大肠杆菌裂解物G-CSF结构特征的表征和硅分析

S. Peymanfar, R. Roghanian, K. Ghaedi, Sayed-Hamid Zarkesh-Esfahani, R. Yari
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摘要

目的粒细胞集落刺激因子(G-CSF)具有多种功能,包括刺激造血和粒细胞祖细胞增殖。重组人G-CSF (rh-G-CSF)用于治疗化疗患者的中性粒细胞减少症。成熟的中性粒细胞表达G-CSF受体(G-CSFR),在循环G-CSF清除中具有重要的特异性机制。计算研究是基本的生物信息学方法,用于描述蛋白质的物理化学性质和三维构型,以及重组药物的蛋白质-配体相互作用。我们以前在大肠杆菌中产生了rh-G-CSF,并表明分离的蛋白质在小鼠中具有不可接受的生物活性。在本文中,我们旨在通过分析测试来表征纯化的rh-G-CSF,并通过G-CSF的计算建模建立了体内模型。材料与方法本实验对纯化后的G-CSF进行分析实验。然后,从蛋白质数据库(Protein Data Bank, PDB)中提取晶体结构,并在Amber力场下使用Gromacs 5.1软件包进行分子动力学(MD)模拟。还检测了G-CSF的氨基酸含量对结合相应受体的重要性;此外,还研究了二硫苏糖醇(DTT)在G-CSF纯化中的作用。结果制备的重组G-CSF与标准G-CSF具有相当的特性,且重组G-CSF中氨基酸残留稳定。此外,纯化条件(DTT和多余半胱氨酸的存在)对生成的G-CSF的稳定性和功能有显著影响。结论重组G-CSF的实验分析和计算机分析为其功能和特性提供了良好的信息,可用于工业研究。
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Characterization and In Silico Analysis of The Structural Features of G-CSF Derived from Lysates of Escherichia coli
Objective Granulocyte colony-stimulating factor (G-CSF) has a wide variety of functions including stimulation of hematopoiesis and proliferation of granulocyte progenitor cells. Recombinant human G-CSF (rh-G-CSF) is used for treatment of neutropenia in patients receiving chemotherapy. The mature bloodstream neutrophils express G-CSF receptor (G-CSFR), presenting a significant and specific mechanism for circulating G-CSF clearance. Computational studies are essential bioinformatics methods used for characterization of proteins with regard to their physicochemical properties and 3D configuration, as well as protein–ligand interactions for recombinant drugs. We formerly produced rh-G-CSF in E. coli and showed that the isolated protein had unacceptable biological activity in mice. In the present paper, we aimed to characterize the purified rh-G-CSF by analytical tests and developed an in vivo model by computational modelling of G-CSF. Materials and Methods In this experimental study, we analyzed the purified G-CSF using the analytical experiments. Then, the crystalline structure was extracted from Protein Data Bank (PDB) and molecular dynamics (MD) simulation was performed using Gromacs 5.1 package under an Amber force field. The importance of amino acid contents of G-CSF, to bind the respective receptor was also detected; moreover, the effect of dithiothreitol (DTT) used in G-CSF purification was studied. Results The results revealed that characteristics of the produced recombinant G-CSF were comparable with those of the standard G-CSF and the recombinant G-CSF with the residual amino acid was stable. Also, purification conditions (DTT and existence of extra cysteine) had a significant effect on the stability and functionality of the produced G-CSF. Conclusion Experimental and in silico analyses provided good information regarding the function and characteristics of our recombinant G-CSF which could be useful for industrial researches.
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