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利用聚苯乙烯珠去除去污剂,形成大肠杆菌葡萄糖醛酸转移酶的二维晶体阵列。

Two-dimensional crystalline array formation of glucuronide transporter from Escherichia coli by the use of polystyrene beads for detergent removal.

机构信息

Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba Central-6 1-1-1 Higashi, Tsukuba, Ibaraki 305-8566, Japan.

出版信息

J Membr Biol. 2013 Mar;246(3):199-207. doi: 10.1007/s00232-012-9521-8. Epub 2012 Nov 28.

Abstract

n-Dodecyl-β-D-maltoside solubilized glucuronide transporter (GusB), the product of gusB gene from Escherichia coli, was treated with Bio-Beads as an agent for removing the detergent from a micellar solution under suitable combination with dimyristoylphosphatidylcholine. Optimizing conditions led to a two-dimensional crystalline array formation of GusB. The crystalline arrays appear to have a hexagonal lattice with layer group P6, the unit cell dimensions of a = b = 13.8 nm and γ = 120°. Each stain-protruding periodic unit showed approximately 11.8 ± 0.3 nm in a diameter in the inverse Fourier-filtered image to have formed with pentameric GusB (5 × 49.7 kDa).

摘要

用生物珠(Bio-Beads)作为去污剂处理 n-十二烷基-β-D-麦芽糖苷增溶的葡萄糖醛酸转移酶(GusB),该酶来自大肠杆菌的 gusB 基因,与二肉豆蔻酰基磷脂酰胆碱(dimyristoylphosphatidylcholine)适当地组合,以从胶束溶液中除去去污剂。优化条件导致 GusB 的二维结晶阵列形成。结晶阵列似乎具有层群 P6 的六方晶格,晶胞参数 a = b = 13.8nm 和 γ = 120°。每个染色突出的周期性单位在傅里叶逆滤波图像中显示约 11.8 ± 0.3nm 的直径,以五聚体 GusB(5×49.7kDa)的形式形成。

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