Protein electrostatic potential Fourier maps calculated using the transferable aspherical atom model and the independent atom model across resolutions

IF 3.5 2区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
IUCrJ Pub Date : 2025-11-01 Epub Date: 2025-10-17 DOI:10.1107/S2052252525008383
Marta Kulik , Paulina Maria Dominiak
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引用次数: 0

Abstract

Electrostatic potential maps of proteins are calculated at various resolutions using the transferable aspherical atom model (TAAM) to determine the relations between the electrostatic potential and resolution for different atom types.
Common sense tells us that experimental maps of lower (worse) resolution obtained from cryogenic electron microscopy or three-dimensional electron diffraction convey less information than maps of higher (better) resolution. However, information regarding the presence of charged moieties is more visible at lower resolutions. To investigate this phenomenon from a theoretical perspective, we analyzed the effects of truncation of data from the high-resolution end (from 1 Å to 8 Å) on theoretical Fourier images of the electrostatic potential of protein crystals, using both the popular independent atom model (IAM) of scattering factors and the more accurate transferable aspherical atom model (TAAM) combined with the UBDB/MATTS data bank. We compared our findings with those obtained for theoretical Fourier images of electron density maps associated with X-ray diffraction. Strikingly, when IAM is applied, there is almost no qualitative difference between the Fourier maps of electrostatic potential and electron density, regardless of their resolution. In contrast, the Fourier electrostatic potential maps calculated with TAAM, when of lower resolution, strongly differ from the electron density maps at the positions of charged moieties. Comparing TAAM and IAM, in the case of Fourier electrostatic potential maps, the relative difference between them is usually greatest at lower resolution maps, with a noticeable dependence on atom type and charge. In the case of Fourier electron density maps, this relative difference is much smaller and becomes more apparent in higher resolution maps. Thus, the use of accurate scattering factors is much more important for lower resolution data than for higher resolution data if one wants to investigate charged systems.
利用可转移非球面原子模型和独立原子模型计算蛋白质静电电位傅立叶图。
常识告诉我们,低温电子显微镜或三维电子衍射获得的低(较差)分辨率的实验图比高(较好)分辨率的图传达的信息少。然而,关于带电部分存在的信息在较低的分辨率下更明显。为了从理论角度研究这一现象,我们使用流行的散射因子独立原子模型(IAM)和更精确的可转移非球面原子模型(TAAM)结合UBDB/MATTS数据库,分析了高分辨率端(从1 Å到8 Å)数据截断对蛋白质晶体静电势理论傅里叶图像的影响。我们将我们的发现与x射线衍射相关的电子密度图的理论傅里叶图像进行了比较。引人注目的是,当应用IAM时,无论其分辨率如何,静电势和电子密度的傅里叶图之间几乎没有定性差异。相反,用TAAM计算的傅里叶静电势图,当分辨率较低时,与带电部分位置的电子密度图有很大的不同。比较TAAM和IAM,在傅里叶静电势图的情况下,它们之间的相对差异通常在低分辨率图中最大,并且明显依赖于原子类型和电荷。在傅里叶电子密度图的情况下,这种相对差异要小得多,并且在更高分辨率的图中变得更加明显。因此,如果要研究带电系统,使用精确的散射因子对于低分辨率数据比对于高分辨率数据更为重要。
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
IUCrJ
IUCrJ CHEMISTRY, MULTIDISCIPLINARYCRYSTALLOGRAPH-CRYSTALLOGRAPHY
CiteScore
7.50
自引率
5.10%
发文量
95
审稿时长
10 weeks
期刊介绍: IUCrJ is a new fully open-access peer-reviewed journal from the International Union of Crystallography (IUCr). The journal will publish high-profile articles on all aspects of the sciences and technologies supported by the IUCr via its commissions, including emerging fields where structural results underpin the science reported in the article. Our aim is to make IUCrJ the natural home for high-quality structural science results. Chemists, biologists, physicists and material scientists will be actively encouraged to report their structural studies in IUCrJ.
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