Xu Jianfeng, Kieliszewski Marcia J
Arkansas Biosciences Institute, Arkansas State University, State University, AR, USA.
Methods Mol Biol. 2012;824:483-500. doi: 10.1007/978-1-61779-433-9_26.
Plant cell suspension culture integrates the merits of whole-plant systems with those of microbial fermentation and mammalian cell culture, and has been recognized as a promising alternative biosynthetic platform for valuable proteins. However, the low protein productivity dilemma has been the bottleneck toward commercializing this technology. Here, we describe a new technology, termed hydroxyproline (Hyp)-Glyco technology, that dramatically increases the yield of secreted recombinant proteins from cultured plant cells by expressing them as fusions with a novel glycomodule tag comprising an Hyp-rich repetitive peptide (HypRP) backbone that is subsequently glycosylated through the Hyp residues. The extensive glycosylation of the HypRP tags greatly extends the serum half-life of small therapeutic proteins, such as interferon α2b or human growth hormone, without significantly impairing their bioactivities and the tag greatly enhances solubility.
植物细胞悬浮培养融合了全植物系统、微生物发酵和哺乳动物细胞培养的优点,已被公认为是一种有前景的用于生产有价值蛋白质的替代生物合成平台。然而,低蛋白生产率的困境一直是该技术商业化的瓶颈。在此,我们描述了一种新技术,称为羟脯氨酸(Hyp)-糖基化技术,该技术通过将分泌的重组蛋白表达为与一种新型糖基化模块标签的融合蛋白,显著提高了培养植物细胞中分泌型重组蛋白的产量,该标签包含富含Hyp的重复肽(HypRP)主链,随后通过Hyp残基进行糖基化。HypRP标签的广泛糖基化极大地延长了小型治疗性蛋白(如干扰素α2b或人生长激素)的血清半衰期,而不会显著损害其生物活性,并且该标签还大大提高了溶解度。