Molecular Bioenergetics, Medical School, Goethe-University Frankfurt, Frankfurt am Main, Germany.
Proteomics. 2010 Sep;10(18):3379-87. doi: 10.1002/pmic.201000343.
Here, we expand the application of blue native electrophoresis to the separation of mega protein complexes larger than 10 MDa by introducing novel large pore acrylamide gels. We tailored the bis-acrylamide cross-linker amounts relative to the acrylamide monomer to enlarge the pore size of acrylamide gels and to obtain elastic and sufficiently stable gels. The novel gel types were then used to search for suprastructures of mitochondrial respiratory supercomplexes, the hypothetical respiratory strings, or patches. We identified 4-8 MDa assemblies that contain respiratory complexes I, III, and IV and most likely represent dimers, trimers, and tetramers of respiratory supercomplexes. We also isolated multimeric respiratory supercomplexes with apparent masses of 35-45 MDa, the presumed core pieces of respiratory strings or patches. Electron microscopic investigations will be required to clarify whether the isolated assemblies of complexes are ordered and specific, as predicted for respiratory strings and patches in the mitochondrial membrane.
在这里,我们通过引入新型大孔径丙烯酰胺凝胶,将蓝色 native 电泳的应用扩展到分离大于 10 MDa 的巨型蛋白质复合物。我们相对丙烯酰胺单体调整双丙烯酰胺交联剂的用量,以增大丙烯酰胺凝胶的孔径,并获得有弹性且足够稳定的凝胶。然后,我们使用新型凝胶类型来寻找线粒体呼吸超级复合物的超结构、假设的呼吸串或斑块。我们鉴定出含有呼吸复合物 I、III 和 IV 的 4-8 MDa 组装体,这些组装体很可能代表呼吸超级复合物的二聚体、三聚体和四聚体。我们还分离出具有 35-45 MDa 表观质量的多聚体呼吸超级复合物,这些复合物可能是呼吸串或斑块在线粒体膜中的核心部分。需要进行电子显微镜研究来澄清所分离的复合物组装体是否如线粒体膜中呼吸串或斑块所预测的那样有序和特异。