De novo designed peptides for cellular delivery and subcellular localisation

Guto G. Rhys, Jessica A. Cross, William M. Dawson, Harry F. Thompson, Sooruban Shanmugaratnam, Nigel J. Savery, Mark P. Dodding, Birte Höcker*, Derek N. Woolfson*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

24 Citations (Scopus)
311 Downloads (Pure)

Abstract

Increasingly, it is possible to design peptide and protein assemblies de novo from first principles or computationally. This approach provides new routes to functional synthetic polypeptides, including designs to target and bind proteins of interest. Much of this work has been developed in vitro. Therefore, a challenge is to deliver de novo polypeptides efficiently to sites of action within cells. Here we describe the design, characterisation, intracellular delivery, and subcellular localisation of a de novo synthetic peptide system. This system comprises a dual-function basic peptide, programmed both for cell penetration and target binding, and a complementary acidic peptide that can be fused to proteins of interest and introduced into cells using synthetic DNA. The designs are characterised in vitro using biophysical methods and X-ray crystallography. The utility of the system for delivery into mammalian cells and subcellular targeting is demonstrated by marking organelles and actively engaging functional protein complexes.
Original languageEnglish
Pages (from-to)999-1004
Number of pages6
JournalNature Chemical Biology
Volume18
Issue number9
Early online date14 Jul 2022
DOIs
Publication statusPublished - 1 Sept 2022

Bibliographical note

Funding Information:
G.G.R. is supported by the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement number 88899. J.A.C. is supported by the EPSRC-funded Bristol Centre for Doctoral Training in Chemical Synthesis (EP/G036764/1). H.F.T. is supported by the EPSRC- and BBSRC-funded Centre for Doctoral Training in Synthetic Biology (EP/L016494/1). M.P.D. is a Lister Institute of Preventative Medicine Fellow and work in his lab is supported by BBSRC (BB/S000917/1). We thank the University of Bristol School of Chemistry Mass Spectrometry Facility for access to the EPSRC-funded Bruker Ultraflex MALDI–TOF instrument (EP/K03927X/1), the BBSRC-funded BrisSynBio centre for access to peptide synthesis and a plate reader (BB/L01386X/1), and the Wolfson Bioimaging Facility for their assistance in this work. B.H. acknowledges financial support and allocation of beamtime by HZB and we thank the beamline staff at BESSY for assistance.

Funding Information:
G.G.R. is supported by the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement number 88899. J.A.C. is supported by the EPSRC-funded Bristol Centre for Doctoral Training in Chemical Synthesis (EP/G036764/1). H.F.T. is supported by the EPSRC- and BBSRC-funded Centre for Doctoral Training in Synthetic Biology (EP/L016494/1). M.P.D. is a Lister Institute of Preventative Medicine Fellow and work in his lab is supported by BBSRC (BB/S000917/1). We thank the University of Bristol School of Chemistry Mass Spectrometry Facility for access to the EPSRC-funded Bruker Ultraflex MALDI–TOF instrument (EP/K03927X/1), the BBSRC-funded BrisSynBio centre for access to peptide synthesis and a plate reader (BB/L01386X/1), and the Wolfson Bioimaging Facility for their assistance in this work. B.H. acknowledges financial support and allocation of beamtime by HZB and we thank the beamline staff at BESSY for assistance.

Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature America, Inc.

Research Groups and Themes

  • Bristol BioDesign Institute
  • BCS and TECS CDTs

Keywords

  • synthetic biology

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