Plate-based assay for measuring direct semaphorin-neuropilin interactions

Matthew W. Parker, Craig W. Vander Kooi

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The semaphorins are an essential family of axon guidance molecules that can be either secreted or are transmembrane proteins. Class 3 semaphorin (Sema3) family members are secreted and provide longrange guidance cues through two receptor families: neuropilins (Nrp) and plexins. Nrp is uniquely required for high-affinity Sema3 binding and signaling. Therefore, characterizing the molecular details of the Sema3/Nrp interaction is important for understanding the broader physiological and pathological role of the Sema3 family of proteins. Here we describe an in vitro plate-based binding assay for characterization of the Sema3/Nrp interaction. This assay utilizes Nrp-affinity plates and an alkaline phosphatase (AP)-Sema3 fusion to rapidly measure direct Sema3/Nrp binding. This assay can be used to measure receptorligand binding, the contribution of different domains, and exogenous factors, and to characterize competitive ligand binding.

Original languageEnglish
Pages (from-to)73-87
Number of pages15
JournalMethods in Molecular Biology
Volume1493
DOIs
StatePublished - 2017

Bibliographical note

Publisher Copyright:
© Springer Science+Business Media New York 2017.

Funding

This work was supported by National Institutes of Health grants R01GM094155 (C.W.V.K.) and T32HL072743 (M.W.P.)

FundersFunder number
National Institutes of Health (NIH)T32HL072743
National Institute of General Medical SciencesR01GM094155

    Keywords

    • Assay
    • Binding
    • Competition
    • Interaction
    • Ligand
    • Neuropilin
    • Plate-based
    • Receptor
    • Semaphorin

    ASJC Scopus subject areas

    • Molecular Biology
    • Genetics

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