药物输送
表位
病毒
类病毒颗粒
抗原
病毒学
免疫系统
药品
计算生物学
基因工程
纳米技术
生物
化学
材料科学
重组DNA
免疫学
生物化学
基因
药理学
作者
Brett Hill,Andrew J. Zak,Eshita Khera,Fei Wen
出处
期刊:Current Protein & Peptide Science
[Bentham Science]
日期:2017-11-21
卷期号:19 (1): 112-127
被引量:73
标识
DOI:10.2174/1389203718666161122113041
摘要
Virus-like particles (VLPs) are nanoscale biological structures consisting of viral proteins assembled in a morphology that mimic the native virion but do not contain the viral genetic material. The possibility of chemically and genetically modifying the proteins contained within VLPs makes them an attractive system for numerous applications. As viruses are potent immune activators as well as natural delivery vehicles of genetic materials to their host cells, VLPs are especially well suited for antigen and drug delivery applications. Despite the great potential, very few VLP designs have made it through clinical trials. In this review, we will discuss the challenges of developing VLPs for antigen and drug delivery, strategies being explored to address these challenges, and the genetic and chemical approaches available for VLP engineering.
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