Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba Central-6 1-1-1 Higashi, Tsukuba, Ibaraki 305-8566, Japan.
J Membr Biol. 2013 Mar;246(3):199-207. doi: 10.1007/s00232-012-9521-8. Epub 2012 Nov 28.
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).
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。