Beckman Institute, University of Illinois, Urbana-Champaign, Urbana, Illinois, USA; Department of Molecular and Integrative Physiology, University of Illinois, Urbana-Champaign, Urbana, Illinois, USA; Institute for Genomic Biology, University of Illinois, Urbana-Champaign, Urbana, Illinois, USA.
Beckman Institute, University of Illinois, Urbana-Champaign, Urbana, Illinois, USA; Department of Molecular and Integrative Physiology, University of Illinois, Urbana-Champaign, Urbana, Illinois, USA.
J Biol Chem. 2024 Jul;300(7):107458. doi: 10.1016/j.jbc.2024.107458. Epub 2024 Jun 8.
The function of endogenous cell-cell signaling peptides relies on their interactions with cognate receptors, which in turn are influenced by the peptides' structures, necessitating a comprehensive understanding of the suite of post-translational modifications of the peptide. Herein, we report the initial characterization of putative peptide isomerase enzymes extracted from R. norvegicus, A. californica, and B. taurus tissues. These enzymes are both tissue and substrate-specific across all three organisms. Notably, the lungs of the mammalian species, and the central nervous system of the mollusk displayed the highest isomerase activity among the examined tissues. In vitro enzymatic conversion was observed for several endogenous peptides, such as the tetrapeptide GFFD in A. californica, and mammalian neuropeptide FF in R. norvegicus and B. taurus. To understand their mode of action, we explored the effects of several inhibitors on these enzymes, which suggest common active site residues. While further characterization of these enzymes is required, the investigations emphasize a widespread and overlooked enzyme activity related to the creation of bioactive peptides.
内源性细胞间信号肽的功能依赖于它们与同源受体的相互作用,而受体又受到肽结构的影响,因此需要全面了解肽的一系列翻译后修饰。在此,我们报告了从 R. norvegicus、A. californica 和 B. taurus 组织中提取的假定肽异构酶的初步特征。这些酶在所有三种生物中都是组织和底物特异性的。值得注意的是,在检查的组织中,哺乳动物的肺和软体动物的中枢神经系统显示出最高的异构酶活性。在体外酶促转化观察到几种内源性肽,如 A. californica 中的四肽 GFFD 和 R. norvegicus 和 B. taurus 中的哺乳动物神经肽 FF。为了了解它们的作用机制,我们研究了几种抑制剂对这些酶的影响,这些抑制剂提示了常见的活性位点残基。虽然需要进一步表征这些酶,但这些研究强调了与生物活性肽产生相关的广泛而被忽视的酶活性。