Programmable artificial RNA condensates in mammalian cells

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Authors: Shiyi Li, Yuna Kim, Kevin Wang, Eric John Payson, Anli A Tang, Maria Villalba Nieto, Dino Osmanović, Madison Yang, Diego Dilao, Alexandra Bermudez, Wen Xiao, Melody M H Li
+4 more Neil Y C Lin, Kathrin Plath, Douglas L. Black, Elisa Franco
Cited by: 5
References: 58

Abstract

Artificial biomolecular condensates have emerged as powerful tools for controlling cellular behaviour. Here we introduce a method to build artificial condensates within living mammalian cells by designing modular RNA motifs composed of a single short RNA strand. These condensates emerge spontaneously, creating RNA-rich compartments that remain separated from their surrounding environment. The RNA sequences include stem-loop domains that fold as the RNA is transcribed, and then condense in the nucleus and cytoplasm through loop-loop interactions. These sequences can be optimized and diversified, enabling the generation of distinct, non-mixing condensate populations and the programmable control of their subcellular localization. The RNA motifs can also be modified to recruit small molecules, proteins and RNA molecules in a sequence-specific manner to the RNA-rich phase. By introducing RNA linkers, we can build condensates with multiple subcompartments, whose organization can be controlled by tuning the linker stoichiometry. These artificial condensates provide a versatile platform for studying and manipulating molecular functions inside living cells.

Fields of Study & Subjects

Advanced biosensing and bioanalysis techniques RNA and protein synthesis mechanisms Nanopore and Nanochannel Transport Studies

Publication details

Journal / source
Nature Nanotechnology
Publisher
Springer Science and Business Media LLC
Volume
21
Issue
6
Pages
821–830
Publication date
29 April 2026
Language
EN