Properties of GluR3 receptors tagged with GFP at the amino or carboxyl terminus

Agenor Limon-Ruiz, Jorge Mauricio Reyes-Ruiz, Fabrizio Eusebi, Ricardo Miledi

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Anatomical visualization of neurotransmitter receptor localization is facilitated by tagging receptors, but this process can alter their functional properties. We have evaluated the distribution and properties of WT glutamate receptor 3 (GluR3) α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors (WT GluR3) and two receptors in which GFP was tagged to the amino terminus (GFP-GluR3) or to the carboxyl terminus (GluR3-GFP). Although the fluorescence in Xenopus oocytes was stronger in the vegetal hemisphere because of localization of internal structures (probable sites of production, storage or recycling of receptors), the insertion of receptors into the plasma membrane was polarized to the animal hemisphere. The fluorescence intensity of oocytes injected with GluR3-GFP RNA was approximately double that of oocytes injected with GFP-GluR3 RNA. Accordingly, GluR3-GFP oocytes generated larger kainate-induced currents than GFP-GluR3 oocytes, with similar EC50 values. Currents elicited by glutamate, or AMPA coapplied with cyclothiazide, were also larger in GluR3-GFP oocytes. The glutamate- to kainate-current amplitude ratios differed, with GluR3-GFP being activated more efficiently by glutamate than the WT or GFP-GluR3 receptors. This pattern correlates with the slower decay of glutamate-induced currents generated by GluR3-GFP receptors. These changes were not observed when GFP was tagged to the amino terminus, and these receptors behaved like the WT. The antagonistic effects of 6-nitro-7-sulfamoylbenzo-[f]quinoxaline-2,3-dione (NBQX) and 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) were not altered in any of the tagged receptors. We conclude that GFP is a useful and convenient tag for visualizing these proteins. However, the effects of different sites of tag insertion on receptor characteristics must be taken into account in assessing the roles played by these receptor proteins. fluorescent tag receptor expression Xenopus oocytes kainate glutamate

Original languageEnglish (US)
Pages (from-to)15526-15530
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume104
Issue number39
DOIs
StatePublished - Sep 25 2007
Externally publishedYes

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Glutamate Receptors
Oocytes
Glutamic Acid
Kainic Acid
Xenopus
Fluorescence
RNA
6-Cyano-7-nitroquinoxaline-2,3-dione
Isoxazoles
alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
Neurotransmitter Receptor
AMPA Receptors
Proteins
Cell Membrane

ASJC Scopus subject areas

  • Genetics
  • General

Cite this

Properties of GluR3 receptors tagged with GFP at the amino or carboxyl terminus. / Limon-Ruiz, Agenor; Reyes-Ruiz, Jorge Mauricio; Eusebi, Fabrizio; Miledi, Ricardo.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, No. 39, 25.09.2007, p. 15526-15530.

Research output: Contribution to journalArticle

Limon-Ruiz, Agenor ; Reyes-Ruiz, Jorge Mauricio ; Eusebi, Fabrizio ; Miledi, Ricardo. / Properties of GluR3 receptors tagged with GFP at the amino or carboxyl terminus. In: Proceedings of the National Academy of Sciences of the United States of America. 2007 ; Vol. 104, No. 39. pp. 15526-15530.
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