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蛋白质从脂质层生长晶体的机制。

The mechanism of protein crystal growth from lipid layers.

作者信息

Hemming S A, Bochkarev A, Darst S A, Kornberg R D, Ala P, Yang D S, Edwards A M

机构信息

Department of Pathology, McMaster University, Hamilton, Ontario, Canada.

出版信息

J Mol Biol. 1995 Feb 17;246(2):308-16. doi: 10.1006/jmbi.1994.0086.

Abstract

Two-dimensional (2D) crystals of proteins on lipid monolayers can initiate the formation of large three-dimensional (3D) crystals suitable for X-ray diffraction studies. The role of the 2D crystals in this process has not been firmly established. While it is likely that the 2D crystals serve as nuclei for epitaxial crystal growth, other mechanisms, such as non-specific nucleation induced by the high local concentration of the protein at the surface of the lipid layer, cannot be excluded. Using streptavidin as a model system, we have now firmly established that 3D crystal growth from 2D crystals on lipid layers occurs by epitaxy. We show that 2D crystals of streptavidin (space group C222) on biotinated lipid layers nucleate the growth of a 3D crystal form (space group I4I22) that possesses a structural similarity with the 2D crystal, but have no effect on the growth of 3D crystal forms (I222 and P2(1)) that are unrelated to the 2D crystal. At lower pH, a new 3D crystal form (space group P1), unrelated to the previously described 2D crystals, grew from lipid layers. This discovery initially raised concern about the validity of the epitaxial mechanism, but these concerns were alleviated with the subsequent discovery of a structurally related 2D P1 crystal that grew in similar solution conditions. Some parameters affecting epitaxial growth of both the P1 and I4I22 crystals were investigated, revealing several noteworthy features of the epitaxial growth. (1) 2D crystals are very effective nucleating agents; for instance, the P1 2D crystals can direct the growth of P1 3D crystals even under conditions that favour the growth of other crystal forms. (2) The epitaxial 3D crystal grow very rapidly and at amazingly low protein concentrations; P1 3D crystals can be grown from solutions as low as 10 microM streptavidin. (3) There is no obligate requirement for the deposition of pre-formed 2D crystals; lipid layers alone are equally effective at promoting epitaxial crystal growth.

摘要

脂质单分子层上蛋白质的二维(2D)晶体可引发适合X射线衍射研究的大型三维(3D)晶体的形成。二维晶体在此过程中的作用尚未完全明确。虽然二维晶体可能作为外延晶体生长的晶核,但其他机制,如脂质层表面蛋白质高局部浓度诱导的非特异性成核,也不能排除。以链霉亲和素作为模型系统,我们现已确定脂质层上二维晶体的三维晶体生长是通过外延发生的。我们表明,生物素化脂质层上链霉亲和素的二维晶体(空间群C222)可使一种三维晶体形式(空间群I4I22)的生长成核,该三维晶体形式与二维晶体具有结构相似性,但对与二维晶体无关的三维晶体形式(I222和P2(1))的生长没有影响。在较低pH值下,一种与先前描述的二维晶体无关的新三维晶体形式(空间群P1)从脂质层生长出来。这一发现最初引发了对外延机制有效性的担忧,但随后发现了在相似溶液条件下生长的结构相关的二维P1晶体,这些担忧便得到了缓解。研究了影响P1和I4I22晶体外延生长的一些参数,揭示了外延生长的几个值得注意的特征。(1)二维晶体是非常有效的成核剂;例如,即使在有利于其他晶体形式生长的条件下,P1二维晶体也能引导P1三维晶体的生长。(2)外延三维晶体生长非常迅速,且在极低的蛋白质浓度下即可发生;P1三维晶体可从低至10微摩尔链霉亲和素的溶液中生长出来。(3)并非必须沉积预先形成的二维晶体;仅脂质层在促进外延晶体生长方面同样有效。

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