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用于抗病毒药物开发的细胞穿透肽

Cell-Penetrating Peptides for Antiviral Drug Development.

作者信息

Delcroix Melaine, Riley Lee W

机构信息

School of Public Health, University of California, Berkeley, CA 94720, USA.

出版信息

Pharmaceuticals (Basel). 2010 Mar 2;3(3):448-470. doi: 10.3390/ph3030448.

Abstract

Viral diseases affect hundreds of millions of people worldwide, and the few available drugs to treat these diseases often come with limitations. The key obstacle to the development of new antiviral agents is their delivery into infected cells . Cell-penetrating peptides (CPPs) are short peptides that can cross the cellular lipid bilayer with the remarkable capability to shuttle conjugated cargoes into cells. CPPs have been successfully utilized to enhance the cellular uptake and intracellular trafficking of antiviral molecules, and thereby increase the inhibitory activity of potential antiviral proteins and oligonucleotide analogues, both in cultured cells and in animal models. This review will address the notable findings of these studies, highlighting some promising results and discussing the challenges CPP technology has to overcome for further clinical applications.

摘要

病毒性疾病影响着全球数亿人,而治疗这些疾病的可用药物往往存在局限性。开发新型抗病毒药物的关键障碍在于将其递送至受感染细胞。细胞穿透肽(CPPs)是短肽,能够穿过细胞脂质双层,具有将共轭货物转运到细胞内的显著能力。CPPs已成功用于增强抗病毒分子的细胞摄取和细胞内运输,从而提高潜在抗病毒蛋白和寡核苷酸类似物在培养细胞和动物模型中的抑制活性。本综述将阐述这些研究的显著发现,突出一些有前景的结果,并讨论CPP技术在进一步临床应用中必须克服的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d404/4033964/9ee459eb8c3e/pharmaceuticals-03-00448-g001.jpg

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