Shelby M L, Gilbile D, Grant T D, Bauer W J, Segelke B, He W, Evans A C, Crespo N, Fischer P, Pakendorf T, Hennicke V, Hunter M S, Batyuk A, Barthelmess M, Meents A, Kuhl T L, Frank M, Coleman M A
Biosciences and Biotechnology Division, Lawrence Livermore National Laboratory, Livermore, CA, USA.
Department of Chemical Engineering, University of California at Davis, Davis, CA, USA.
Crystals (Basel). 2020 Oct;10(10). doi: 10.3390/cryst10100886. Epub 2020 Oct 1.
Nanolipoprotein particles (NLPs), also called "nanodiscs", are discoidal particles with a patch of lipid bilayer corralled by apolipoproteins. NLPs have long been of interest due to both their utility as membrane-model systems into which membrane proteins can be inserted and solubilized and their physiological role in lipid and cholesterol transport via HDL and LDL maturation, which are important for human health. Serial femtosecond crystallography (SFX) at X-ray free electron lasers (XFELs) is a powerful approach for structural biology of membrane proteins, which are traditionally difficult to crystallize as large single crystals capable of producing high-quality diffraction suitable for structure determination. To facilitate understanding of the specific role of two apolipoprotein/lipid complexes, ApoA1 and ApoE4, in lipid binding and HDL/LDL particle maturation dynamics and develop new SFX methods involving NLP membrane protein encapsulation, we have prepared and crystallized homogeneous populations of ApoA1 and ApoE4 NLPs. Crystallization of empty NLPs yields semi-ordered objects that appear crystalline and give highly anisotropic and diffuse X-ray diffraction, similar in characteristics to fiber diffraction. Several unit cell parameters were approximately determined for both NLPs from these measurements. Thus, low-background, sample conservative methods of delivery are critical. Here we implemented a fixed target sample delivery scheme utilizing the Roadrunner fast-scanning system and ultra-thin polymer/graphene support films, providing a low-volume, low-background approach to membrane protein SFX. This study represents initial steps in obtaining structural information for ApoA1 and ApoE4 NLPs and developing this system as a supporting scaffold for future structural studies of membrane proteins crystalized in a native lipid environment.
纳米脂蛋白颗粒(NLPs),也被称为“纳米盘”,是一种盘状颗粒,其脂质双层斑块由载脂蛋白围成。由于NLPs既可用作膜模型系统,可将膜蛋白插入其中并使其溶解,又在通过高密度脂蛋白(HDL)和低密度脂蛋白(LDL)成熟进行脂质和胆固醇运输中发挥生理作用,而这对人类健康至关重要,因此长期以来一直备受关注。在X射线自由电子激光(XFELs)上进行的串行飞秒晶体学(SFX)是研究膜蛋白结构生物学的一种强大方法,传统上,膜蛋白很难结晶成能够产生适合结构测定的高质量衍射的大单晶。为了便于理解两种载脂蛋白/脂质复合物ApoA1和ApoE4在脂质结合以及HDL/LDL颗粒成熟动力学中的具体作用,并开发涉及NLP膜蛋白封装的新SFX方法,我们制备了ApoA1和ApoE4 NLPs的均匀群体并使其结晶。空NLPs的结晶产生了半有序物体,这些物体看起来呈晶体状,并给出高度各向异性和漫射的X射线衍射,其特征与纤维衍射相似。通过这些测量,大致确定了两种NLPs的几个晶胞参数。因此,低背景、样品保守的递送方法至关重要。在这里,我们利用Roadrunner快速扫描系统和超薄聚合物/石墨烯支撑膜实施了一种固定靶样品递送方案,为膜蛋白SFX提供了一种低体积、低背景的方法。这项研究代表了获取ApoA1和ApoE4 NLPs结构信息以及将该系统开发为在天然脂质环境中结晶的膜蛋白未来结构研究的支撑支架的初步步骤。