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天花粉蛋白:六十年的核糖体失活蛋白研究与开发。

A Sixty-Year Research and Development of Trichosanthin, a Ribosome-Inactivating Protein.

机构信息

Centre for Protein Science and Crystallography, School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong, China.

Li Dak Sum Yip Yio Chin R&D Centre for Chinese Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong, China.

出版信息

Toxins (Basel). 2022 Feb 27;14(3):178. doi: 10.3390/toxins14030178.

Abstract

Tian Hua Fen, a herbal powder extract that contains trichosanthin (TCS), was used as an abortifacient in traditional Chinese medicine. In 1972, TCS was purified to alleviate the side effects. Because of its clinical applications, TCS became one of the most active research areas in the 1960s to the 1980s in China. These include obtaining the sequence information in the 1980s and the crystal structure in 1995. The replication block of TCS on human immunodeficiency virus in lymphocytes and macrophages was found in 1989 and started a new chapter of its development. Clinical studies were subsequently conducted. TCS was also found to have the potential for gastric and colorectal cancer treatment. Studies on its mechanism showed TCS acts as an rRNA -glycosylase (EC 3.2.2.22) by hydrolyzing and depurinating A-4324 in α-sarcin/ricin loop on 28S rRNA of rat ribosome. Its interaction with acidic ribosomal stalk proteins was revealed in 2007, and its trafficking in mammalian cells was elucidated in the 2000s. The adverse drug reactions, such as inducing immune responses, short plasma half-life, and non-specificity, somehow became the obstacles to its usage. Immunotoxins, sequence modification, or coupling with polyethylene glycerol and dextran were developed to improve the pharmacological properties. TCS has nicely shown the scientific basis of traditional Chinese medicine and how its research and development have expanded the knowledge and applications of ribosome-inactivating proteins.

摘要

天花粉,一种含有天花粉蛋白(TCS)的草药粉提取物,曾在中国传统医学中被用作堕胎药。1972 年,TCS 被纯化以减轻其副作用。由于其临床应用,TCS 成为 20 世纪 60 年代至 80 年代中国最活跃的研究领域之一。其中包括在 20 世纪 80 年代获得序列信息和 1995 年获得晶体结构。1989 年发现 TCS 在淋巴细胞和巨噬细胞上对人类免疫缺陷病毒的复制阻断作用,开启了其发展的新篇章。随后进行了临床研究。TCS 也被发现具有治疗胃癌和结直肠癌的潜力。对其机制的研究表明,TCS 通过水解和脱嘌呤 A-4324 在大鼠核糖体 28S rRNA 的α-鹅膏蕈碱/蓖麻毒素环上作为 rRNA-糖苷酶(EC 3.2.2.22)发挥作用。2007 年揭示了其与酸性核糖体柄蛋白的相互作用,2000 年代阐明了其在哺乳动物细胞中的运输。诱导免疫反应、血浆半衰期短和非特异性等不良反应在一定程度上成为其应用的障碍。免疫毒素、序列修饰或与聚乙二醇和葡聚糖偶联被开发用于改善药理学特性。TCS 很好地展示了中药的科学基础,以及其研究和开发如何扩展核糖体失活蛋白的知识和应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39ba/8950148/d66a18bf4824/toxins-14-00178-g001.jpg

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