Literature DB >> 35759197

A Surface Plasmon Resonance-Based Strategy to Characterize Interactions of NLR Proteins with Associated Factors.

Jonas Moecking1, Matthias Geyer2.   

Abstract

NOD-like receptors (NLRs) are established as key regulators of the innate immune system. In recent years, an increasing number of interaction partners have been described that modulate receptor activity by direct binding. Characterizing these interactions can be challenging because these receptors tend to adopt different conformational states. We have developed a protocol that employs intracellular protein biotinylation to provide a straightforward immobilization strategy in surface plasmon resonance experiments. With this highly sensitive and label-free technique, the kinetics and affinities of NLR and co-factor interactions can be measured directly at the protein level.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Affinity; Biotinylation; Kinetics; NOD-like receptor (NLR); Protein–protein interaction; Surface plasmon resonance (SPR)

Mesh:

Substances:

Year:  2022        PMID: 35759197     DOI: 10.1007/978-1-0716-2449-4_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Structures and mechanism of dipeptidyl peptidases 8 and 9, important players in cellular homeostasis and cancer.

Authors:  Breyan Ross; Stephan Krapp; Martin Augustin; Reiner Kierfersauer; Marcelino Arciniega; Ruth Geiss-Friedlander; Robert Huber
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-30       Impact factor: 11.205

  1 in total

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