Department of Computing and Mathematical Sciences, California Institute of Technology, Pasadena, CA, USA.
Department of Bioengineering, University of California, Los Angeles, CA, USA.
Nat Commun. 2024 Jul 30;15(1):6244. doi: 10.1038/s41467-024-50003-x.
Recent discoveries in biology have highlighted the importance of protein and RNA-based condensates as an alternative to classical membrane-bound organelles. Here, we demonstrate the design of pure RNA condensates from nanostructured, star-shaped RNA motifs. We generate condensates using two different RNA nanostar architectures: multi-stranded nanostars whose binding interactions are programmed via linear overhangs, and single-stranded nanostars whose interactions are programmed via kissing loops. Through systematic sequence design, we demonstrate that both architectures can produce orthogonal (distinct and immiscible) condensates, which can be individually tracked via fluorogenic aptamers. We also show that aptamers make it possible to recruit peptides and proteins to the condensates with high specificity. Successful co-transcriptional formation of condensates from single-stranded nanostars suggests that they may be genetically encoded and produced in living cells. We provide a library of orthogonal RNA condensates that can be modularly customized and offer a route toward creating systems of functional artificial organelles for the task of compartmentalizing molecules and biochemical reactions.
生物学的最新发现强调了蛋白质和基于 RNA 的凝聚物作为替代经典膜结合细胞器的重要性。在这里,我们展示了从纳米结构的星形 RNA 基序设计纯 RNA 凝聚物。我们使用两种不同的 RNA 纳米星结构生成凝聚物:通过线性突出部分编程结合相互作用的多链纳米星,以及通过亲吻环编程相互作用的单链纳米星。通过系统的序列设计,我们证明了这两种结构都可以产生正交(不同且不混溶)的凝聚物,这些凝聚物可以通过荧光适体进行单独追踪。我们还表明,适体能以高特异性将肽和蛋白质募集到凝聚物中。从单链纳米星转录共形成凝聚物的成功表明,它们可能是遗传编码的,并可以在活细胞中产生。我们提供了一组正交的 RNA 凝聚物,这些凝聚物可以进行模块化定制,并为创建用于分隔分子和生化反应的功能性人工细胞器系统提供了一种途径。