Fluorescent Exendin-4 Derivatives for Pancreatic [Beta]-Cell Analysis

The ability to reliably identify pancreatic β-cells would have far reaching implications for a greater understanding of β-cell biology, measurement of β-cell mass in diabetes, islet transplantation, and drug development. The glucagon-like peptide-1 receptor (GLP1R) is highly expressed on the surface...

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Veröffentlicht in:Bioconjugate chemistry 2014-01, Vol.25 (1), p.171
Hauptverfasser: Clardy, Susan M, Keliher, Edmund J, Mohan, James F, Sebas, Matt, Benoist, Christophe, Mathis, Diane, Weissleder, Ralph
Format: Artikel
Sprache:eng
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Zusammenfassung:The ability to reliably identify pancreatic β-cells would have far reaching implications for a greater understanding of β-cell biology, measurement of β-cell mass in diabetes, islet transplantation, and drug development. The glucagon-like peptide-1 receptor (GLP1R) is highly expressed on the surface of insulin producing pancreatic β-cells. Using systematic modifications of the GLP1R ligand, exendin-4, we screened over 25 compounds and identified a palette of fluorescent exendin-4 with high GLP1R binding affinity. We show considerable differences in affinity, as well as utility of the top candidates for flow cytometry and microscopy of β-cells. Some of the developed compounds should be particularly useful for basic and translational β-cell research. [PUBLICATION ABSTRACT]
ISSN:1043-1802
1520-4812