Bottini Massimo, Cerignoli Fabio, Dawson Marcia I, Magrini Andrea, Rosato Nicola, Mustelin Tomas
Burnham Institute for Medical Research, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.
Biomacromolecules. 2006 Aug;7(8):2259-63. doi: 10.1021/bm0602031.
We report the formation of a supramolecular luminescent nanoassembly composed of individual or small ropes of full-length, single-walled carbon nanotubes decorated with streptavidin-conjugated quantum dots. The supramolecular luminescent nanoassembly was stably dispersed under physiological conditions and was readily visible by both optical and confocal fluorescent microscopies. Jurkat T leukemia cells were able to internalize the nanoassembly by multivalent CD3 receptor-mediated endocytosis (adsorption by cell). Once internalized by cells, the nanoassembly was found to be transported to lysosomes. These properties should make this supramolecular luminescent nanoassembly an excellent building block for the construction of intracellular polyvalent nanoprobes, mimicking natural viral delivery entities with enhanced loading capacity compared to small molecules.
我们报道了一种超分子发光纳米组装体的形成,该组装体由全长单壁碳纳米管的单个或小束组成,这些碳纳米管上装饰有链霉亲和素偶联的量子点。这种超分子发光纳米组装体在生理条件下稳定分散,通过光学显微镜和共聚焦荧光显微镜都很容易观察到。Jurkat T白血病细胞能够通过多价CD3受体介导的内吞作用(细胞吸附)内化该纳米组装体。一旦被细胞内化,该纳米组装体被发现会被转运到溶酶体。这些特性应使这种超分子发光纳米组装体成为构建细胞内多价纳米探针的优秀构建块,可模拟天然病毒递送实体,与小分子相比具有更高的负载能力。