首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Production of monoclonal antibodies against Chinemys reevesii turtle vitellogenin and their usage for comparison of biochemical and immunological characters of vitellogenins and yolk proteins of freshwater turtles
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Production of monoclonal antibodies against Chinemys reevesii turtle vitellogenin and their usage for comparison of biochemical and immunological characters of vitellogenins and yolk proteins of freshwater turtles

机译:抗里氏中华绒螯蟹卵黄原蛋白原单克隆抗体的制备及其在淡水龟卵黄原蛋白原和卵黄蛋白生化和免疫学特性比较中的应用

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Four hybridoma clones (ACV-1,-3,-4,and -5) were established for Chinemys reevesii (Reeves' turtle) vitellogenin (VTG) as a precursor protein of egg yolk and a biomarker of environmental pollution.Binding-inhibition experiments indicated that the epitopes of four mAbs were distinct.No binding of ACV-4 to C.reevesii VTG in the Western blot suggests that the epitope of ACV-4 would be dependent on the three-dimensional structure.ACV-1,-3,and -5 bound to C.reevesii VTG in the Western blot.The signal for ACV-1 and -5 disappeared by reduction of the VTG,suggesting that the construction of the epitopes for ACV-1 and -5 were dependent on the disulfide bridge in the VTG molecule.All four mAbs recognized Trachemys scripta and Mauremys japonica VTGs in the ELISA.The yolk proteins were tested for the binding of the mAbs in the Western blot.ACV-1 being capable to bind to the VTG in the reduced condition did not bind to any protein bands of the yolk.This indicates that ACV-1 recognizes a part of the VTG molecule that is not incorporated in the oocytes.Both ACV-3 and -5 bound to the 32- and 70-kDa yolk proteins.Since a mAb recognizes only one site (epitope) on a protein molecule,the 32-kDa protein originated from the 70-kDa one.An ELISA system using ACV-5 as the capture antibody and ACV-3 as the detecting antibody showed the lower detectable concentration (2 ng/mL) and a wide detectable range to 1000 ng/mL (R~2=0.999).The system was used to determine serum VTG levels of juvenile turtles treated with estradiol-17beta or vehicle (corn oil).By the use of the mAbs described in this paper,basic and applied studies for turtle VTGs would be improved.
机译:建立了四个杂交瘤细胞克隆(ACV-1,-3,-4和-5),用于里氏中华绒螯蟹卵黄蛋白原蛋白(VTG)作为蛋黄的前体蛋白和环境污染的生物标志物。表示四个mAb的表位是不同的.Western印迹中ACV-4与C.reevesii VTG的结合不表明ACV-4的表位将取决于三维结构.ACV-1,-3, Western印迹中,-5与-5结合到C.reevesiiVTG。ACV-1和-5的信号通过VTG的减少而消失,这表明ACV-1和-5的表位的构建取决于二硫键在ELISA中,所有四个mAb都识别了Trachemys scripta和Mauremys japonica VTG。在蛋白印迹法中测试了蛋黄蛋白与mAb的结合.ACV-1在还原条件下能够与VTG结合不与蛋黄的任何蛋白条带结合。这表明ACV-1识别蛋黄的一部分未整合到卵母细胞中的VTG分子.ACV-3和-5都结合到32-kDa和70-kDa卵黄蛋白上。由于mAb仅识别蛋白质分子上的一个位点(表位),因此32-kDa蛋白起源于来自70kDa的ELISA系统,使用ACV-5作为捕获抗体和ACV-3作为检测抗体,可检测到的浓度较低(2 ng / mL),检测范围宽至1000 ng / mL(R〜 2 = 0.999)。该系统用于确定用雌二醇17β或媒介物(玉米油)处理的幼龟的血清VTG水平。通过使用本文所述的mAb,将改善对乌龟VTG的基础和应用研究。

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