Disulfide cross-linked redox-sensitive peptide condensates are efficient cell delivery vehicles of molecular cargo

Biomolecular condensates (BCs) are phase-separated viscoelastic hubs within demixed solutions enriched in proteins and nucleic acids. Such condensates, also called membraneless organelles, are increasingly observed in cells and serve as transient hubs for spatial organization and compartmentalization of biomolecules. Along with the transiency of formation and dissolution, their ability to sequester molecules has inspired us to develop BCs as potential vehicles to transport and deliver molecular cargo. We recently reported the design of disulfide bond cross-linked phase-separating peptide (PSP) condensates that spontaneously dissolve in reducing conditions. Based on the premise that the highly reducing cytoplasm could dissolve PSP condensates and release partitioned cargo, here, we demonstrate the ability of PSP condensates to deliver molecular cargo to the cytoplasm of HeLa cells. We show that PSP condensates deliver a variety of cargos that differ in their sizes and chemistries, including small molecules, peptides, GFP (31 kDa), DNA (1.7 kbp), and mRNA. The transfection efficiencies of PSP condensates for delivering DNA and mRNA were also significantly greater than those of a commercial transfection agent. With room to tailor the condensate properties based on cargo and cell types, these results showcase the potential of disulfide-cross-linked PSPs as effective and customizable cellular delivery vehicles, filling a critical demand gap for such delivery systems.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-10-08
DOI
https://doi.org/10.1073/pnas.2515427122
Citations
2
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
1.61
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article

Disulfide cross-linked redox-sensitive peptide condensates are efficient cell delivery vehicles of molecular cargo

Fengwei Bai, Malay Mondal, Tristan D. Clemons, Sabin Shrestha et al.
2 citations
Proceedings of the National Academy of Sciences
RNA Interference and Gene Delivery
1.61
article

Disulfide cross-linked redox-sensitive peptide condensates are efficient cell delivery vehicles of molecular cargo

Fengwei Bai, Malay Mondal, Tristan D. Clemons, Sabin Shrestha, Vijayaraghavan Rangachari, Faqing Huang, Sufia Karim, Windfield S. Swetman, Alice Davis
article en
2 citations

Abstract

Biomolecular condensates (BCs) are phase-separated viscoelastic hubs within demixed solutions enriched in proteins and nucleic acids. Such condensates, also called membraneless organelles, are increasingly observed in cells and serve as transient hubs for spatial organization and compartmentalization of biomolecules. Along with the transiency of formation and dissolution, their ability to sequester molecules has inspired us to develop BCs as potential vehicles to transport and deliver molecular cargo. We recently reported the design of disulfide bond cross-linked phase-separating peptide (PSP) condensates that spontaneously dissolve in reducing conditions. Based on the premise that the highly reducing cytoplasm could dissolve PSP condensates and release partitioned cargo, here, we demonstrate the ability of PSP condensates to deliver molecular cargo to the cytoplasm of HeLa cells. We show that PSP condensates deliver a variety of cargos that differ in their sizes and chemistries, including small molecules, peptides, GFP (31 kDa), DNA (1.7 kbp), and mRNA. The transfection efficiencies of PSP condensates for delivering DNA and mRNA were also significantly greater than those of a commercial transfection agent. With room to tailor the condensate properties based on cargo and cell types, these results showcase the potential of disulfide-cross-linked PSPs as effective and customizable cellular delivery vehicles, filling a critical demand gap for such delivery systems.

Proceedings of the National Academy of SciencesVol. 122(41)
University of Southern Mississippi (US)
Openalex Percentile: Top 14%
RNA Interference and Gene Delivery
1.61
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