Department of Chemistry, University of Massachusetts , 710 North Pleasant Street, Amherst, Massachusetts 01003, United States.
ACS Nano. 2017 Jun 27;11(6):6416-6421. doi: 10.1021/acsnano.7b02884. Epub 2017 Jun 15.
Endosomal entrapment is a key hurdle for most intracellular protein-based therapeutic strategies. We report a general strategy for efficient delivery of proteins to the cytosol through co-engineering of proteins and nanoparticle vehicles. The proteins feature an oligo(glutamate) sequence (E-tag) that binds arginine-functionalized gold nanoparticles, generating hierarchical spherical nanoassemblies. These assemblies fuse with cell membranes, releasing the E-tagged protein directly into the cytosol. Five different proteins with diverse charges, sizes, and functions were effectively delivered into cells, demonstrating the generality of our method. Significantly, the engineered proteins retained activity after cytosolic delivery, as demonstrated through the delivery of active Cre recombinase, and granzyme A to kill cancer cells.
内体捕获是大多数基于细胞内蛋白质的治疗策略的一个关键障碍。我们报告了一种通过蛋白质和纳米颗粒载体的协同工程化将蛋白质有效递送到细胞质中的通用策略。这些蛋白质具有一个寡(谷氨酸)序列(E 标签),可以与精氨酸功能化的金纳米颗粒结合,生成分级的球形纳米组装体。这些组装体与细胞膜融合,将 E 标记的蛋白质直接释放到细胞质中。五种不同的电荷、大小和功能的蛋白质被有效地递送到细胞中,证明了我们方法的通用性。重要的是,工程化蛋白质在细胞质递送后保持活性,通过递送活性 Cre 重组酶和 granzyme A 来杀死癌细胞得到了证明。