Chemistry Department, Princeton University, Princeton, New Jersey 08544, USA.
Nat Nanotechnol. 2014 Mar;9(3):198-203. doi: 10.1038/nnano.2014.12. Epub 2014 Feb 23.
A detailed understanding of the cellular uptake process is essential to the development of cellular delivery strategies and to the study of viral trafficking. However, visualization of the entire process, encompassing the fast dynamics (local to the freely diffusing nanoparticle) as well the state of the larger-scale cellular environment, remains challenging. Here, we introduce a three-dimensional multi-resolution method to capture, in real time, the transient events leading to cellular binding and uptake of peptide (HIV1-Tat)-modified nanoparticles. Applying this new method to observe the landing of nanoparticles on the cellular contour in three dimensions revealed long-range deceleration of the delivery particle, possibly due to interactions with cellular receptors. Furthermore, by using the nanoparticle as a nanoscale 'dynamics pen', we discovered an unexpected correlation between small membrane terrain structures and local nanoparticle dynamics. This approach could help to reveal the hidden mechanistic steps in a variety of multiscale processes.
深入了解细胞摄取过程对于开发细胞递药策略和研究病毒运输至关重要。然而,要可视化整个过程(包括快速动力学(自由扩散纳米颗粒的局部)以及更大规模细胞环境的状态)仍然具有挑战性。在这里,我们引入了一种三维多分辨率方法,实时捕获导致肽(HIV1-Tat)修饰的纳米颗粒与细胞结合和摄取的瞬态事件。应用这种新方法观察纳米颗粒在三维空间上在细胞轮廓上的着陆,揭示了递药颗粒的远程减速,这可能是由于与细胞受体的相互作用。此外,通过将纳米颗粒用作纳米级“动态笔”,我们发现了小膜地形结构与局部纳米颗粒动力学之间出乎意料的相关性。这种方法可以帮助揭示各种多尺度过程中的隐藏机制步骤。