Non-invasive nanoscale imaging of protein micro- and nanocrystals for screening crystallization conditions.

IF 6.1 3区 材料科学 Q1 Biochemistry, Genetics and Molecular Biology
Journal of Applied Crystallography Pub Date : 2024-11-22 eCollection Date: 2024-12-01 DOI:10.1107/S1600576724010124
Krishna Prasad Khakurel, Kei Hosomi, Wataru Inami, Kawata Yoshimasa
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引用次数: 0

Abstract

Crystallography has been the routine technique for studying high-resolution structures of proteins for over five decades. A major bottleneck in structure determination of macromolecules is obtaining crystals of a size and quality suitable for single-crystal X-ray crystallography experiments. Many challenging proteins either fail to grow into crystals or fail to grow into crystals of a size suitable for obtaining high-resolution structures using conventional X-ray crystallography. When it comes to smaller crystals, they can be used either for seeding to get larger crystals or for serial crystallography and electron diffraction for obtaining the structures. For both purposes, a limiting step is to non-invasively image such small crystals of sub-micrometre dimensions and to screen the conditions where such crystals prevail. Here we use cathodoluminescence-based (CL-based) nanoscopy to image protein nanocrystals. We show that crystals of micrometre and submicrometre dimensions can be non-invasively imaged by the CL-based nanoscope. The results presented here demonstrate the feasibility of non-invasive imaging of protein crystals with sub-100 nm resolution.

用于筛选结晶条件的蛋白质微晶体和纳米晶体的非侵入性纳米成像。
50多年来,晶体学一直是研究高分辨率蛋白质结构的常规技术。确定大分子结构的主要瓶颈是获得适合单晶x射线晶体学实验的尺寸和质量的晶体。许多具有挑战性的蛋白质要么不能长成晶体,要么不能长成适合使用常规x射线晶体学获得高分辨率结构的尺寸的晶体。当涉及到较小的晶体时,它们既可以用于播种以获得更大的晶体,也可以用于连续晶体学和电子衍射以获得结构。对于这两个目的,一个限制步骤是对这种亚微米尺寸的小晶体进行非侵入性成像,并筛选这种晶体普遍存在的条件。在这里,我们使用基于阴极发光(CL-based)的纳米显微镜来成像蛋白质纳米晶体。我们发现微米和亚微米尺寸的晶体可以通过基于cl的纳米显微镜进行非侵入性成像。本文的结果证明了在100 nm以下分辨率下对蛋白质晶体进行无创成像的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.00
自引率
3.30%
发文量
178
审稿时长
4.7 months
期刊介绍: Many research topics in condensed matter research, materials science and the life sciences make use of crystallographic methods to study crystalline and non-crystalline matter with neutrons, X-rays and electrons. Articles published in the Journal of Applied Crystallography focus on these methods and their use in identifying structural and diffusion-controlled phase transformations, structure-property relationships, structural changes of defects, interfaces and surfaces, etc. Developments of instrumentation and crystallographic apparatus, theory and interpretation, numerical analysis and other related subjects are also covered. The journal is the primary place where crystallographic computer program information is published.
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