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1、2和5型重组腺相关病毒载体的生产与纯化

Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors.

作者信息

Zolotukhin Sergei, Potter Mark, Zolotukhin Irene, Sakai Yoshihisa, Loiler Scott, Fraites Thomas J, Chiodo Vince A, Phillipsberg Tina, Muzyczka Nicholas, Hauswirth William W, Flotte Terance R, Byrne Barry J, Snyder Richard O

机构信息

Powell Gene Therapy Center, 1600 SW Archer Road, College of Medicine, University of Florida, 32610-0266, Gainesville, FL 32610-0266, USA.

出版信息

Methods. 2002 Oct;28(2):158-67. doi: 10.1016/s1046-2023(02)00220-7.

Abstract

Recombinant adeno-associated viral (rAAV) vectors based on serotype 2 are currently being evaluated most extensively in animals and human clinical trials. rAAV vectors constructed from other AAV serotypes (serotypes 1, 3, 4, 5, and 6) can transduce certain tissues more efficiently and with different specificity than rAAV2 vectors in animal models. Here, we describe reagents and methods for the production and purification of AAV2 inverted terminal repeat-containing vectors pseudotyped with AAV1 or AAV5 capsids. To facilitate pseudotyping, AAV2rep/AAV1cap and AAV2rep/AAV5cap helper plasmids were constructed in an adenoviral plasmid backbone. The resultant plasmids, pXYZ1 and pXYZ5, were used to produce rAAV1 and rAAV5 vectors, respectively, by transient transfection. Since neither AAV5 nor AAV1 binds to the heparin affinity chromatography resin used to purify rAAV2 vectors, purification protocols were developed based on anion-exchange chromatography. The purified vector stocks are 99% pure with titers of 1 x 10(12) to 1 x 10(13)vector genomes/ml.

摘要

基于2型血清型的重组腺相关病毒(rAAV)载体目前正在动物和人体临床试验中得到最广泛的评估。在动物模型中,由其他AAV血清型(血清型1、3、4、5和6)构建的rAAV载体比rAAV2载体能更有效地转导某些组织,且具有不同的特异性。在此,我们描述了用AAV1或AAV5衣壳假型化的含AAV2反向末端重复序列载体的生产和纯化试剂及方法。为便于假型化,在腺病毒质粒骨架中构建了AAV2rep/AAV1cap和AAV2rep/AAV5cap辅助质粒。所得质粒pXYZ1和pXYZ5分别用于通过瞬时转染生产rAAV1和rAAV5载体。由于AAV5和AAV1均不与用于纯化rAAV2载体的肝素亲和层析树脂结合,因此基于阴离子交换层析开发了纯化方案。纯化后的载体原液纯度为99%,滴度为1×10¹²至1×10¹³载体基因组/毫升。

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