Accelerating and de-risking CMC development with transposon-derived manufacturing cell lines

被引:17
作者
Rajendran, Sowmya [1 ,2 ,3 ]
Balasubramanian, Sowmya [1 ,2 ,3 ]
Webster, Lynn [1 ,2 ,3 ]
Lee, Maggie [1 ,2 ,3 ]
Vavilala, Divya [1 ,2 ,3 ]
Kulikov, Nicolay [1 ,2 ,3 ]
Choi, Jessica [1 ,2 ,3 ]
Tang, Calvin [1 ,2 ,3 ]
Hunter, Molly [1 ,2 ,3 ]
Wang, Rebecca [1 ,2 ,3 ]
Kaur, Harpreet [1 ,2 ,3 ]
Karunakaran, Surya [1 ,2 ,3 ]
Sitaraman, Varsha [1 ,2 ,3 ]
Minshull, Jeremy [1 ,2 ,3 ]
Boldog, Ferenc [1 ,2 ,3 ]
机构
[1] ATUM Inc, Cell Line Dev Dept, 37950 Cent Ct, Newark, CA 94560 USA
[2] ATUM Inc, Prot Purificat Dept, 37950 Cent Ct, Newark, CA 94560 USA
[3] ATUM Inc, Prot Analyt Dept, 37950 Cent Ct, Newark, CA 94560 USA
关键词
cell line development; integration; Leap‐ In transposase; stable pools; transposase; transposon; CHO; GENERATION; IDENTIFICATION; PIGGYBAC;
D O I
10.1002/bit.27742
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of highly productive, genetically stable manufacturing cell lines is on the critical path to IND filing for protein-based biologic drugs. Here, we describe the Leap-In Transposase (R) platform, a novel transposon-based mammalian (e.g., Chinese hamster ovary) cell line development system that produces high-titer stable pools with productivity and product quality attributes that are highly comparable to clones that are subsequently derived therefrom. The productivity distributions of clones are strongly biased toward high producers, and genetic and expression stability is consistently high. By avoiding the poor integration rates, concatemer formation, detrimental transgene recombination, low average expression level, unpredictable product quality, and inconsistent genetic stability characteristic of nonhomologous recombination methods, Leap-In provides several opportunities to de-risk programs early and reduce timelines and resources.
引用
收藏
页码:2301 / 2311
页数:11
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