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Cell-based enzyme-linked immunosorbent assay (cell-ELISA) analysis of native and recombinant glutamate receptors

Research output: Chapter in Book/Report/Conference proceedingChapter in a book

Original languageEnglish
Title of host publicationMethods in Molecular Biology
Subtitle of host publicationGlutamate receptors: Methods and protocols
Publisher or commissioning bodySpringer
Number of pages8
ISBN (Print)978-1-4939-9077-1
DateE-pub ahead of print - 2 Feb 2019
DatePublished (current) - 23 Mar 2019

Publication series

NameMethods in Molecular Biology
ISSN (Print)1064-3745


Glutamate receptors (GluRs) located primarily on the membranes of neurons and glial cells are responsible for excitatory synaptic transmission in the central nervous system. The transport of GluRs to the cell surface is a highly regulated dynamic process that determines neuronal excitability and synaptic responses. The molecular and cellular mechanisms of GluR trafficking are often studied in cell cultures. These studies require sensitive techniques that allow the measurement of total and surface expressed GluRs in cell populations. The cell-based enzyme-linked immunosorbent assay (cell-ELISA) combines steps of direct immunochemical labelling of cell cultures and ELISA. It can be used for quantitative comparisons of surface expressed and total protein contents of various cell cultures. While several cell-ELISA protocols are available for different cell types, in this chapter we describe the procedure that we have applied for the investigation of quantitative changes in the cell surface expression of recombinant ionotropic glutamate receptors (iGluRs) in adherent human embryonic kidney 293 (HEK293) cells and endogenous iGluR proteins in primary neuronal cultures.

    Research areas

  • Antibodies, Cell-ELISA, Cell surface protein, Glutamate receptor, Neuronal culture, Targeting, trafficking, Neurochemistry, Receptors, Membrane proteins, Cell biology, Cell culture



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