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首页> 外文期刊>Journal of cellular biochemistry. >Structure and growth of ultrasmall protein microcrystals by synchrotron radiation: II. microGISAX and microscopy of lysozyme.
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Structure and growth of ultrasmall protein microcrystals by synchrotron radiation: II. microGISAX and microscopy of lysozyme.

机译:超小蛋白质微晶的结构和生长通过同步加速器辐射:II。 microGISAX和溶菌酶显微镜。

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摘要

The early steps of growth and nucleation of the lysozyme microcrystals by classical and nanotemplate-based hanging vapor diffusion methods are studied using microGISAXS at the European Synchrotron Radiation Facility (ESRF) in Grenoble, France. Out-of-plane cuts in the Yoneda regions of the 2D scattering profiles point to the detection of ultrasmall lysozyme crystals by microGISAXS quite before than by light microscopy. Furthermore lysozyme crystal formation occurs quite earlier with the nanotemplate than with the classical method. Our data are compatible with two distinct modes of crystal nucleation and growth for P450sc and lysozyme.
机译:在法国格勒诺布尔的欧洲同步加速器辐射设施(ESRF)上使用microGISAXS研究了通过经典的和基于纳米模板的悬挂蒸汽扩散方法,溶菌酶微晶的生长和成核的早期步骤。 2D散射曲线的Yoneda区域中的平面外切割表明,与通过光学显微镜检测之前相比,microGISAXS可以检测超小溶菌酶晶体。此外,与传统方法相比,纳米模板的溶菌酶晶体形成要早得多。我们的数据与P450sc和溶菌酶的两种不同的晶体成核和生长模式不同。

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