Department of Biotechnology, Institute for Biochemistry, Biotechnology and Bioinformatics, Technische Universität Braunschweig, Spielmannstr. 7, 38106 Braunschweig, Germany; Division of Cellular and Molecular Neurobiology, Zoological Institute, Technische Universität Braunschweig, Spielmannstr. 7, 38106 Braunschweig, Germany.
Division of Cellular and Molecular Neurobiology, Zoological Institute, Technische Universität Braunschweig, Spielmannstr. 7, 38106 Braunschweig, Germany.
N Biotechnol. 2018 Oct 25;45:98-112. doi: 10.1016/j.nbt.2017.12.008. Epub 2017 Dec 28.
Cadherin-2 plays a fundamental role during zebrafish CNS and heart morphogenesis. Profiling zCdh2 expression via antibody staining is essential to achieving better understanding of its role during zebrafish development. Generation of recombinant human antibodies to zCdh2 by phage display was used to identify monoclonal antibodies with reduced unspecific binding patterns when compared to available commercial antibodies. Specificity was profiled using flow cytometry of wild type, zCdh2-defective mutant and zCdh2-GFP zebrafish cells. The epitopes recognized by the novel antibodies were mapped to peptides located in the first or second extracellular domains of zCdh2. These antibodies allowed improved observations of the spatial distribution of zCdh2 from imaging of whole mount zebrafish preparations. Since the generated antibodies are sequence defined, they can always be reconstituted from the information stored in the respective computer file, securing future reproducibility of respective experiments. The results further suggest that sequence defined antibodies with specificities thoroughly controlled by flow cytometry and genetic antigen-defective mutants or knockouts can substantially reduce the risk of misleading, false-positive results in whole mount imaging and other assays, and thus can improve the scientific value of such assays.
钙黏蛋白-2 在斑马鱼中枢神经系统和心脏形态发生中起着至关重要的作用。通过抗体染色对 zCdh2 进行表达谱分析,对于更好地理解其在斑马鱼发育过程中的作用至关重要。通过噬菌体展示生成针对 zCdh2 的重组人抗体,用于鉴定与现有商业抗体相比具有减少非特异性结合模式的单克隆抗体。使用流式细胞术分析野生型、zCdh2 缺陷突变体和 zCdh2-GFP 斑马鱼细胞,对特异性进行分析。通过新型抗体识别的表位被映射到位于 zCdh2 的第一或第二细胞外结构域的肽上。这些抗体允许通过对整个斑马鱼标本进行成像来改善 zCdh2 的空间分布观察。由于生成的抗体是序列定义的,因此可以随时从各自计算机文件中存储的信息重新构建,从而确保未来各自实验的可重复性。结果进一步表明,通过流式细胞术和遗传抗原缺陷突变体或敲除体进行特异性全面控制的序列定义抗体,可以大大降低全标本成像和其他检测中误导性、假阳性结果的风险,从而提高这些检测的科学价值。