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细胞穿透肽作为肽、蛋白质和寡核苷酸递送的载体。

Cell-penetrating peptides as vectors for peptide, protein and oligonucleotide delivery.

作者信息

Mäe Maarja, Langel Ulo

机构信息

Department of Neurochemistry, Stockholm University, Svante Arrhenius väg 21A, SE-106 91 Stockholm, Sweden.

出版信息

Curr Opin Pharmacol. 2006 Oct;6(5):509-14. doi: 10.1016/j.coph.2006.04.004. Epub 2006 Jul 24.

Abstract

High molecular weight biomolecules are becoming more and more important in the development of new therapeutic drugs. However, the hydrophilic nature of such molecules creates a major limitation for their application--poor penetration through biological membranes. In 1994, a new class of peptides--cell-penetrating peptides (CPPs)--was discovered. CPPs seem to greatly facilitate the delivery of hydrophilic macromolecules over the plasma membrane, both in vitro and in vivo, and show promise for therapeutic purposes. One such example--suppressor of cytokine signalling 3 protein--was shown to act as an effective inhibitor of acute inflammation in vivo owing to its successful delivery by CPPs.

摘要

高分子量生物分子在新型治疗药物的开发中变得越来越重要。然而,这类分子的亲水性对其应用造成了一个主要限制——难以穿透生物膜。1994年,一类新的肽——细胞穿透肽(CPPs)——被发现。CPPs似乎极大地促进了亲水性大分子在体外和体内穿过质膜的传递,并显示出治疗应用的前景。一个这样的例子——细胞因子信号传导抑制因子3蛋白——由于通过CPPs成功递送,在体内被证明是急性炎症的有效抑制剂。

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