Selective Enrichment of Full AAV Capsids

TL;DR

This paper introduces a novel, efficient, and scalable one-step crystallization method to selectively enrich full AAV capsids from mixtures, significantly improving yield and purity while reducing processing time and costs.

Contribution

The study demonstrates the first use of selective crystallization for separating full AAV capsids without chemical modification, enhancing purity and yield in a single step.

Findings

Achieved over 80% full capsid enrichment

Increased yield by approximately 30%

Reduced processing time by about 87%

Abstract

Gene therapies using recombinant adeno-associated virus (rAAV) have been developed to treat monogenic and acquired diseases but are currently the most expensive drugs due, in part, to high manufacturing costs. The cells producing rAAV generate substantial quantities of empty (50-90%) and partially filled capsids that must be removed prior to final formulation. The conventional separation processes are inefficient in removing empty and partially filled capsids, have low yield, scale poorly, time consuming and need additional purification steps. This article demonstrates one step separation of full capsids from a mixture of full, partially filled, and empty capsids, and other protein impurities using selective crystallization, a purification process, which is first time in protein purification and is performed without physically or chemically modifying the target component for the first time in the history of selective crystallization, and is highly-efficient, highly-scalable, and economical. Hanging-drop vapor diffusion experiments were used to scout crystallization conditions in which full and empty capsids crystallize, then to define conditions in which crystals of full, empty, or both full and empty capsids nucleate and grow. The experimental results for rAAV serotypes 5, 8, and 9 as exemplary vectors and scale-up results show that full capsids can be selectively crystallized and separated in one step from a mixture of full, partially filled, and empty capsids, and other proteins with full capsid enrichment of greater than 80%, approximately 20% higher, and yield of greater than 90%, approximately greater than 30% higher from the existing methods, keeping their biological activity intact, in a short period of time (less than 4 h), with approximately 87% reduction in processing time from the existing processing time and without the need of additional purification steps and in one round.