Department of Chemistry, University of Massachusetts-Amherst, 710 North Pleasant Street, Amherst, Massachusetts, 01003, USA.
ACS Nano. 2013 Aug 27;7(8):6667-6673. doi: 10.1021/nn402753y. Epub 2013 Jul 8.
Intracellular protein delivery is an important tool for both therapeutic and fundamental applications. Effective protein delivery faces two major challenges: efficient cellular uptake and avoiding endosomal sequestration. We report here a general strategy for direct delivery of functional proteins to the cytosol using nanoparticle-stabilized capsules (NPSCs). These NPSCs are formed and stabilized through supramolecular interactions between the nanoparticle, the protein cargo, and the fatty acid capsule interior. The NPSCs are ~130 nm in diameter and feature low toxicity and excellent stability in serum. The effectiveness of these NPSCs as therapeutic protein carriers was demonstrated through the delivery of fully functional caspase-3 to HeLa cells with concomitant apoptosis. Analogous delivery of green fluorescent protein (GFP) confirmed cytosolic delivery as well as intracellular targeting of the delivered protein, demonstrating the utility of the system for both therapeutic and imaging applications.
细胞内蛋白质递送是治疗和基础应用的重要工具。有效的蛋白质递送面临两个主要挑战:高效的细胞摄取和避免内涵体隔离。我们在这里报告了一种使用纳米颗粒稳定的胶囊(NPSC)将功能性蛋白质直接递送到细胞质中的通用策略。这些 NPSC 通过纳米颗粒、蛋白质货物和脂肪酸胶囊内部之间的超分子相互作用形成和稳定。NPSC 的直径约为 130nm,具有低毒性和优异的血清稳定性。通过将完全功能性的 caspase-3 递送到 HeLa 细胞中并伴随细胞凋亡,证明了这些 NPSC 作为治疗性蛋白质载体的有效性。类似地递送达 GFP 证实了细胞质内递送到递送到的蛋白质的细胞内靶向,展示了该系统在治疗和成像应用中的实用性。