bioRxivCell BiologyPreprint
Lipoproteins modulate the uptake and biological functionof cationic cell-penetrating peptides across the animal lineage.
Sovanny R. TayloriD, Temilade V. Oluwasesin, Muthu Raj SalaikumaraniD, Borna NovakiD, Adam BrineriD, Roshan Ailani, Pilar I. Andrade, Paulo L. OnuchiciD, Olivia M. S. CarmoiD, Garam KımiD, Jacob A. BlumiD, Mason Galliver, Catherine Stuart, Nicolás MéndeziD, Vedant Patel, Guo-Teng LiangiD, Ronan O’Connell, Mohammad Majharul IslamiD, Zeinab KashaniasliD, María José VillariD, Yingqiong Cao, Xi‐Lei ZengiD, Lucas Carvalho Porta, Haoyun YangiD, Gabe Hohensee, , Steven BoeynaemsiD
Abstract
Cationic cell-penetrating peptides (+CPPs) are pervasive killer peptides produced by all animals and found in innate immune systems, venoms and neurodegenerative diseases. Despite their ubiquity, the mechanisms underlying their uptake remain opaque and intensely debated. Here, we interrogate +CPPs spanning 600 million years of animal evolution and identify endocytosis as a conserved/convergent uptake mechanism across cell types and organisms, at physiological concentrations. By combining multiplex imaging, genetic screening, cryo-electron tomography, and biophysical methods, we uncover that +CPPs seemingly universally enter eukaryote cells via 'hitchhiking' on lipoproteins. We further show that the interaction of +CPPs with lipoproteins modulates their antimicrobial function. Combined, our findings establish a unified molecular framework describing a pan-eukaryote cell penetrance mechanism. As hyperlipidemia is a common comorbidity, our findings have direct implications for human health. Lastly, the insights gleaned from this work highlight design principles that may inform the future engineering of peptide-based therapeutics and delivery vehicles.
- organism: human
- organism: mouse
- organism: zebrafish
- assay: proteomics
- assay: imaging
- assay: cryo-EM
- research focus: host-pathogen & immune response
- research focus: cell signaling & trafficking
- research focus: cell type annotation
- approach: experimental assay
- approach: microscopy & imaging analysis
- approach: biophysical modeling
- Citations
- 0
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