Suppr超能文献

金头鲷(Sparus auratus)重组甲状旁腺激素相关蛋白的制备与表征

Production and characterisation of gilthead sea bream (Sparus auratus) recombinant parathyroid hormone related protein.

作者信息

Anjos L, Rotllant J, Guerreiro P M, Hang X, Canario A V M, Balment R, Power D M

机构信息

Comparative and Molecular Endocrinology Group, CCMAR, CIMAR-Laboratório Associado, Universidade do Algarve, Campus de Gambelas, 8005-139 Faro, Portugal.

出版信息

Gen Comp Endocrinol. 2005 Aug;143(1):57-65. doi: 10.1016/j.ygcen.2005.02.020. Epub 2005 Apr 2.

Abstract

The production and purification of gilthead sea bream recombinant parathyroid hormone related protein [sbPTHrP(1-125)] using an Escherichia coli system and one step purification process with continuous elution gel electrophoresis is reported. The cDNA encoding sbPTHrP(1-125) was cloned into a prokaryotic expression vector pET-11a. The recombinant plasmid was used to transfect E. coli BL21(DE3) pLysS and sbPTHrP(1-125) synthesis was induced by addition of 1mM isopropyl-beta-d-thiogalactopyranoside. The rapid one step isolation method gave pure sbPTHrP(1-125) as judged by SDS-PAGE and yielded up to 40mg/L of culture medium (3.3mg protein/g of bacteria). The bioactivity of recombinant sbPTHrP(1-125) assessed using an in vitro scale bioassay was found to be equipotent to PTHrP(1-34) in stimulating cAMP accumulation. Assessment of the immunological reactivity of the isolated protein by Western blot revealed it cross-reacts with antisera specific for the N-terminal and C-terminal region of PTHrP. In a radioimmunoassay specific for piscine N-terminal (1-34aa) PTHrP, the recombinant sbPTHrP(1-125) was equipotent with PTHrP(1-34) in displacing labelled (125)I-PTHrP(1-36) PTHrP from the antisera. The availability of recombinant sbPTHrP will allow the development of region specific assays and studies aimed at defining post-secretory processing of this protein and its biological activity in fish.

摘要

报道了利用大肠杆菌系统生产和纯化金头鲷重组甲状旁腺激素相关蛋白[sbPTHrP(1-125)]以及采用连续洗脱凝胶电泳一步纯化法的过程。将编码sbPTHrP(1-125)的cDNA克隆到原核表达载体pET-11a中。用重组质粒转染大肠杆菌BL21(DE3)pLysS,并通过添加1mM异丙基-β-D-硫代半乳糖苷诱导sbPTHrP(1-125)的合成。通过SDS-PAGE判断,这种快速一步分离方法得到了纯的sbPTHrP(1-125),产量高达40mg/L培养基(3.3mg蛋白质/克细菌)。使用体外鳞片生物测定法评估重组sbPTHrP(1-125)的生物活性,发现其在刺激cAMP积累方面与PTHrP(1-34)具有同等效力。通过蛋白质印迹法评估分离蛋白的免疫反应性,发现它与针对PTHrP N端和C端区域的抗血清发生交叉反应。在针对鱼类N端(1-34aa)PTHrP的放射免疫测定中,重组sbPTHrP(1-125)在从抗血清中置换标记的(125)I-PTHrP(1-36) PTHrP方面与PTHrP(1-34)具有同等效力。重组sbPTHrP的可得性将有助于开发区域特异性测定方法,并开展旨在确定该蛋白在鱼类中的分泌后加工及其生物活性的研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验