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通过基于胶束纳米载体的非内吞摄取将蛋白质递送至细胞质和细胞核。

Protein Delivery to the Cytosol and Cell Nucleus via Micellar Nanocarrier-Based Nonendocytic Uptake.

作者信息

Shaw Santanu, Sarkar Ankan Kumar, Jana Nikhil R

机构信息

School of Materials Science, Indian Association for the Cultivation of Science, 2A & 2B Raja S. C. Mullick Road, Kolkata700032, India.

出版信息

ACS Appl Bio Mater. 2023 Oct 16;6(10):4200-4207. doi: 10.1021/acsabm.3c00431. Epub 2023 Sep 15.

Abstract

Although efficient cell nucleus delivery of exogenous materials can greatly improve their biochemical activity, this is strictly restricted by cellular uptake and intracellular trafficking processes. In the current approach, synthetic carriers are designed for cell delivery of exogenous materials via endocytosis, and nucleus delivery can be achieved via endosomal escape. Here, we demonstrate that a nonendocytic cell uptake approach can be adapted for protein delivery to the cell nucleus. We have designed a phenylboronic acid-terminated micellar carrier that can bind with protein in the presence of green tea polyphenol and deliver protein into the cytosol via the nonendocytic approach. Using this approach, four different proteins are delivered to the cytosol within 15 min, and low-molecular weight proteins are delivered to the nucleus. The designed approach can be extended for delivering macromolecular drugs to subcellular targets for a more efficient therapy.

摘要

尽管外源性物质的高效细胞核递送能极大地提高其生化活性,但这受到细胞摄取和细胞内运输过程的严格限制。在目前的方法中,合成载体被设计用于通过内吞作用将外源性物质递送至细胞,而细胞核递送可通过内体逃逸实现。在此,我们证明了一种非内吞性细胞摄取方法可适用于将蛋白质递送至细胞核。我们设计了一种以苯硼酸为末端的胶束载体,其在绿茶多酚存在下可与蛋白质结合,并通过非内吞方法将蛋白质递送至细胞质。使用这种方法,四种不同的蛋白质可在15分钟内递送至细胞质,低分子量蛋白质则可递送至细胞核。所设计的方法可扩展用于将大分子药物递送至亚细胞靶点,以实现更有效的治疗。

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