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光化学内化(PCI)——一种从内吞小泡释放大分子的新技术。

Photochemical internalization (PCI)--a novel technology for release of macromolecules from endocytic vesicles.

作者信息

Berg Kristian, Prasmickaite Lina, Selbo Pål Kristian, Hellum Marit, Bonsted Anette, Høgset Anders

机构信息

Department of Biophysics, Institute for Cancer Research, Norwegian Radium Hospital, Montebello, N-0310 Oslo, Norway.

出版信息

Oftalmologia. 2003;56(1):67-71.

Abstract

The utilisation of macromolecules in therapy of cancer and other diseases is becoming increasingly relevant. Recent advances in molecular biology and biotechnology have made it possible to improve targeting and design of cytotoxic agents or DNA complexes for clinical applications. To achieve the expected biological effect of these macromolecules in many cases internalization to the cell cytosol is crucial. A number of different methods for internalization of membrane impermeable molecules has been established, including electroporation, liposome fusion, antibodies/targeting ligands as protein carriers and the utilisation of various types of vectors such as cationic polymers and viruses, for gene therapy. Although new delivery systems have improved the cellular uptake of macromolecules, tissue penetration, cellular uptake and efficient transfer of the molecules into the cytosol of the target cell are still fundamental obstacles. At an intracellular level, the most fundamental obstruction for cytosolic release of the therapeutic molecule is the membrane-barrier of the endocytic vesicles. Photochemical internalization (PCI) is a novel technology for release of endocytosed macromolecules into the cytosol. The technology is based on the use of photosensitizers located in endocytic vesicles that upon activation by light induce a release of macromolecules from their compartmentalization in endocytic vesicles. PCI has been shown to potentiate the biological activity of a large variety of macromolecules and other molecules that do not readily penetrate the plasma membrane, including proteins, peptides, and DNA delivered as a complex with cationic polymers or incorporated in adenovirus. The basis as well as the utilization of this technology will be briefly reviewed in this paper.

摘要

大分子在癌症及其他疾病治疗中的应用正变得越来越重要。分子生物学和生物技术的最新进展使得改进细胞毒性药物或DNA复合物的靶向性及设计以用于临床应用成为可能。在许多情况下,要实现这些大分子预期的生物学效应,其内化进入细胞胞质溶胶至关重要。已经建立了多种使膜不可渗透分子内化的不同方法,包括电穿孔、脂质体融合、作为蛋白质载体的抗体/靶向配体以及利用各种类型的载体(如阳离子聚合物和病毒)进行基因治疗。尽管新的递送系统改善了大分子的细胞摄取,但组织穿透、细胞摄取以及分子有效转移到靶细胞的胞质溶胶中仍然是基本障碍。在细胞内水平,治疗性分子胞质溶胶释放的最根本障碍是内吞小泡的膜屏障。光化学内化(PCI)是一种将内吞的大分子释放到胞质溶胶中的新技术。该技术基于使用位于内吞小泡中的光敏剂,其在光激活后诱导大分子从它们在内吞小泡中的分隔状态释放出来。PCI已被证明可增强多种不易穿透质膜的大分子和其他分子的生物活性,包括蛋白质、肽以及与阳离子聚合物复合或掺入腺病毒中递送的DNA。本文将简要综述该技术的基础及其应用。

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