Signalling by pattern recognition receptors (PRRs) is critical for protecting the host against pathogens. Disruption of these signalling pathways has been implicated in many diseases ranging from infection susceptibility to cancer and autoimmune disease. Understanding how PRRs signal is of critical importance due to their potential as therapeutic targets to ameliorate symptoms of inflammatory diseases. The recent advances in microscopy, such as the discovery of fluorescent proteins and the breaking of the diffraction limit of light, offer a unique opportunity to visualise receptor signalling at a single protein level within living cells. Many different microscopy techniques have been developed and used for dissecting different aspects of PRR signalling pathways. This review will provide an overview of the main microscopy techniques used for dissecting these pathways with a focus on Toll-like receptor and NOD-like receptor signalling.
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Cover Image
Cover Image
The Holliday junction. The structure of the Holliday junction is highly variable, being adaptable to its biological function in recombination and to applications in biomolecular engineering. This image shows the how the junction extends from simple schematics to crystal structures as DNA only and in protein complexes. In addition, the junction has been exploited as an element in the design of 2-D and 3-D lattices in crystal engineering and more complex images and shapes through DNA origami. In this issue of Biochemical Society Transactions, P. Shing Ho reviews some interesting recent research on the Holliday junction; for details see pages 1149–1158.
Visualising pattern recognition receptor signalling
Charlotte Macleod, Clare E. Bryant; Visualising pattern recognition receptor signalling. Biochem Soc Trans 15 October 2017; 45 (5): 1077–1085. doi: https://doi.org/10.1042/BST20160459
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