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脂质立方相中的重原子衍生物:关于鸡卵清溶菌酶与钆-1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸配合物四方衍生物晶体的研究结果。

Heavy-atom derivatives in lipidic cubic phases: results on hen egg-white lysozyme tetragonal derivative crystals with Gd-HPDO3A complex.

作者信息

Girard Eric, Pebay-Peyroula Eva, Vicat Jean, Kahn Richard

机构信息

Institut de Biologie Structurale J.-P. Ebel CEA-CNRS-UJF, UMR 5075, 41 Rue Jules Horowitz, 38027 Grenoble CEDEX 1, France.

出版信息

Acta Crystallogr D Biol Crystallogr. 2004 Aug;60(Pt 8):1506-8. doi: 10.1107/S0907444904011710. Epub 2004 Jul 21.

Abstract

Gd-HPDO3A, a neutral gadolinium complex, is a good candidate for obtaining heavy-atom-derivative crystals by the lipidic cubic phase crystallization method known to be effective for membrane proteins. Gadolinium-derivative crystals of hen egg-white lysozyme were obtained by co-crystallizing the protein with 100 mM Gd-HPDO3A in a monoolein cubic phase. Diffraction data were collected to a resolution of 1.7 A using Cu Kalpha radiation from a rotating-anode generator. Two binding sites of the gadolinium complex were located from the strong gadolinium anomalous signal. The Gd-atom positions and their refined occupancies were found to be identical to those found in derivative crystals of hen egg-white lysozyme obtained by co-crystallizing the protein with 100 mM Gd-HPDO3A using the hanging-drop technique. Moreover, the refined structures are isomorphous. The lipidic cubic phase is not disturbed by the high concentration of Gd-HPDO3A. This experiment demonstrates that a gadolinium complex, Gd-HPDO3A, can be used to obtain derivative crystals by the lipidic cubic phase crystallization method. Further studies with membrane proteins that are known to crystallize in lipidic cubic phases will be undertaken with Gd-HPDO3A and other Gd complexes to test whether derivative crystals with high Gd-site occupancies can be obtained.

摘要

钆-六氢吡啶二氧代戊二酸(Gd-HPDO3A)是一种中性钆配合物,是通过脂质立方相结晶法获得重原子衍生物晶体的良好候选物,该方法对膜蛋白有效。通过在单油酸甘油酯立方相中使蛋白质与100 mM Gd-HPDO3A共结晶,获得了鸡蛋清溶菌酶的钆衍生物晶体。使用旋转阳极发生器产生的Cu Kα辐射收集衍射数据,分辨率达到1.7 Å。从强烈的钆反常信号中确定了钆配合物的两个结合位点。发现钆原子的位置及其精修占有率与通过悬滴法使蛋白质与100 mM Gd-HPDO3A共结晶获得的鸡蛋清溶菌酶衍生物晶体中的相同。此外,精修后的结构是同晶型的。脂质立方相不受高浓度Gd-HPDO3A的干扰。该实验表明,钆配合物Gd-HPDO3A可用于通过脂质立方相结晶法获得衍生物晶体。将使用Gd-HPDO3A和其他钆配合物对已知在脂质立方相中结晶的膜蛋白进行进一步研究,以测试是否可以获得具有高钆位点占有率的衍生物晶体。

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