Greń Bartosz Ambroży, Dabrowski-Tumanski Pawel, Niemyska Wanda, Sulkowska Joanna Ida
Centre of New Technologies, University of Warsaw, 02-097 Warsaw, Poland.
Faculty of Physics, University of Warsaw, 02-093 Warsaw, Poland.
Polymers (Basel). 2021 Nov 18;13(22):3988. doi: 10.3390/polym13223988.
Complex lasso proteins are a recently identified class of biological compounds that are present in considerable fraction of proteins with disulfide bridges. In this work, we look at complex lasso proteins as a generalization of well-known cysteine knots and miniproteins (lasso peptides). In particular, we show that complex lasso proteins with the same crucial topological features-cysteine knots and lasso peptides-are antimicrobial proteins, which suggests that they act as a molecular plug. Based on an analysis of the stability of the lasso piercing residue, we also introduce a method to determine which lasso motif is potentially functional. Using this method, we show that the lasso motif in antimicrobial proteins, as well in that in cytokines, is functionally relevant. We also study the evolution of lasso motifs, their conservation, and the usefulness of the lasso fingerprint, which extracts all topologically non-triviality concerning covalent loops. The work is completed by the presentation of extensive statistics on complex lasso proteins to analyze, in particular, the strange propensity for "negative" piercings. We also identify 21 previously unknown complex lasso proteins with an ester and a thioester bridge.
复杂套索蛋白是最近发现的一类生物化合物,存在于相当一部分具有二硫键的蛋白质中。在这项工作中,我们将复杂套索蛋白视为著名的半胱氨酸结和小蛋白(套索肽)的推广。特别是,我们表明具有相同关键拓扑特征——半胱氨酸结和套索肽的复杂套索蛋白是抗菌蛋白,这表明它们起到分子塞的作用。基于对套索穿透残基稳定性的分析,我们还介绍了一种确定哪些套索基序可能具有功能的方法。使用这种方法,我们表明抗菌蛋白以及细胞因子中的套索基序在功能上是相关的。我们还研究了套索基序的进化、它们的保守性以及套索指纹的有用性,套索指纹提取了所有与共价环有关的拓扑非平凡性。通过展示关于复杂套索蛋白的大量统计数据来完成这项工作,特别是分析“负”穿透的奇怪倾向。我们还鉴定出21种先前未知的具有酯桥和硫酯桥的复杂套索蛋白。