EMPAS: Electron Microscopy Screening for Endogenous Protein Architectures

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 app...

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Published inMolecules and cells Vol. 43; no. 9; pp. 804 - 812
Main Authors Kim, Gijeong, Jang, Seongmin, Lee, Eunhye, Song, Ji-Joon
Format Journal Article
LanguageEnglish
Published United States Korean Society for Molecular and Cellular Biology 30.09.2020
한국분자세포생물학회
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ISSN1016-8478
0219-1032
DOI10.14348/molcells.2020.0163

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Summary: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.
Bibliography:http://www.molcells.org/journal/view.html?doi=10.14348/molcells.2020.0163
ISSN:1016-8478
0219-1032
DOI:10.14348/molcells.2020.0163