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  Amphiphiles formed from synthetic DNA-nanomotifs mimic the stepwise dispersal of transcriptional clusters in the cell nucleus

Tschurikow, X., Gadzekpo, A., Tran, M. P., Chatterjee, R., Sobucki, M., Zaburdaev, V., et al. (2023). Amphiphiles formed from synthetic DNA-nanomotifs mimic the stepwise dispersal of transcriptional clusters in the cell nucleus. Nano Letters, 23(17), 7815-7824. doi:10.1021/acs.nanolett.3c01301.

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 Creators:
Tschurikow, Xenia, Author
Gadzekpo, Aaron, Author
Tran, Mai P.1, Author           
Chatterjee, Rakesh, Author
Sobucki, Marcel, Author
Zaburdaev, Vasily, Author
Göpfrich, Kerstin2, Author           
Hilbert, Lennart, Author
Affiliations:
1Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              
2Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society, ou_2364731              

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Free keywords: DNA nanotechnology, Cell nucleus, Synthetic biology, Phase separation, Biomolecular condensates, Microemulsion
 Abstract: Stem cells exhibit prominent clusters controlling the transcription of genes into RNA. These clusters form by a phase-separation mechanism, and their size and shape are controlled via an amphiphilic effect of transcribed genes. Here, we construct amphiphile-nanomotifs purely from DNA, and we achieve similar size and shape control for phase-separated droplets formed from fully synthetic, self-interacting DNA-nanomotifs. Increasing amphiphile concentrations induce rounding of droplets, prevent droplet fusion, and, at high concentrations, cause full dispersal of droplets. Super-resolution microscopy data obtained from zebrafish embryo stem cells reveal a comparable transition for transcriptional clusters with increasing transcription levels. Brownian dynamics and lattice simulations further confirm that the addition of amphiphilic particles is sufficient to explain the observed changes in shape and size. Our work reproduces key aspects of transcriptional cluster formation in biological cells using relatively simple DNA sequence-programmable nanostructures, opening novel ways to control the mesoscopic organization of synthetic nanomaterials.

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Language(s): eng - English
 Dates: 2023-07-282023-04-062023-08-162023-09-13
 Publication Status: Issued
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acs.nanolett.3c01301
 Degree: -

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Title: Nano Letters
  Abbreviation : Nano Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 23 (17) Sequence Number: - Start / End Page: 7815 - 7824 Identifier: ISSN: 1530-6984
CoNE: https://pure.mpg.de/cone/journals/resource/110978984570403