Lam Anh K, Zhang Junping, Frabutt Dylan, Mulcrone Patrick L, Li Lei, Zeng Lifan, Herzog Roland W, Xiao Weidong
Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Department of Chemistry, Georgia State University, Atlanta, GA 30302, USA.
Mol Ther Methods Clin Dev. 2022 Sep 24;27:185-194. doi: 10.1016/j.omtm.2022.09.008. eCollection 2022 Dec 8.
Adeno-associated virus (AAV) has emerged as a leading platform for gene therapy. With the skyrocketing rate of AAV research and the prevalence of many new engineered capsids being investigated in preclinical and clinical trials, capsid characterization plays a vital role in serotype confirmation and quality control. Further, peptide mapping the capsid proteins might inevitably be a future requirement by regulatory agencies since it is a critical step in good manufacturing practice (GMP) for biotherapeutic characterization. To overcome many challenges that traditional methods like SDS-PAGE and western blots carry, liquid chromatography and mass spectrometry (LC-MS) allows high resolution and sensitivity with great accuracy in characterizing the AAV capsid proteins. Our optimized LC-MS method provides quick sample preparation, a fast and high-throughput 4-min run, and high sensitivity, which allows for very efficient characterization of wild-type and engineered capsids. This study also reports the usage of LC-MS/MS peptide mapping of AAV capsid proteins to determine the most accessible lysine residues targeted by chemical modifications. Our detailed protocols are anticipated to promote the development and discovery of AAV variants with high accuracy and efficiency.
腺相关病毒(AAV)已成为基因治疗的主要平台。随着AAV研究的飞速发展以及许多新型工程衣壳在临床前和临床试验中被研究,衣壳表征在血清型确认和质量控制中起着至关重要的作用。此外,对衣壳蛋白进行肽图谱分析可能不可避免地成为监管机构未来的要求,因为这是生物治疗表征的良好生产规范(GMP)中的关键步骤。为了克服SDS-PAGE和western印迹等传统方法所带来的诸多挑战,液相色谱和质谱联用(LC-MS)在表征AAV衣壳蛋白时具有高分辨率、高灵敏度和高精度的特点。我们优化的LC-MS方法提供了快速的样品制备、4分钟快速高通量运行以及高灵敏度,能够非常高效地表征野生型和工程衣壳。本研究还报告了使用LC-MS/MS对AAV衣壳蛋白进行肽图谱分析,以确定化学修饰靶向的最易接近的赖氨酸残基。我们详细的方案有望促进高精度和高效率的AAV变体的开发与发现。