在中分辨率低温电子密度图中识别氨基酸侧链。

IF 5.2 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2025-08-01 DOI:10.1002/pro.70217
Dibyendu Mondal, Vipul Kumar, Tadej Satler, Rakesh Ramachandran, Daniel Saltzberg, Ilan Chemmama, Kala Bharath Pilla, Ignacia Echeverria, Benjamin M Webb, Meghna Gupta, Klim Verba, Andrej Sali
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引用次数: 0

摘要

在低于3 Å分辨率的低温电子显微镜(cryo-EM)图中建立蛋白质的精确原子结构模型是困难的。为了方便这项任务,我们设计了一种方法,将氨基酸残基序列分配到输入低温电镜图(EMSequenceFinder)中追踪的主链片段。EMSequenceFinder依靠贝叶斯评分功能,根据密度图、图分辨率和二级结构倾向对给定主链位置上的20种标准氨基酸残基类型进行排序。通过卷积神经网络对从3-10 Å分辨率的冷冻电镜图中提取的约556万个氨基酸残基密度和沉积在电子显微镜数据库(EMDB)中的相应原子结构模型进行训练,对密度的拟合进行量化。我们对EMSequenceFinder进行了基准测试,通过预测58,044个不同的j -螺旋和β-链片段的序列,给出了片段主链坐标在它们的密度图中拟合。在77.8%的情况下,EMSequenceFinder将正确的序列识别为得分最高的序列。我们还评估了EMSequenceFinder在4到6分辨率的低温电镜图上的独立数据集Å。EMSequenceFinder的准确率(58%)优于经过测试的三种最先进的方法,包括findMysequence(45%)、ModelAngelo(27%)和Phenix中的sequence_from_map(12.9%)。我们进一步通过将严重急性呼吸综合征冠状病毒2非结构蛋白2序列插入到8个分辨率从3.7到7.0 Å的冷冻电镜图中来说明EMSequenceFinder。EMSequenceFinder是在我们的开源集成建模平台(IMP)程序中实现的。因此,基于低温电镜图谱和其他信息,如蛋白质复合物组分的模型和它们之间的化学交联,有望有助于构建整体结构模型。EMSequenceFinder是我们开源IMP发行版的一部分,网址是https://integrativemodeling.org/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recognizing amino acid sidechains in a medium-resolution cryo-electron density map.

Building an accurate atomic structure model of a protein into a cryo-electron microscopy (cryo-EM) map at worse than 3 Å resolution is difficult. To facilitate this task, we devised a method for assigning the amino acid residue sequence to the backbone fragments traced in an input cryo-EM map (EMSequenceFinder). EMSequenceFinder relies on a Bayesian scoring function for ranking 20 standard amino acid residue types at a given backbone position, based on the fit to a density map, map resolution, and secondary structure propensity. The fit to a density is quantified by a convolutional neural network that was trained on ~5.56 million amino acid residue densities extracted from cryo-EM maps at 3-10 Å resolution and corresponding atomic structure models deposited in the Electron Microscopy Data Bank (EMDB). We benchmarked EMSequenceFinder by predicting the sequences of 58,044 distinct ɑ-helix and β-strand fragments, given the fragment backbone coordinates fitted in their density maps. EMSequenceFinder identifies the correct sequence as the best-scoring sequence in 77.8% of these cases. We also assessed EMSequenceFinder on separate datasets of cryo-EM maps at resolutions from 4 to 6 Å. The accuracy of EMSequenceFinder (58%) was better than that of three tested state-of-the-art methods, including findMysequence (45%), ModelAngelo (27%), and sequence_from_map in Phenix (12.9%). We further illustrate EMSequenceFinder by threading the Severe Acute Respiratory Syndrome Coronavirus 2 Non-Structural Protein 2 sequence into eight cryo-EM maps at resolutions from 3.7 to 7.0 Å. EMSequenceFinder is implemented in our open-source Integrative Modeling Platform (IMP) program. Thus, it is expected to be helpful for integrative structure modeling based on a cryo-EM map and other information, such as models of protein complex components and chemical crosslinks between them. EMSequenceFinder is available as part of our open-source IMP distribution at https://integrativemodeling.org/.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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