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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Site-directed spin labeling and chemical crosslinking demonstrate that helix V is close to helices VII and VIII in the lactose permease of Escherichia coli
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Site-directed spin labeling and chemical crosslinking demonstrate that helix V is close to helices VII and VIII in the lactose permease of Escherichia coli

机译:定点旋转标记和化学交联表明,螺旋V在大肠杆菌的乳糖通透酶中接近于螺旋VII和VIII。

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摘要

Site-directed chemical cleavage of lactose permease indicates that helix V is in close proximity to helices VII and VIII. To test this conclusion further, permease containing a biotin-acceptor domain and paired Cys residues at positions 148 (helix V) and 228 (helix VII), 148 and 226 (helix VII), or 148 and 275 (helix VIII) was affinity purified and labeled with a sulfhydryl-specific nitroxide spin label. Spin-spin interactions are observed with the 148/228 and 148/275 pairs, indicating close proximity between appropri- ate faces of helix V and helices VII and VIII.
机译:乳糖通透酶的定点化学切割表明,螺旋V与螺旋VII和VIII非常接近。为了进一步测试该结论,亲和纯化了含有生物素受体结构域和在位置148(螺旋V)和228(螺旋VII),148和226(螺旋VII)或148和275(螺旋VIII)的成对Cys残基的通透酶并用巯基特异性的一氧化氮自旋标记物标记。在148/228和148/275对中观察到了自旋-自旋相互作用,表明螺旋V和螺旋VII和VIII的适当面之间非常接近。

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