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- W2891210166 endingPage "70" @default.
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- W2891210166 abstract "The need for bacteria to interact with their environment has driven the evolution of elaborate secretion systems. By virtue of their function, secretion systems are macromolecular complexes associated with the cell envelope and therefore inherently difficult to study by conventional structural biology techniques. Cryo-electron microscopy (cryoEM) has become an invaluable technique to study large membrane-embedded complexes and led to major advances in the mechanistic understanding of secretion systems. CryoEM comprises of two main modalities, namely single particle analysis and tomography. Here, we review how detailed structures retrieved by single particle analysis combine elegantly with tomography experiments in which the secretion systems are observed in their native cellular context." @default.
- W2891210166 created "2018-09-27" @default.
- W2891210166 creator A5004830667 @default.
- W2891210166 creator A5010605456 @default.
- W2891210166 creator A5073147933 @default.
- W2891210166 creator A5087426368 @default.
- W2891210166 date "2018-10-01" @default.
- W2891210166 modified "2023-10-17" @default.
- W2891210166 title "CryoEM of bacterial secretion systems" @default.
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- W2891210166 doi "https://doi.org/10.1016/j.sbi.2018.08.007" @default.
- W2891210166 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30223223" @default.
- W2891210166 hasPublicationYear "2018" @default.
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