内吞循环
DNA
量子点
表面改性
纳米技术
DNA折纸
化学
材料科学
配体(生物化学)
生物物理学
受体
生物化学
内吞作用
生物
物理化学
作者
Dhiraj Bhatia,Senthil Arumugam,Michel Nasilowski,Himanshu Joshi,Christian Wunder,Valérie Chambon,Ved Prakash,Chloé Grazon,Brice Nadal,Prabal K. Maiti,Ludger Johannes,Benoît Dubertret,Yamuna Krishnan
标识
DOI:10.1038/nnano.2016.150
摘要
Functionalization of quantum dots (QDs) with a single biomolecular tag using traditional approaches in bulk solution has met with limited success. DNA polyhedra consist of an internal void bounded by a well-defined three-dimensional structured surface. The void can house cargo and the surface can be functionalized with stoichiometric and spatial precision. Here, we show that monofunctionalized QDs can be realized by encapsulating QDs inside DNA icosahedra and functionalizing the DNA shell with an endocytic ligand. We deployed the DNA-encapsulated QDs for real-time imaging of three different endocytic ligands-folic acid, galectin-3 (Gal3) and the Shiga toxin B-subunit (STxB). Single-particle tracking of Gal3- or STxB-functionalized QD-loaded DNA icosahedra allows us to monitor compartmental dynamics along endocytic pathways. These DNA-encapsulated QDs, which bear a unique stoichiometry of endocytic ligands, represent a new class of molecular probes for quantitative imaging of endocytic receptor dynamics.
科研通智能强力驱动
Strongly Powered by AbleSci AI