دورية أكاديمية

Computer-Aided Directed Evolution Generates Novel AAV Variants with High Transduction Efficiency.

التفاصيل البيبلوغرافية
العنوان: Computer-Aided Directed Evolution Generates Novel AAV Variants with High Transduction Efficiency.
المؤلفون: Han, Zengpeng, Luo, Nengsong, Wang, Fei, Cai, Yuxiang, Yang, Xin, Feng, Weiwei, Zhu, Zhenxiang, Wang, Jie, Wu, Yang, Ye, Chaohui, Lin, Kunzhang, Xu, Fuqiang
المصدر: Viruses (1999-4915); Apr2023, Vol. 15 Issue 4, p848, 14p
مصطلحات موضوعية: GENETIC transduction, ADENO-associated virus, CENTRAL nervous system, COMPUTER-aided engineering, GENE libraries
مستخلص: Adeno-associated viruses (AAVs) have become safe and effective tools for therapeutic in vivo gene drug delivery. Among many AAV serotypes, AAV2 is the most well-characterized. Although many studies have been carried out on the engineering of the capsid VR-VIII region, few attempts have been made in the VR-IV region. Here, we targeted amino acid positions 442–469 of the VR-IV region and established an engineering paradigm of computer-aided directed evolution, based on training samples from previous datasets, to obtain a viral vector library with high diversity (~95,089). We further examined two variants selected from the library. The transduction efficiency of these two novel AAV variants, AAV2.A1 and AAV2.A2, in the central nervous system was 10–15 times higher than that of AAV2. This finding provides new vehicles for delivering gene drugs to the brain. [ABSTRACT FROM AUTHOR]
Copyright of Viruses (1999-4915) is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:19994915
DOI:10.3390/v15040848