An active machine learning discovery platform for membrane-disrupting and pore-forming peptides
van Teijlingen, Alexander and Edwards, Daniel C. and Hu, Liao and Lilienkampf, Annamaria and Cockroft, Scott L. and Tuttle, Tell (2024) An active machine learning discovery platform for membrane-disrupting and pore-forming peptides. Physical Chemistry Chemical Physics, 26 (25). pp. 17745-17752. ISSN 1463-9084 (https://doi.org/10.1039/D4CP01404A)
Preview |
Text.
Filename: van-Teijlingen-etal-PCCP-2024-An-active-machine-learning-discovery-platform-for-membrane-disrupting.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
Membrane-disrupting and pore-forming peptides (PFPs) play a substantial role in bionanotechnology and can determine the life and death of cells. The control of chemical and ion transport through cell membranes is essential to maintaining concentration gradients. Likewise, the delivery of drugs and intracellular proteins aided by pore-forming agents is of interest in treating malfunctioning cells. Known PFPs tend to be up to 50 residues in length, which is commensurate with the thickness of a lipid bilayer. Accordingly, few short PFPs are known. Here we show that the discovery of PFPs can be accelerated via an active machine learning approach. The approach identified 71 potential PFPs from the 25.6 billion octapeptide sequence space; 13 sequences were tested experimentally, and all were found to have the predicted membrane-disrupting ability, with 1 forming highly stable pores. Experimental verification of the predicted pore-forming ability demonstrated that a range of short peptides can form pores in membranes, while the positioning and characteristics of residues that favour pore-forming behaviour were identified. This approach identified more ultrashort (8-residues, unmodified, non-cyclic) PFPs than previously known. We anticipate our findings and methodology will be useful in discovering new pore-forming and membrane-disrupting peptides for a range of applications from nanoreactors to therapeutics.
ORCID iDs
van Teijlingen, Alexander ORCID: https://orcid.org/0000-0002-3739-8943, Edwards, Daniel C., Hu, Liao, Lilienkampf, Annamaria, Cockroft, Scott L. and Tuttle, Tell;-
-
Item type: Article ID code: 89620 Dates: DateEvent7 July 2024Published30 May 2024Published Online30 May 2024AcceptedSubjects: Medicine > Biomedical engineering. Electronics. Instrumentation
Medicine > Pharmacy and materia medica > Pharmaceutical chemistryDepartment: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 17 Jun 2024 11:31 Last modified: 12 Dec 2024 15:31 URI: https://strathprints.strath.ac.uk/id/eprint/89620