Production of functional human insulin-like growth factor binding proteins (IGFBPs) using recombinant expression in HEK293 cells

被引:4
作者
Wanscher, Anne Sofie Molsted [1 ]
Williamson, Michael [2 ]
Ebersole, Tasja Wainani [2 ]
Streicher, Werner [1 ,3 ]
Wikstrom, Mats [1 ]
Cazzamali, Giuseppe [2 ]
机构
[1] Univ Copenhagen, Ctr Prot Res, Novo Nordisk Fdn, Prot Funct & Interact Grp, DK-1168 Copenhagen, Denmark
[2] Univ Copenhagen, Ctr Prot Res, Novo Nordisk Fdn, Prot Prod & Characterizat Platform, DK-1168 Copenhagen, Denmark
[3] Novozymes AS, Bagsvaerd, Denmark
关键词
Recombinant full-length human IGFBP; HEK293; cells; Secretory expression; Post-translational modification; Surface plasmon resonance; A PAPP-A; TERMINAL FRAGMENTS; I RECEPTOR; PLASMA; GLYCOSYLATION; TRANSFECTION; PROTEOLYSIS; PEPTIDES; DOMAIN; MAC25;
D O I
10.1016/j.pep.2014.10.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Insulin-like growth factor binding proteins (IGFBPs) display many functions in humans including regulation of the insulin-like growth factor (IGF) signaling pathway. The various roles of human IGFBPs make them attractive protein candidates in drug discovery. Structural and functional knowledge on human proteins with therapeutic relevance is needed to design and process the next generation of protein therapeutics. In order to conduct structural and functional investigations large quantities of recombinant proteins are needed. However, finding a suitable recombinant production system for proteins such as full-length human IGFBPs, still remains a challenge. Here we present a mammalian HEK293 expression method suitable for over-expression of secretory full-length human IGFBP-1 to -7. Protein purification of full-length human IGFBP-1, -2, -3 and -5 was conducted using a two-step chromatography procedure and the final protein yields were between 1 and 12 mg protein per liter culture media. The recombinant IGFBPs contained PTMs and exhibited high-affinity interactions with their natural ligands IGF-1 and IGF-2. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:97 / 105
页数:9
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