衣壳
腺相关病毒
等电聚焦
转导(生物物理学)
遗传增强
转基因
生物
体外
血清型
基因
分子生物学
病毒
重组DNA
化学
病毒学
生物物理学
遗传学
生物化学
载体(分子生物学)
酶
作者
Brandon Hoyle,Dhimiter Bello,Jonathan Hill,Soumita Das,Jonghan Kim
标识
DOI:10.2174/0115665232369708250327081305
摘要
OBJECTIVE: Adeno-Associated Virus (AAV) vectors are comprised of a capsid protein encapsulating a Deoxyribonucleic Acid (DNA) transgene that has been used in the gene therapy field showing potential to treat a range of genetic diseases. Methods in the field of gene therapy should be optimized or enhanced to deepen understanding of AAVs, specifically around charge heterogeneity of capsid species. METHODS: In this study, a versatile approach was presented for investigating the charge heterogeneity of AAV capsid proteins of a variety of serotypes. This method employs Imaged Capillary Isoelectric Focusing (icIEF) coupled with native fluorescence imaging detection and has undergone exhaustive validation. RESULTS: Demonstrating its platform nature, this method analyzed seven different AAV serotypes from multiple manufacturing platforms. The distinctive profiles generated for each AAV serotype serve as valuable indicators for both identity confirmation and stability assessment. It was shown that thermal stress and pH conditions play a role in increasing acidic charged variants over time, affecting the charge heterogeneity of AAVs, which can be serotype-specific. Reverse phase LC-MS was used to identify and confirm the increased presence of Post-Translational Modifications (PTMs) that are linked to increasing acidic species variants relative to non-stressed AAVs. CONCLUSION: potency.
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