Understanding the synergistic effect of physicochemical properties of nanoparticles and their cellular entry pathways.

Gaining precise control over the cellular entry pathway of nanomaterials is key in achieving cytosolic delivery, accessing subcellular environments, and regulating toxicity. However, this precise control requires a fundamental understanding of the behavior of nanomaterials at the bio-nano interface. Herein, we report a computational study investigating the synergistic effect of several key physicochemical properties of nanomaterials on their cellular entry pathways. By examining interactions between monolayer-protected nanoparticles and model cell membranes in a three-dimensional parameter space of size, surface charge/pKa, and ligand chemistry, we observed four different types of nanoparticle translocation for cellular entry which are: outer wrapping, free translocation, inner attach, and embedment. Nanoparticle size, surface charge/pKa, and ligand chemistry each play a unique role in determining the outcome of translocation. Specifically, membrane local curvature induced by nanoparticles upon contact is critical for initiating the translocation process. A generalized paradigm is proposed to describe the fundamental mechanisms underlying the bio-nano interface. Lin et al. investigate interactions between monolayer-protected nanoparticles and model cell membranes, and show four different types of nanoparticle translocation, i.e., outer wrapping, free translocation, inner attach, and embedment. The different translocation types greatly depend on synergism between nanoparticle size, surface charge, and ligand chemistry. [ABSTRACT FROM AUTHOR]