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Detecting ligand in...
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Xu, BoUppsala universitet,Farmakologi
(författare)
Detecting ligand interactions with G protein-coupled receptors in real-time on living cells
- Artikel/kapitelEngelska2013
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Elsevier BV,2013
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LIBRIS-ID:oai:DiVA.org:uu-215943
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-215943URI
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https://doi.org/10.1016/j.bbrc.2013.10.149DOI
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Språk:engelska
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Sammanfattning på:engelska
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G protein-coupled receptors (GPCRs) are a large group of receptors of great biological and clinical relevance. Despite this, the tools for a detailed analysis of ligand-GPCR interactions are limited. The aim of this paper was to demonstrate how ligand binding to GPCRs can be followed in real-time on living cells. This was conducted using two model systems, the radiolabeled porcine peptide YY (pPYY) interacting with transfected human Y2 receptor (hY2R) and the bombesin antagonist RM26 binding to the naturally expressed gastrin-releasing peptide receptor (GRPR). By following the interaction over time, the affinity and kinetic properties such as association and dissociation rate were obtained. Additionally, data were analyzed using the Interaction Map method, which can evaluate a real-time binding curve and present the number of parallel interactions contributing to the curve. It was found that pPYY binds very slowly with an estimated time to equilibrium of approximately 12 h. This may be problematic in standard end-point assays where equilibrium is required. The RM26 binding showed signs of heterogeneity, observed as two parallel interactions with unique kinetic properties. In conclusion, measuring binding in real-time using living cells opens up for a better understanding of ligand interactions with GPCRs.
Ämnesord och genrebeteckningar
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GPCR
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Real-time
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LigandTracer
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Interaction Map
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Kinetics
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Heterogeneity
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Uppsala universitetFarmakologi
(creator_code:org_t)
Sammanhörande titlar
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Ingår i:Biochemical and Biophysical Research Communications - BBRC: Elsevier BV441:4, s. 820-8240006-291X1090-2104
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