TY - JOUR
T1 - Filling Adeno-Associated Virus Capsids
T2 - Estimating Success by Cryo-Electron Microscopy
AU - Subramanian, Suriyasri
AU - Maurer, Anna C.
AU - Bator, Carol M.
AU - Makhov, Alexander M.
AU - Conway, James F.
AU - Turner, Kevin B.
AU - Marden, James H.
AU - Vandenberghe, Luk H.
AU - Hafenstein, Susan L.
N1 - Publisher Copyright:
© Copyright 2019, Mary Ann Liebert, Inc., publishers 2019.
PY - 2019/12
Y1 - 2019/12
N2 - Adeno-associated viruses (AAVs) have been employed successfully as gene therapy vectors in treating various genetic diseases for almost two decades. However, transgene packaging is usually imperfect, and developing a rapid and accurate method for measuring the proportion of DNA encapsidation is an important step for improving the downstream process of large scale vector production. In this study, we used two-dimensional class averages and three-dimensional classes, intermediate outputs in the single particle cryo-electron microscopy (cryo-EM) image reconstruction pipeline, to determine the proportion of DNA-packaged and empty capsid populations. Two different preparations of AAV3 were analyzed to estimate the minimum number of particles required to be sampled by cryo-EM in order for robust calculation of the proportion of the full versus empty capsids in any given sample. Cost analysis applied to the minimum amount of data required for a valid ratio suggests that cryo-EM is an effective approach to analyze vector preparations.
AB - Adeno-associated viruses (AAVs) have been employed successfully as gene therapy vectors in treating various genetic diseases for almost two decades. However, transgene packaging is usually imperfect, and developing a rapid and accurate method for measuring the proportion of DNA encapsidation is an important step for improving the downstream process of large scale vector production. In this study, we used two-dimensional class averages and three-dimensional classes, intermediate outputs in the single particle cryo-electron microscopy (cryo-EM) image reconstruction pipeline, to determine the proportion of DNA-packaged and empty capsid populations. Two different preparations of AAV3 were analyzed to estimate the minimum number of particles required to be sampled by cryo-EM in order for robust calculation of the proportion of the full versus empty capsids in any given sample. Cost analysis applied to the minimum amount of data required for a valid ratio suggests that cryo-EM is an effective approach to analyze vector preparations.
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U2 - 10.1089/hum.2019.041
DO - 10.1089/hum.2019.041
M3 - Article
C2 - 31530236
AN - SCOPUS:85077016381
SN - 1043-0342
VL - 30
SP - 1449
EP - 1460
JO - Human Gene Therapy
JF - Human Gene Therapy
IS - 12
ER -