化学
色谱法
腺相关病毒
肽
血清型
亲和层析
病毒学
生物化学
重组DNA
酶
载体(分子生物学)
基因
生物
作者
Shriarjun Shastry,Eduardo Barbieri,Arianna Minzoni,Wenning Chu,Stephanie N. Johnson,Mark Stoops,Jennifer Pancorbo,Gary Gilleskie,Steven R. Meshnick,Michael Crapanzano,Michael A. Daniele,Stefano Menegatti
标识
DOI:10.1016/j.chroma.2024.465320
摘要
Adeno-associated viruses (AAVs) have emerged as a prominent family of vectors for gene delivery, providing therapeutic options to diseases once deemed incurable. At the same time, they necessitate efficient and affordable purification methods that can be platformed to serve all AAV serotypes. Current chromatographic tools, while affording high product purity, fail to bind certain serotypes, provide limited yield and lifetime, and impose harsh elution conditions that can compromise the vector's activity and safety. Addressing these challenges, this work demonstrates the application of new peptide ligands as the first serotype-agnostic technology for AAV purification by affinity chromatography. Our study reveals a pH-dependent affinity interaction: AAV2, AAV3, AAV6, AAV9, and AAVrh.10 are effectively captured at neutral pH, while binding AAV1, AAV5, AAV7, and AAV8 is stronger in a slightly acidic environment. The elution of bound AAVs was achieved using magnesium chloride at neutral pH for all serotypes, consistently affording capsid yields above 50% and genome yields above 80%, together with a >100-fold reduction in host cell proteins and nucleic acids. In particular, peptide ligand A10 exhibited remarkable binding capacity (> 10
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