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Title: Graphene quantum dots as universal fluorophores and their use in revealing regulated trafficking of insulin receptors in adipocytes
Authors: Zheng, Xin Ting
Than, Aung
Ananthanaraya, Arundithi
Kim, Dong-Hwan
Chen, Peng
Keywords: DRNTU::Engineering::Chemical engineering::Biochemical engineering
Issue Date: 2013
Source: Zheng, X. T., Than, A., Ananthanaraya, A., Kim, D. H., & Chen, P. (2013). Graphene Quantum Dots as Universal Fluorophores and Their Use in Revealing Regulated Trafficking of Insulin Receptors in Adipocytes. ACS Nano, 7(7), 6278-6286.
Series/Report no.: ACS nano
Abstract: Graphene quantum dots (GQDs) hold great promise as a new class of fluorophores for bioimaging, owing to their remarkable physicochemical properties including tunable photoluminescence, excellent photostability, and biocompatibility. Despite their highly anticipated potentials, GQDs have yet to be used to specifically label and track molecular targets involved in dynamic cellular processes in live cells. Here, we demonstrate that GQDs can serve as universal fluorophores for bioimaging because they can be readily conjugated with a wide range of biomolecules while preserving their functionalities. As a proof-of-concept demonstration, insulin-conjugated GQDs have been synthesized and utilized for specific labeling and dynamic tracking of insulin receptors in 3T3-L1 adipocytes. Our experiments reveal, for the first time, that the internalization and recycling of insulin receptors in adipocytes are oppositely regulated by apelin and TNFα, which may contribute to the regulations of these two cytokines in insulin sensitivity.
ISSN: 1936-086X
DOI: 10.1021/nn4023137
Rights: © 2013 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by ACS nano, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [].
Fulltext Permission: open
Fulltext Availability: With Fulltext
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