Ligand-binding assays with OBPs and CSPs

Chiara D´Onofrio, Valeriia Zaremska, Jiao Zhu, Wolfgang Knoll, Paolo Pelosi

    Research output: Chapter in Book or Conference ProceedingsBook chapter

    Abstract

    Assessing the ligand-binding properties of OBPs and CSPs is essential for understanding their physiological function. It also provides basic information when these proteins are used as biosensing elements for instrumental measurement of odors. Although different approaches have been applied in the past to evaluate the affinity of receptors and soluble binding proteins to their ligands, using a fluorescent reporter represents the method of choice for OBPs and CSPs. It offers the advantages of working at the equilibrium, being simple, fast and inexpensive, without requiring the use of radioactive tracers. However, as an indirect method, the fluorescence competitive binding approach presents drawbacks and sometimes requires an elaborate analysis to explain unexpected results. Here, after a brief survey of the different approaches to evaluate affinity constants, we focus on the fluorescence binding assay as applied to OBPs and CSPs, discussing situations that may require closer inspection of the results.
    Original languageEnglish
    Title of host publicationMethods in Enzymology
    EditorsPaolo Pelosi, Wolfgang Knoll
    PublisherElsevier
    Pages229-258
    Number of pages30
    Volume642
    DOIs
    Publication statusPublished - 2020

    Research Field

    • Biosensor Technologies

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