Probe capsid structure stability and dynamics of adeno‐associated virus as an important viral vector for gene therapy by hydrogen‐deuterium exchange‐mass spectrometry

Abstract

AbstractAdeno‐associated virus (AAV), a widely used gene therapy vector, is a small, nonenveloped virus that contains a single‐stranded DNA genome with a maximum length of 4.7 kb. Despite extensive biophysical and structural characterization, many aspects of AAV functions remain elusive. This knowledge gap is primarily due to a lack of structurally resolved dynamic information and the absence of structural coverage of functionally critical segments on the AAV capsid. Here, we developed a protocol to study AAV structural dynamics by hydrogen‐deuterium exchange mass spectrometry (HDX‐MS), a powerful method for monitoring protein structure stability and dynamics in solution. We performed HDX‐MS measurements on AAVs without or with different DNA payloads of different sizes, and obtained detailed dynamic information on the entire AAV sequence including the two functionally important segments not previously structurally characterized. The unique N terminus of the capsid protein VP1 (VP1u) was found to adopt a highly dynamic and unstable conformation with low HDX protection across the entire region, whereas the presence of a DNA payload increased its protection. The VP1 and VP2 shared region (VP1/2) showed no measurable protection, with or without DNA. Differential HDX between empty and full capsid samples allowed us to identify potential new DNA‐capsid interaction sites located primarily around the five‐fold channel, which differ from the three‐fold pocket binding site previously identified. Our HDX‐MS method for characterizing AAV structural dynamics opens a new way for future efforts to understand AAV structure–function relationships and engineer next‐generation AAV vectors with improved gene delivery properties.