Choice of fusion proteins, expression host, and analytics solves difficult-to-produce protein challenges in discovery research

被引:1
|
作者
Lyons-Abbott, Sally [1 ]
Abramov, Ariel [1 ]
Chan, Chung-leung [1 ]
Deer, Jen Running [1 ]
Fu, Guangsen [1 ]
Hassouneh, Wafa [1 ]
Koch, Tyree [1 ]
Misquith, Ayesha [1 ]
O'Neill, Jason [1 ]
Simon, Sandy Alexander [1 ]
Wolf, Anitra [1 ]
Yeh, Ronald [1 ]
Vernet, Erik [1 ,2 ]
机构
[1] Novo Nordisk Res Ctr Seattle Inc, Seattle, WA USA
[2] Novo Nordisk Res Ctr Seattle Inc, Seattle, WA 98109 USA
关键词
protein engineering; protein expression; protein purification; recombinant proteins; ESCHERICHIA-COLI; PURIFICATION; ISOMERASE; PIPELINE; PARTNERS; TAGS;
D O I
10.1002/biot.202300162
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein-based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mammalian and bacterial hosts-91% of which are successfully expressed and purified-are discussed. Mammalian expression combined with the use of solubility-promoting fusion proteins is deemed suitable for most targets. Furthermore, cases utilizing stable cell line generation and choice of fusion protein for higher yield and quality of difficult-to-produce proteins (Leucine-rich repeat-containing G-protein coupled receptor 4 (LGR4) and Neurturin) are presented and discussed. In the case of Neurturin, choice of fusion protein impacted the target binding 80-fold. These results highlight the need for exploration of construct designs and careful Quality Control (QC) of difficult-to-produce protein reagents. Over 2800 variants of over 250 different human proteins were expressed in bacterial and mammalian expression system. The highest success rate was found using large plasma proteins such as albumin as fusion proteins. The proteins were carefully characterized and stable cell line generated in a particular challenging case.image
引用
收藏
页数:11
相关论文
共 1 条
  • [1] Nanobody fusion enhances production of difficult-to-produce secretory proteins
    Yan, Runchuan
    Zhang, Yan
    Zhang, Hui
    Ma, Jiyan
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2025, 301 (03)