box 513, 5600MB Eindhoven, The Netherlands
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Publisher: Portland Press Ltd
Received:
July 02 2013
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© 2013 The Authors
2013
Biochem Soc Trans (2013) 41 (5): 1201–1205.
Article history
Received:
July 02 2013
Citation
Maarten Merkx, Misha V. Golynskiy, Laurens H. Lindenburg, Jan L. Vinkenborg; Rational design of FRET sensor proteins based on mutually exclusive domain interactions. Biochem Soc Trans 1 October 2013; 41 (5): 1201–1205. doi: https://doi.org/10.1042/BST20130128
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