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10.1016/j.str.2014.09.017

http://scihub22266oqcxt.onion/10.1016/j.str.2014.09.017
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C4255137!4255137!25456413
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suck abstract from ncbi


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pmid25456413      Structure 2014 ; 22 (12): 1875-82
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  • Controlled Bacterial Lysis for Electron Tomography of Native Cell Membranes #MMPMID25456413
  • Fu X; Himes B; Ke D; Rice WJ; Ning J; Zhang P
  • Structure 2014[Dec]; 22 (12): 1875-82 PMID25456413show ga
  • Cryo-electron tomography (cryoET) has become a powerful tool for direct visualization of 3D structures of native biological specimens at molecular resolution, but its application is limited to thin specimens (<300 nm). Recently, vitreous sectioning and cryo-FIB milling technologies were developed to physically reduce the specimen thickness; however, cryoET analysis of membrane protein complexes within native cell membranes remains a great challenge. Here, we use phage ?X174 lysis gene E to rapidly produce native, intact, bacterial cell membranes for high resolution cryoET. We characterized E gene-induced cell lysis using FIB/SEM and cryoEM and show that the bacteria cytoplasm was largely depleted through spot lesion, producing ghosts with the cell membranes intact. We further demonstrate the utility of E-gene-induced lysis for cryoET using the bacterial chemotaxis receptor signaling complex array. The described method should have a broad application for structural and functional studies of native, intact cell membranes and membrane protein complexes.
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