Division of Bioengineering, School of Chemical & Biomedical Engineering, Nanyang Technological University, Singapore 637457.
ACS Nano. 2013 Jul 23;7(7):6278-86. doi: 10.1021/nn4023137. Epub 2013 Jun 27.
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.
石墨烯量子点 (GQDs) 由于其可调谐的光致发光、优异的光稳定性和生物相容性等显著的物理化学性质,有望成为一类新的用于生物成像的荧光团。尽管它们具有很高的预期潜力,但 GQDs 尚未被用于特异性标记和跟踪活细胞中动态细胞过程中涉及的分子靶标。在这里,我们证明 GQDs 可以作为生物成像的通用荧光团,因为它们可以很容易地与各种生物分子偶联,同时保持其功能。作为概念验证演示,我们合成了胰岛素偶联的 GQDs,并将其用于特异性标记和动态跟踪 3T3-L1 脂肪细胞中的胰岛素受体。我们的实验首次揭示,脂肪细胞中胰岛素受体的内化和再循环受 Apelin 和 TNFα 的相反调节,这可能有助于调节这两种细胞因子对胰岛素敏感性的影响。