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NLRP3 Phospho-residue Mapping by Phospho Dot Blots

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The Inflammasome

Part of the book series: Methods in Molecular Biology ((MIMB,volume 2459))

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Abstract

When characterizing posttranslational modifications like phosphorylation, using efficient screening methods to map the phospho sites is essential, especially when dealing with large multi-domain proteins. NLRP3 (the NOD, LRR, and pyrin domain-containing protein 3), which initiates the formation of an NLRP3 inflammasome complex, is regulated posttranslationally by phosphorylation at several Ser and Tyr residues. However, determining sites of modification are not straightforward. For quick and reliable screening of the candidate phospho sites in NLRP3, we use a phospho dot blot assay which we describe here. This technique employs an in vitro kinase assay with a candidate kinase, Bruton’s Tyrosine Kinase (BTK), and peptides derived from the region of interest in the protein that contains the potential phosphorylation sites. The reaction containing the phosphorylated peptides is quickly screened by a dot blot where the peptides are blotted with a commercially available anti-phospho-tyrosine antibody. This method can also be adapted to detect modified Ser or Thr residues and is an ideal screening assay to map phospho residues in NLRP3 or other proteins. This can be an initial screening procedure or can be complemented by other approaches such as site directed mutagenesis and by generating phospho site-specific antibodies.

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Acknowledgments

We thank Xiaowu Zhang from Cell Signaling Technologies for helpful advice on the initial conceptual implementation of this method. The work was supported by the Else-Kröner-Fresenius Stiftung (to A.W.), the Deutsche Forschungsgemeinschaft (German Research Foundation, DFG) grant We-4195/15-1 (to A.W.), and the University Hospital Tübingen. Infrastructural funding was provided by the University of Tübingen, the University Hospital Tübingen, and the DFG Clusters of Excellence “iFIT—Image-Guided and Functionally Instructed Tumor Therapies” (EXC 2180, to AW), “CMFI—Controlling Microbes to Fight Infection” (EXC 2124, to AW), Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) im Rahmen der Exzellenzstrategie des Bundes und der Länder—EXC 2180 and EXC 2124.

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Correspondence to Alexander N. R. Weber .

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Shankar, S., Bittner, Z.A., Weber, A.N.R. (2022). NLRP3 Phospho-residue Mapping by Phospho Dot Blots. In: Abdul-Sater, A.A. (eds) The Inflammasome. Methods in Molecular Biology, vol 2459. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2144-8_10

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  • DOI: https://doi.org/10.1007/978-1-0716-2144-8_10

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-2143-1

  • Online ISBN: 978-1-0716-2144-8

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