Engineering ssRNA tile filaments for (dis)assembly and membrane binding

Journal Article (2024)
Author(s)

N. De Franceschi (BN/Cees Dekker Lab)

B. Hoogenberg (BN/Cees Dekker Lab)

A.J. Katan (TU Delft - QN/Afdelingsbureau)

C. Dekker (BN/Cees Dekker Lab)

Research Group
QN/Afdelingsbureau
DOI related publication
https://doi.org/10.1039/D3NR06423A
More Info
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Publication Year
2024
Language
English
Research Group
QN/Afdelingsbureau
Journal title
Nanoscale
Issue number
9
Volume number
16
Article number
d3nr06423a
Pages (from-to)
4890-4899
Downloads counter
255
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Abstract

Cytoskeletal protein filaments such as actin and microtubules confer mechanical support to cells and facilitate many cellular functions such as motility and division. Recent years have witnessed the development of a variety of molecular scaffolds that mimic such filaments. Indeed, filaments that are programmable and compatible with biological systems may prove useful in studying or substituting such proteins. Here, we explore the use of ssRNA tiles to build and modify filaments in vitro. We engineer a number of functionalities that are crucial to the function of natural proteins filaments into the ssRNA tiles, including the abilities to assemble or disassemble filaments, to tune the filament stiffness, to induce membrane binding, and to bind proteins. This work paves the way for building dynamic cytoskeleton-mimicking systems made out of rationally designed ssRNA tiles that can be transcribed in natural or synthetic cells.