首页> 外文期刊>Glycoconjugate journal >Mannose-6-phosphate receptors (MPR 300 and 46) from the highly evolved invertebrate Asterias rubens (Echinodermate): biochemical and functional characterization of MPR 46 protein
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Mannose-6-phosphate receptors (MPR 300 and 46) from the highly evolved invertebrate Asterias rubens (Echinodermate): biochemical and functional characterization of MPR 46 protein

机译:高度进化的无脊椎动物红豆(Echinodermate)的6-磷酸甘露糖受体(MPR 300和46):MPR 46蛋白的生化和功能表征

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摘要

Mammalian mannose 6-phosphate receptors (MPR 300 and 46) mediate transport of lysosomal enzymes to lysosomes. Recent studies established that the receptors are conserved throughout vertebrates. Although we purified the mollusc receptors and identified only a lysosomal enzyme receptor protein (LERP) in the Drosophila melanogaster, little is known about their structure and functional roles in the invertebrates. In the present study, we purified the putative receptors from the highly evolved invertebrate, starfish, cloned the cDNA for the MPR 46, and expressed it in mpr(-/-) mouse embryonic fibroblast cells. Structural comparison of starfish receptor sequences with other vertebrate receptors gave valuable information on its extensive structural homology with the vertebrate MPR 46 proteins. The expressed protein efficiently sorts lysosomal enzymes within the cells establishing a functional role for this protein. This first report on the invertebrate MPR 46 further confirms the structural and functional conservation of the receptor not only in the vertebrates but also in the invertebrates.
机译:哺乳动物甘露糖6-磷酸受体(MPR 300和46)介导溶酶体酶向溶酶体的转运。最近的研究表明,受体在整个脊椎动物中都是保守的。尽管我们纯化了软体动物受体,并在果蝇中仅鉴定了溶酶体酶受体蛋白(LERP),但对其在无脊椎动物中的结构和功能作用知之甚少。在本研究中,我们从高度进化的无脊椎动物海星中纯化了假定的受体,克隆了MPR 46的cDNA,并在mpr(-/-)小鼠胚胎成纤维细胞中表达了它。海星受体序列与其他脊椎动物受体的结构比较提供了有关其与脊椎动物MPR 46蛋白广泛的结构同源性的有价值的信息。表达的蛋白质有效地分选了细胞内的溶酶体酶,从而建立了该蛋白质的功能性角色。关于无脊椎动物MPR 46的第一份报告进一步证实了受体的结构和功能保守性不仅在脊椎动物中,而且在无脊椎动物中也是如此。

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