School of Biomedical Sciences, Faculty of Health Sciences, Curtin Health Innovation Research Institute, Curtin University, Bentley, Western Australia, Australia.
School of Psychiatry and Clinical Neurosciences, University of Western Australia, Crawley, Western Australia, Australia.
Sci Rep. 2018 Aug 27;8(1):12834. doi: 10.1038/s41598-018-30788-w.
Baculoviral protein expression in insect cells has been previously used to generate large quantities of a protein of interest for subsequent use in biochemical and structural analyses. The MultiBac baculovirus protein expression system has enabled, the use of a single baculovirus to reconstitute a protein complex of interest, resulting in a larger protein yield. Using this system, we aimed to reconstruct the gamma (γ)-secretase complex, a multiprotein enzyme complex essential for the production of amyloid-β (Aβ) protein. A MultiBac vector containing all components of the γ-secretase complex was generated and expression was observed for all components. The complex was active in processing APP and Notch derived γ-secretase substrates and proteolysis could be inhibited with γ-secretase inhibitors, confirming specificity of the recombinant γ-secretase enzyme. Finally, affinity purification was used to purify an active recombinant γ-secretase complex. In this study we demonstrated that the MultiBac protein expression system can be used to generate an active γ-secretase complex and provides a new tool to study γ-secretase enzyme and its variants.
杆状病毒蛋白在昆虫细胞中的表达以前曾被用于生成大量目的蛋白,以供随后进行生化和结构分析。MultiBac 杆状病毒蛋白表达系统能够使用单个杆状病毒重新构成目的蛋白复合物,从而提高蛋白产量。使用该系统,我们旨在重建 γ-分泌酶复合物,这是一种多蛋白酶复合物,对于淀粉样蛋白-β(Aβ)蛋白的产生至关重要。生成了一个包含 γ-分泌酶复合物所有成分的 MultiBac 载体,并观察到所有成分的表达。该复合物能够有效处理 APP 和 Notch 衍生的 γ-分泌酶底物,并且可以用 γ-分泌酶抑制剂抑制蛋白水解,从而证实了重组 γ-分泌酶酶的特异性。最后,使用亲和纯化法纯化了活性的重组 γ-分泌酶复合物。在这项研究中,我们证明了 MultiBac 蛋白表达系统可用于生成活性 γ-分泌酶复合物,并为研究 γ-分泌酶酶及其变体提供了新工具。