Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.
Mol Cells. 2020 Sep 30;43(9):804-812. doi: 10.14348/molcells.2020.0163.
In cells, proteins form macromolecular complexes to execute their own unique roles in biological processes. Conventional structural biology methods adopt a bottom-up approach starting from defined sets of proteins to investigate the structures and interactions of protein complexes. However, this approach does not reflect the diverse and complex landscape of endogenous molecular architectures. Here, we introduce a top-down approach called Electron Microscopy screening for endogenous Protein ArchitectureS (EMPAS) to investigate the diverse and complex landscape of endogenous macromolecular architectures in an unbiased manner. By applying EMPAS, we discovered a spiral architecture and identified it as AdhE. Furthermore, we performed screening to examine endogenous molecular architectures of human embryonic stem cells (hESCs), mouse brains, cyanobacteria and plant leaves, revealing their diverse repertoires of molecular architectures. This study suggests that EMPAS may serve as a tool to investigate the molecular architectures of endogenous macromolecular proteins.
在细胞中,蛋白质形成大分子复合物,以在生物过程中执行其独特的功能。传统的结构生物学方法采用自下而上的方法,从定义的蛋白质组开始,研究蛋白质复合物的结构和相互作用。然而,这种方法并不能反映内源性分子结构的多样化和复杂性。在这里,我们引入了一种自上而下的方法,称为电子显微镜筛选内源性蛋白质结构(EMPAS),以无偏倚的方式研究内源性大分子结构的多样化和复杂性。通过应用 EMPAS,我们发现了一种螺旋结构,并将其鉴定为 AdhE。此外,我们进行了筛选,以研究人类胚胎干细胞(hESC)、老鼠大脑、蓝藻和植物叶片中的内源性分子结构,揭示了它们多样化的分子结构谱。这项研究表明,EMPAS 可能成为研究内源性大分子蛋白质分子结构的一种工具。