{"title":"Effects of lipid membranes on RNA catalytic activity and stability","authors":"Tomasz Czerniak, James Peter Saenz","doi":"10.1101/2024.08.31.610601","DOIUrl":null,"url":null,"abstract":"RNA plays crucial roles in cellular organization and metabolism, and modulating its activity is essential for maintaining cellular functions. RNA activity, involving both catalytic (ribozymes) and translation processes, is controlled via myriad mechanisms involving different binding partners such as proteins and smaller polar solutes. We previously reported that lipid membranes can directly interact with the artificial R3C ribozyme, changing its activity; however, the effect of lipids on naturally occurring ribozymes remains unknown. Here, we report that both catalytic activity and RNA integrity can be controlled by the presence of different lipid membranes. Lipid gel membranes decreased the activity of hepatitis delta virus (HDV) and increased the hammerhead (HH) ribozyme reaction yield. The presence of lipid liquid membrane lattices triggered RNA degradation, with greater degradation occurring in the single-stranded regions of RNA. The interplay between RNA activity and stability in the presence of different lipid membranes introduces multiple possibilities, where different combinations of ribozyme and lipid membrane composition could produce different effects on activity. Taken together, these observations support the hypothesis that the activity of both natural and artificial RNAs can be modulated by lipid membranes, which, in turn, contribute to the development of novel riboswitch-like molecules and lipid membrane-based RNA-biosensors.","PeriodicalId":501408,"journal":{"name":"bioRxiv - Synthetic Biology","volume":"30 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Synthetic Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.31.610601","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
RNA plays crucial roles in cellular organization and metabolism, and modulating its activity is essential for maintaining cellular functions. RNA activity, involving both catalytic (ribozymes) and translation processes, is controlled via myriad mechanisms involving different binding partners such as proteins and smaller polar solutes. We previously reported that lipid membranes can directly interact with the artificial R3C ribozyme, changing its activity; however, the effect of lipids on naturally occurring ribozymes remains unknown. Here, we report that both catalytic activity and RNA integrity can be controlled by the presence of different lipid membranes. Lipid gel membranes decreased the activity of hepatitis delta virus (HDV) and increased the hammerhead (HH) ribozyme reaction yield. The presence of lipid liquid membrane lattices triggered RNA degradation, with greater degradation occurring in the single-stranded regions of RNA. The interplay between RNA activity and stability in the presence of different lipid membranes introduces multiple possibilities, where different combinations of ribozyme and lipid membrane composition could produce different effects on activity. Taken together, these observations support the hypothesis that the activity of both natural and artificial RNAs can be modulated by lipid membranes, which, in turn, contribute to the development of novel riboswitch-like molecules and lipid membrane-based RNA-biosensors.