Ji Chang Hoon, Lee Min Ju, Kim Su Bin, Kwon Yong Tae
Cellular Degradation Biology Center and Department of Biomedical Sciences, College of Medicine, Seoul National University, Jongno-gu, Seoul, Republic of Korea.
AUTOTAC Bio Inc., Jongno-gu, Seoul, Republic of Korea.
Methods Mol Biol. 2023;2620:253-262. doi: 10.1007/978-1-0716-2942-0_27.
Characterizing and measuring the interactome of N-degrons and N-recognins are critical to the identification and verification of putative N-terminally arginylated native proteins and small-molecule chemicals that structurally and physiologically mimic the N-terminal arginine residue. This chapter focuses on in vitro and in vivo assays to confirm the putative interaction, and measure the binding affinity, between Nt-Arg-carrying natural (or Nt-Arg-mimicking synthetic) ligands and proteasomal or autophagic N-recognins carrying the UBR box or the ZZ domain. These methods, reagents, and conditions are applicable across a wide spectrum of different cell lines, primary cultures, and/or animal tissues, allowing for the qualitative analysis and quantitative measurement of the interaction of arginylated proteins and N-terminal arginine-mimicking chemical compounds to their respective N-recognins.
对N-端降解决定子和N-识别子的相互作用组进行表征和测量,对于鉴定和验证假定的N端精氨酸化天然蛋白质以及在结构和生理上模拟N端精氨酸残基的小分子化学物质至关重要。本章重点介绍体外和体内试验,以确认假定的相互作用,并测量携带Nt-Arg的天然(或模拟Nt-Arg的合成)配体与携带UBR盒或ZZ结构域的蛋白酶体或自噬N-识别子之间的结合亲和力。这些方法、试剂和条件适用于广泛的不同细胞系、原代培养物和/或动物组织,可对精氨酸化蛋白质和模拟N端精氨酸的化合物与其各自的N-识别子之间的相互作用进行定性分析和定量测量。