Rosenkranz Andrey A, Slastnikova Tatiana A
Laboratory of Molecular Genetics of Intracellular Transport, Institute of Gene Biology of Russian Academy of Sciences, 34/5 Vavilov St., 119334 Moscow, Russia.
Department of Biophysics, Faculty of Biology, Lomonosov Moscow State University, 1-12 Leninskie Gory St., 119234 Moscow, Russia.
Pharmaceutics. 2023 Mar 19;15(3):987. doi: 10.3390/pharmaceutics15030987.
A large number of proteins are successfully used to treat various diseases. These include natural polypeptide hormones, their synthetic analogues, antibodies, antibody mimetics, enzymes, and other drugs based on them. Many of them are demanded in clinical settings and commercially successful, mainly for cancer treatment. The targets for most of the aforementioned drugs are located at the cell surface. Meanwhile, the vast majority of therapeutic targets, which are usually regulatory macromolecules, are located inside the cell. Traditional low molecular weight drugs freely penetrate all cells, causing side effects in non-target cells. In addition, it is often difficult to elaborate a small molecule that can specifically affect protein interactions. Modern technologies make it possible to obtain proteins capable of interacting with almost any target. However, proteins, like other macromolecules, cannot, as a rule, freely penetrate into the desired cellular compartment. Recent studies allow us to design multifunctional proteins that solve these problems. This review considers the scope of application of such artificial constructs for the targeted delivery of both protein-based and traditional low molecular weight drugs, the obstacles met on the way of their transport to the specified intracellular compartment of the target cells after their systemic bloodstream administration, and the means to overcome those difficulties.
大量蛋白质已成功用于治疗各种疾病。这些包括天然多肽激素、其合成类似物、抗体、抗体模拟物、酶以及基于它们的其他药物。其中许多在临床环境中很受欢迎且商业上很成功,主要用于癌症治疗。上述大多数药物的靶点位于细胞表面。与此同时,绝大多数治疗靶点,通常是调节性大分子,位于细胞内部。传统的低分子量药物可自由穿透所有细胞,在非靶细胞中产生副作用。此外,通常很难精心设计出一种能特异性影响蛋白质相互作用的小分子。现代技术使获得能够与几乎任何靶点相互作用的蛋白质成为可能。然而,蛋白质与其他大分子一样,通常不能自由穿透到所需的细胞区室中。最近的研究使我们能够设计出解决这些问题的多功能蛋白质。本文综述了此类人工构建体在基于蛋白质的药物和传统低分子量药物靶向递送方面的应用范围、它们在全身血液循环给药后运输到靶细胞特定细胞内区室过程中遇到的障碍以及克服这些困难的方法。