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牛肾上腺髓质毛细血管内皮细胞中甘露糖基磷酸多萜醇合酶的克隆与表达

Cloning and expression of mannosylphospho dolichol synthase from bovine adrenal medullary capillary endothelial cells.

作者信息

Baksi Krishna, Zhang Zhenbo, Banerjee Aditi, Banerjee Dipak K

机构信息

Department of Anatomy and Cell Biology, School of Medicine, Universidad Central del Caribe, Bayamón, PR 00930-3100, USA.

出版信息

Glycoconj J. 2009 Aug;26(6):635-45. doi: 10.1007/s10719-008-9214-9. Epub 2009 Feb 12.

Abstract

Mannosylphospho dolichol synthase (DPMS) is a critical enzyme in the biosynthesis of lipid-linked oligosaccharide (LLO; Glc(3)Man(9)GlcNAc(2)-PP-Dol), a pre-requisite for asparagine-linked (N-linked) protein glycosylation. We have shown earlier that DPMS is important for angiogenesis, i.e., endothelial cell proliferation. This is true when cAMP is used for intracellular signaling. During cAMP signaling, DPMS is activated and ER stress is reduced. To understand the activation of DPMS at the molecular level we have isolated a cDNA clone for the DPMS gene (bDPMS) from the capillary endothelial cells of bovine adrenal medulla. DNA sequencing and the deduced amino acid sequence have established that bDPMS has a motif to be phosphorylated by cAMP-dependent protein kinase (PKA). Based on the sequence information Serine 165 has been found to be the phosphorylation target in bDPMS. Hydropathy Index when plotted against amino acid number indicates the presence of a hydrophobic region around the amino acid residues 120-160, supporting that bDPMS has one membrane spanning region. The recombinant bDPMS has now been purified as His-tag protein with an apparent molecular weight of M (r) 33 kDa. Additionally, we show here that overexpression of DPMS is indeed angiogenic. The capillary endothelial cells proliferate at a higher rate carrying the DPMS overexpression plasmid over the parental cells or the vector.

摘要

甘露糖基磷酸多萜醇合酶(DPMS)是脂质连接寡糖(LLO;Glc(3)Man(9)GlcNAc(2)-PP-Dol)生物合成中的关键酶,而LLO是天冬酰胺连接(N连接)蛋白糖基化的前提条件。我们之前已经表明DPMS对血管生成很重要,即对内皮细胞增殖很重要。当使用cAMP进行细胞内信号传导时就是如此。在cAMP信号传导过程中,DPMS被激活,内质网应激减轻。为了在分子水平上理解DPMS的激活机制,我们从牛肾上腺髓质的毛细血管内皮细胞中分离出了DPMS基因的cDNA克隆(bDPMS)。DNA测序和推导的氨基酸序列表明,bDPMS具有一个可被cAMP依赖性蛋白激酶(PKA)磷酸化的基序。根据序列信息,已发现丝氨酸165是bDPMS中的磷酸化靶点。将亲水性指数与氨基酸数量作图表明,在氨基酸残基120 - 160周围存在一个疏水区,这支持bDPMS具有一个跨膜区。重组bDPMS现已作为His标签蛋白纯化,其表观分子量为M(r)33 kDa。此外,我们在此表明DPMS的过表达确实具有血管生成作用。携带DPMS过表达质粒的毛细血管内皮细胞比亲代细胞或载体细胞以更高的速率增殖。

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