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探索密码子优化和响应面法以在大肠杆菌中表达具有生物活性的跨膜RANKL。

Exploring codon optimization and response surface methodology to express biologically active transmembrane RANKL in E. coli.

作者信息

Maharjan Sushila, Singh Bijay, Bok Jin-Duck, Kim Jeong-In, Jiang Tao, Cho Chong-Su, Kang Sang-Kee, Choi Yun-Jaie

机构信息

Department of Agricultural Biotechnology, Seoul National University, Seoul, Republic of Korea; Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea.

Research Institute of Eco-friendly Animal Science, Institute of Green-Bio Science and Technology, Seoul National University, Kangwon-Do, Republic of Korea.

出版信息

PLoS One. 2014 May 8;9(5):e96259. doi: 10.1371/journal.pone.0096259. eCollection 2014.

Abstract

Receptor activator of nuclear factor (NF)-κB ligand (RANKL), a master cytokine that drives osteoclast differentiation, activation and survival, exists in both transmembrane and extracellular forms. To date, studies on physiological role of RANKL have been mainly carried out with extracellular RANKL probably due to difficulties in achieving high level expression of functional transmembrane RANKL (mRANKL). In the present study, we took advantage of codon optimization and response surface methodology to optimize the soluble expression of mRANKL in E. coli. We optimized the codon usage of mRANKL sequence to a preferred set of codons for E. coli changing its codon adaptation index from 0.64 to 0.76, tending to increase its expression level in E. coli. Further, we utilized central composite design to predict the optimum combination of variables (cell density before induction, lactose concentration, post-induction temperature and post-induction time) for the expression of mRANKL. Finally, we investigated the effects of various experimental parameters using response surface methodology. The best combination of response variables was 0.6 OD600, 7.5 mM lactose, 26°C post-induction temperature and 5 h post-induction time that produced 52.4 mg/L of fusion mRANKL. Prior to functional analysis of the protein, we purified mRANKL to homogeneity and confirmed the existence of trimeric form of mRANKL by native gel electrophoresis and gel filtration chromatography. Further, the biological activity of mRANKL to induce osteoclast formation on RAW264.7 cells was confirmed by tartrate resistant acid phosphatase assay and quantitative real-time polymerase chain reaction assays. Importantly, a new finding from this study was that the biological activity of mRANKL is higher than its extracellular counterpart. To the best of our knowledge, this is the first time to report heterologous expression of mRANKL in soluble form and to perform a comparative study of functional properties of both forms of RANKL.

摘要

核因子(NF)-κB 受体激活剂配体(RANKL)是驱动破骨细胞分化、激活和存活的主要细胞因子,以跨膜和细胞外两种形式存在。迄今为止,由于难以实现功能性跨膜RANKL(mRANKL)的高水平表达,关于RANKL生理作用的研究主要是针对细胞外RANKL进行的。在本研究中,我们利用密码子优化和响应面法优化了mRANKL在大肠杆菌中的可溶性表达。我们将mRANKL序列的密码子使用情况优化为大肠杆菌偏好的一组密码子,使其密码子适应指数从0.64提高到0.76,这倾向于提高其在大肠杆菌中的表达水平。此外,我们利用中心复合设计预测mRANKL表达的变量(诱导前细胞密度、乳糖浓度、诱导后温度和诱导后时间)的最佳组合。最后,我们使用响应面法研究了各种实验参数的影响。响应变量的最佳组合是0.6 OD600、7.5 mM乳糖、26°C诱导后温度和5小时诱导后时间,产生了52.4 mg/L的融合mRANKL。在对该蛋白进行功能分析之前,我们将mRANKL纯化至同质,并通过非变性凝胶电泳和凝胶过滤色谱法确认了mRANKL三聚体形式的存在。此外,通过抗酒石酸酸性磷酸酶测定和定量实时聚合酶链反应测定,证实了mRANKL在RAW264.7细胞上诱导破骨细胞形成的生物活性。重要的是,本研究的一个新发现是mRANKL的生物活性高于其细胞外对应物。据我们所知,这是首次报道以可溶性形式异源表达mRANKL并对两种形式的RANKL的功能特性进行比较研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9f6/4014495/1565c4655c0d/pone.0096259.g001.jpg

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