Journal article

Salmonella effectors SseK1 and SseK3 target death domain proteins in the TNF and TRAIL signaling pathways

JPM Newson, NE Scott, IYW Chung, TWF Lung, C Giogha, J Gan, N Wang, RA Strugnell, NF Brown, M Cygler, JS Pearson, EL Hartland

Molecular and Cellular Proteomics | Published : 2019

Abstract

Strains of Salmonella utilize two distinct type three secretion systems to deliver effector proteins directly into host cells. The Salmonella effectors SseK1 and SseK3 are arginine glycosyltransferases that modify mammalian death domain containing proteins with N-acetyl glucosamine (GlcNAc) when overexpressed ectopically or as recombinant protein fusions. Here, we combined Arg-GlcNAc gly-copeptide immunoprecipitation and mass spectrometry to identify host proteins GlcNAcylated by endogenous levels of SseK1 and SseK3 during Salmonella infection. We observed that SseK1 modified the mammalian signaling protein TRADD, but not FADD as previously reported. Overexpression of SseK1 greatly broadened..

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Funding Acknowledgements

Graphical abstract was created with Bio-Render. We are indebted to Jurg Tschopp for the gift of pFlag-TRADD. Research described in this paper was performed using beamline 08B1-1 and 08ID-1 at the Canadian Light Source, which is supported by the Canada Foundation for Innovation, Natural Sciences and Engineering Research Council of Canada, the University of Saskatchewan, the Government of Saskatchewan, Western Economic Diversification Canada, the National Research Council Canada, and the Canadian Institutes of Health Research.