Dependence of phase transition uniformity on crystal sizes characterized using birefringence.

IF 2.3 2区 物理与天体物理 Q3 CHEMISTRY, PHYSICAL Structural Dynamics-Us Pub Date : 2021-06-30 eCollection Date: 2021-05-01 DOI:10.1063/4.0000098
Saminathan Ramakrishnan, Jason R Stagno, Valentin Magidson, William F Heinz, Yun-Xing Wang
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引用次数: 1

Abstract

Solid-solid phase transitions (SSPTs) have been widely observed in crystals of organic or inorganic small-molecules. Although SSPTs in macromolecular crystals have been reported, the majority involve local atomic changes, such as those induced by changes in hydration. SSPTs driven by large conformational changes, however, can be more difficult to characterize since they often significantly disrupt lattice packing interactions. Such drastic changes make the cooperativity of molecular motion at the atomic level less easily achieved and more dependent on intrinsic properties of the crystal that define lattice order. Here, we investigate the effect of crystal size on the uniformity of SSPT in thin plate-like crystals of the adenine riboswitch aptamer RNA (riboA) by monitoring changes in crystal birefringence upon the diffusion of adenine ligand. The birefringence intensity is directly related to molecular order and the concurrent changes to polarizability of molecules that results from structural changes throughout the phase transition. The riboA crystals were loosely grouped into three categories (small, medium, and large) based on the surface area of the crystal plates. The time width of transition increased as a function of crystal size, ranging from ∼13 s for small crystals to ∼40 s for the largest crystal. Whereas the transitions in small crystals (<10 μm2) were mostly uniform throughout, the medium and large crystals exhibited large variations in the time and width of the transition peak depending on the region of the crystal being analyzed. Our study provides insight into the spatiotemporal behavior of phase transitions in crystals of biological molecules and is of general interest to time-resolved crystallographic studies, where the kinetics of conformational changes may be governed by the kinetics of an associated SSPT.

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相变均匀性对使用双折射表征的晶体尺寸的依赖性。
在有机或无机小分子的晶体中已经广泛观察到固体-固体相变(SSPTs)。尽管已经报道了大分子晶体中的SSPT,但大多数涉及局部原子变化,例如由水合变化引起的变化。然而,由大构象变化驱动的SSPT可能更难表征,因为它们通常会显著破坏晶格堆积相互作用。这种剧烈的变化使得分子运动在原子水平上的协同性不太容易实现,并且更依赖于定义晶格顺序的晶体的固有性质。在这里,我们通过监测腺嘌呤配体扩散时晶体双折射的变化,研究了晶体尺寸对腺嘌呤核糖开关适体RNA(ribA)薄板状晶体中SSPT均匀性的影响。双折射强度与分子顺序和分子极化率的同时变化直接相关,这些变化是由整个相变过程中的结构变化引起的。根据晶体板的表面积,核糖A晶体大致分为三类(小、中、大)。转变的时间宽度随着晶体尺寸的变化而增加,范围从~13 s适用于~40的小晶体 s代表最大的水晶。尽管小晶体(μm2)中的跃迁在整个过程中基本上是均匀的,但中晶体和大晶体在跃迁峰的时间和宽度上表现出很大的变化,这取决于所分析的晶体的区域。我们的研究深入了解了生物分子晶体中相变的时空行为,并对时间分辨晶体学研究普遍感兴趣,其中构象变化的动力学可能由相关SSPT的动力学控制。
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来源期刊
Structural Dynamics-Us
Structural Dynamics-Us CHEMISTRY, PHYSICALPHYSICS, ATOMIC, MOLECU-PHYSICS, ATOMIC, MOLECULAR & CHEMICAL
CiteScore
5.50
自引率
3.60%
发文量
24
审稿时长
16 weeks
期刊介绍: Structural Dynamics focuses on the recent developments in experimental and theoretical methods and techniques that allow a visualization of the electronic and geometric structural changes in real time of chemical, biological, and condensed-matter systems. The community of scientists and engineers working on structural dynamics in such diverse systems often use similar instrumentation and methods. The journal welcomes articles dealing with fundamental problems of electronic and structural dynamics that are tackled by new methods, such as: Time-resolved X-ray and electron diffraction and scattering, Coherent diffractive imaging, Time-resolved X-ray spectroscopies (absorption, emission, resonant inelastic scattering, etc.), Time-resolved electron energy loss spectroscopy (EELS) and electron microscopy, Time-resolved photoelectron spectroscopies (UPS, XPS, ARPES, etc.), Multidimensional spectroscopies in the infrared, the visible and the ultraviolet, Nonlinear spectroscopies in the VUV, the soft and the hard X-ray domains, Theory and computational methods and algorithms for the analysis and description of structuraldynamics and their associated experimental signals. These new methods are enabled by new instrumentation, such as: X-ray free electron lasers, which provide flux, coherence, and time resolution, New sources of ultrashort electron pulses, New sources of ultrashort vacuum ultraviolet (VUV) to hard X-ray pulses, such as high-harmonic generation (HHG) sources or plasma-based sources, New sources of ultrashort infrared and terahertz (THz) radiation, New detectors for X-rays and electrons, New sample handling and delivery schemes, New computational capabilities.
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