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用于确定病毒-宿主蛋白相互作用的下拉技术

Pull-Down Techniques for Determining Virus-Host Protein Interactions.

作者信息

Dai Jiaqi, Gong Zuxin, Li Xin, Liu Chenchen, Zheng Chunfu, Liu Gongguan

机构信息

College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, Jiangsu, China.

Department of Microbiology, Immunology & Infectious Diseases, University of Calgary, Calgary, AB, Canada.

出版信息

Methods Mol Biol. 2025;2940:133-140. doi: 10.1007/978-1-0716-4615-1_12.

DOI:10.1007/978-1-0716-4615-1_12
PMID:40515907
Abstract

Pull-down techniques are essential for identifying direct protein-protein interactions in vitro and play a pivotal role in the study of virus-host protein interactions. These methods rely on a bait protein immobilized on a solid support to capture target prey proteins, which are subsequently eluted and identified. In the context of viral infection research, pull-down techniques offer high specificity and low background interference, which are crucial for elucidating protein interaction networks and investigating cellular signaling pathways. This chapter provides a detailed description of the experimental methods for validating virus-host protein interactions through pull-down techniques, offers vital insights into the molecular mechanisms underlying viral infections, and serves as a cornerstone for drug development and therapeutic strategies.

摘要

下拉技术对于在体外鉴定直接的蛋白质-蛋白质相互作用至关重要,并且在病毒-宿主蛋白质相互作用的研究中发挥着关键作用。这些方法依赖于固定在固体支持物上的诱饵蛋白来捕获目标猎物蛋白,随后将其洗脱并鉴定。在病毒感染研究的背景下,下拉技术具有高特异性和低背景干扰,这对于阐明蛋白质相互作用网络和研究细胞信号通路至关重要。本章详细描述了通过下拉技术验证病毒-宿主蛋白质相互作用的实验方法,深入洞察了病毒感染背后的分子机制,并为药物开发和治疗策略奠定了基础。

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本文引用的文献

1
LLPS of FXR proteins drives replication organelle clustering for β-coronaviral proliferation.FXR 蛋白的液液相分离驱动复制细胞器聚集,从而促进 β 冠状病毒增殖。
J Cell Biol. 2024 Jun 3;223(6). doi: 10.1083/jcb.202309140. Epub 2024 Apr 8.
2
Utilization of SUMO Tag and Freeze-thawing Method for a High-level Expression and Solubilization of Recombinant Human Angiotensinconverting Enzyme 2 (rhACE2) Protein in .利用SUMO标签和冻融法在……中实现重组人血管紧张素转换酶2(rhACE2)蛋白的高水平表达和溶解
Protein Pept Lett. 2022;29(7):605-610. doi: 10.2174/0929866529666220715101357.
3
A molecular pore spans the double membrane of the coronavirus replication organelle.
一种分子孔跨越冠状病毒复制细胞器的双层膜。
Science. 2020 Sep 11;369(6509):1395-1398. doi: 10.1126/science.abd3629. Epub 2020 Aug 6.
4
Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor.SARS-CoV-2 刺突受体结合域与 ACE2 受体复合物的结构。
Nature. 2020 May;581(7807):215-220. doi: 10.1038/s41586-020-2180-5. Epub 2020 Mar 30.
5
SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor.严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)进入细胞依赖于 ACE2 和 TMPRSS2,可被一种临床验证的蛋白酶抑制剂所阻断。
Cell. 2020 Apr 16;181(2):271-280.e8. doi: 10.1016/j.cell.2020.02.052. Epub 2020 Mar 5.
6
Yeast Two-Hybrid Assay to Identify Interacting Proteins.酵母双杂交实验以鉴定相互作用蛋白。
Curr Protoc Protein Sci. 2019 Feb;95(1):e70. doi: 10.1002/cpps.70. Epub 2018 Aug 21.
7
Protein-Protein Interactions: Pull-Down Assays.蛋白质-蛋白质相互作用:下拉实验
Methods Mol Biol. 2017;1615:247-255. doi: 10.1007/978-1-4939-7033-9_20.
8
Purification of GST-Tagged Proteins.谷胱甘肽 S-转移酶(GST)标签蛋白的纯化
Methods Enzymol. 2015;559:127-39. doi: 10.1016/bs.mie.2014.11.005. Epub 2015 May 16.
9
Protein-protein interaction detection: methods and analysis.蛋白质-蛋白质相互作用检测:方法与分析
Int J Proteomics. 2014;2014:147648. doi: 10.1155/2014/147648. Epub 2014 Feb 17.
10
Fusion tags for protein solubility, purification and immunogenicity in Escherichia coli: the novel Fh8 system.用于大肠杆菌中蛋白质溶解性、纯化及免疫原性的融合标签:新型Fh8系统
Front Microbiol. 2014 Feb 19;5:63. doi: 10.3389/fmicb.2014.00063. eCollection 2014.