• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用分子动力学模拟和MM/PBSA预测氨酰-tRNA合成酶对非标准氨基酸的多特异性

Predicting the polyspecificity of aminoacyl-tRNA synthetase for non-canonical amino acids using molecular dynamics simulation and MM/PBSA.

作者信息

Lee Dongheon, Choi Jong-Il

机构信息

Department of Biotechnology and Bioengineering, Chonnam National University, Gwangju, Republic of Korea.

出版信息

PLoS One. 2025 Jan 10;20(1):e0316907. doi: 10.1371/journal.pone.0316907. eCollection 2025.

DOI:10.1371/journal.pone.0316907
PMID:39792834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11723616/
Abstract

With the advancement of genetic code expansion, the field is progressing towards incorporating multiple non-canonical amino acids (ncAAs). The specificity of aminoacyl-tRNA synthetases (aaRSs) towards ncAAs is a critical factor, as engineered aaRSs frequently show polyspecificity, complicating the precise incorporation of multiple ncAAs. To address this challenge, predicting binding affinity can be beneficial. In this study, we expressed sfGFP using an orthogonal aaRS/tRNA pair with 4-Azido-L-phenylalanine (AzF) and another four different ncAAs. The experimental results showed specificity with O-Methyl-L-tyrosine as well as AzF, and these results were compared with computational predictions. We constructed a mutant aaRS structure specific for AzF through homology modelling and conducted docking studies with tyrosine and five ncAAs, followed by molecular dynamics simulations. The binding affinity was calculated using the molecular mechanics/Poisson-Boltzmann surface area, focusing on nonpolar solvation terms. While the analysis is based on the incorporation of limited number of ncAAs, the cavity and dispersion term method showed consistency with experimental data, highlighting its potential utility compared to the surface area term method. These findings enhance understanding of the ncAA specificity of aaRS in relation to computer simulations and energy calculations, which can be utilized to rationally design or predict the specificity of aaRS.

摘要

随着遗传密码扩展技术的进步,该领域正朝着纳入多种非标准氨基酸(ncAAs)的方向发展。氨酰-tRNA合成酶(aaRSs)对ncAAs的特异性是一个关键因素,因为工程化的aaRSs经常表现出多特异性,这使得多种ncAAs的精确掺入变得复杂。为应对这一挑战,预测结合亲和力可能会有所帮助。在本研究中,我们使用与4-叠氮基-L-苯丙氨酸(AzF)以及另外四种不同ncAAs的正交aaRS/tRNA对来表达超折叠绿色荧光蛋白(sfGFP)。实验结果显示了对O-甲基-L-酪氨酸以及AzF的特异性,并将这些结果与计算预测进行了比较。我们通过同源建模构建了对AzF具有特异性的突变aaRS结构,并与酪氨酸和五种ncAAs进行对接研究,随后进行分子动力学模拟。使用分子力学/泊松-玻尔兹曼表面积计算结合亲和力,重点关注非极性溶剂化项。虽然分析基于有限数量ncAAs的掺入,但空腔和色散项方法与实验数据显示出一致性,突出了其与表面积项方法相比的潜在实用性。这些发现增强了对aaRS在ncAA特异性方面与计算机模拟和能量计算关系的理解,可用于合理设计或预测aaRS的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/615150723aa5/pone.0316907.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/e83a56dd77db/pone.0316907.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/fe70c007b04b/pone.0316907.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/615150723aa5/pone.0316907.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/e83a56dd77db/pone.0316907.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/fe70c007b04b/pone.0316907.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daca/11723616/615150723aa5/pone.0316907.g005.jpg

相似文献

1
Predicting the polyspecificity of aminoacyl-tRNA synthetase for non-canonical amino acids using molecular dynamics simulation and MM/PBSA.利用分子动力学模拟和MM/PBSA预测氨酰-tRNA合成酶对非标准氨基酸的多特异性
PLoS One. 2025 Jan 10;20(1):e0316907. doi: 10.1371/journal.pone.0316907. eCollection 2025.
2
Engineered Aminoacyl-tRNA Synthetases with Improved Selectivity toward Noncanonical Amino Acids.工程化的对非天然氨基酸具有更高选择性的氨酰-tRNA 合成酶。
ACS Chem Biol. 2019 Apr 19;14(4):603-612. doi: 10.1021/acschembio.9b00088. Epub 2019 Apr 9.
3
Performance analysis of orthogonal pairs designed for an expanded eukaryotic genetic code.正交对设计用于扩展的真核遗传密码的性能分析。
PLoS One. 2012;7(4):e31992. doi: 10.1371/journal.pone.0031992. Epub 2012 Apr 6.
4
Exploring the substrate range of wild-type aminoacyl-tRNA synthetases.探索野生型氨酰-tRNA合成酶的底物范围。
Chembiochem. 2014 Aug 18;15(12):1805-1809. doi: 10.1002/cbic.201402083. Epub 2014 May 30.
5
Development of orthogonal aminoacyl-tRNA synthetase mutant for incorporating a non-canonical amino acid.用于掺入非天然氨基酸的正交氨酰-tRNA合成酶突变体的开发。
AMB Express. 2024 May 24;14(1):60. doi: 10.1186/s13568-024-01706-3.
6
Enzyme redesign and genetic code expansion.酶的重新设计与遗传密码扩展
Protein Eng Des Sel. 2023 Jan 21;36. doi: 10.1093/protein/gzad017.
7
High-Throughput Aminoacyl-tRNA Synthetase Engineering for Genetic Code Expansion in Yeast.高通量氨酰-tRNA 合成酶工程在酵母中的遗传密码扩展。
ACS Synth Biol. 2022 Jul 15;11(7):2284-2299. doi: 10.1021/acssynbio.1c00626. Epub 2022 Jul 6.
8
Plasticity and Constraints of tRNA Aminoacylation Define Directed Evolution of Aminoacyl-tRNA Synthetases.tRNA 氨酰化的可塑性和约束条件决定了氨酰-tRNA 合成酶的定向进化。
Int J Mol Sci. 2019 May 9;20(9):2294. doi: 10.3390/ijms20092294.
9
Directed evolution of aminoacyl-tRNA synthetases through hypermutation.通过超突变实现氨酰-tRNA合成酶的定向进化。
bioRxiv. 2024 Sep 27:2024.09.27.615507. doi: 10.1101/2024.09.27.615507.
10
An evolved pyrrolysyl-tRNA synthetase with polysubstrate specificity expands the toolbox for engineering enzymes with incorporation of noncanonical amino acids.一种具有多底物特异性的进化型吡咯赖氨酸 - tRNA合成酶扩展了用于通过掺入非天然氨基酸来工程化酶的工具库。
Bioresour Bioprocess. 2023 Dec 11;10(1):92. doi: 10.1186/s40643-023-00712-w.

本文引用的文献

1
Development of orthogonal aminoacyl-tRNA synthetase mutant for incorporating a non-canonical amino acid.用于掺入非天然氨基酸的正交氨酰-tRNA合成酶突变体的开发。
AMB Express. 2024 May 24;14(1):60. doi: 10.1186/s13568-024-01706-3.
2
AmberTools. AmberTools。
J Chem Inf Model. 2023 Oct 23;63(20):6183-6191. doi: 10.1021/acs.jcim.3c01153. Epub 2023 Oct 8.
3
Quintuply orthogonal pyrrolysyl-tRNA synthetase/tRNA pairs.五重正交吡咯赖氨酸-tRNA 合成酶/tRNA 对。
Nat Chem. 2023 Jul;15(7):948-959. doi: 10.1038/s41557-023-01232-y. Epub 2023 Jun 15.
4
Revisiting MMPBSA by Adoption of MC-Based Surface Area/Volume, ANI-ML Potentials, and Two-Valued Interior Dielectric Constant.重新审视 MMPBSA 通过采用基于 MC 的表面积/体积、ANI-ML 势能和双值内部分介电常数。
J Phys Chem B. 2023 May 25;127(20):4415-4429. doi: 10.1021/acs.jpcb.3c00834. Epub 2023 May 12.
5
Genetically programmed cell-based synthesis of non-natural peptide and depsipeptide macrocycles.基于基因编程的细胞合成非天然肽和去肽类大环。
Nat Chem. 2023 Jan;15(1):61-69. doi: 10.1038/s41557-022-01082-0. Epub 2022 Dec 22.
6
MM/PB(GB)SA benchmarks on soluble proteins and membrane proteins.关于可溶性蛋白质和膜蛋白的MM/PB(GB)SA基准测试。
Front Pharmacol. 2022 Dec 1;13:1018351. doi: 10.3389/fphar.2022.1018351. eCollection 2022.
7
PubChem 2023 update.PubChem 2023 更新。
Nucleic Acids Res. 2023 Jan 6;51(D1):D1373-D1380. doi: 10.1093/nar/gkac956.
8
A Photo-Crosslinking Approach to Identify Class II SUMO-1 Binders.一种用于鉴定II类SUMO-1结合蛋白的光交联方法。
Front Chem. 2022 May 30;10:900989. doi: 10.3389/fchem.2022.900989. eCollection 2022.
9
Molecular simulations of proteins: From simplified physical interactions to complex biological phenomena.蛋白质的分子模拟:从简化的物理相互作用到复杂的生物现象。
Biochim Biophys Acta Proteins Proteom. 2022 Mar 1;1870(3):140757. doi: 10.1016/j.bbapap.2022.140757. Epub 2022 Jan 17.
10
Bioorthogonal Chemistry and Its Applications.生物正交化学及其应用。
Bioconjug Chem. 2021 Dec 15;32(12):2457-2479. doi: 10.1021/acs.bioconjchem.1c00461. Epub 2021 Nov 30.