Degradation and stable maintenance of adeno-associated virus inverted terminal repeats in E. coli

被引:0
|
作者
Radukic, Marco T. [1 ]
Le, Dinh To [1 ,3 ]
Krassuski, Timo [1 ]
Borchert, Philipp [1 ]
Leach, David R. F. [2 ]
Mueller, Kristian M. [1 ]
机构
[1] Bielefeld Univ, Fac Technol, Cellular & Mol Biotechnol, Univ Str 25, D-33615 Bielefeld, North Rhine Wes, Germany
[2] Univ Edinburgh, Inst Cell Biol, Sch Biol Sci, Kings Bldg,Mayfield Rd, Edinburgh EH9 3BF, Scotland
[3] Univ Med Ctr Hamburg Eppendorf, Dept Med, D-20246 Hamburg, Germany
关键词
ESCHERICHIA-COLI; RECOMBINANT PLASMID; DNA HAIRPINS; PALINDROME; REPLICATION; GENE; MECHANISM; DELETION; RESCUE;
D O I
10.1093/nar/gkae1170
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current plasmid propagation in E. coli compromises large inverted repeats, such as inverted terminal repeats (ITRs) of adeno-associated virus (AAV). Direct long-read sequencing analyses upon varying strains and culture conditions revealed ITR instability caused by a slipped misalignment mechanism, although other mechanism probably contribute. ITRs stabilized in absence of SbcC, which is part of the SbcCD nuclease complex, a human Mre11-Rad50 homolog, or at elevated growth temperatures (e.g. 42 degrees C), with a combination being optimal. Resulting full ITR transgene plasmids improved rAAV yield and purity in HEK-293 productions. The findings advance plasmid biology, cloneable sequences and therapeutic AAV manufacturing.
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页数:6
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