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Supramolecular Senolytics via Intracellular Oligomerization of Peptides in Response to Elevated Reactive Oxygen Species Levels in Aging Cells

  • Sangpil Kim
    Sangpil Kim
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
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  • Jae-Byoung Chae
    Jae-Byoung Chae
    Department of Ophthalmology, Konkuk University School of Medicine, Seoul 05029, Republic of Korea
  • Dohyun Kim
    Dohyun Kim
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    More by Dohyun Kim
  • Chul-Woo Park
    Chul-Woo Park
    Department of Ophthalmology, Konkuk University School of Medicine, Seoul 05029, Republic of Korea
  • Youjung Sim
    Youjung Sim
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    More by Youjung Sim
  • Hyungwoo Lee
    Hyungwoo Lee
    Department of Ophthalmology, Konkuk University School of Medicine, Seoul 05029, Republic of Korea
    More by Hyungwoo Lee
  • Gaeun Park
    Gaeun Park
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    More by Gaeun Park
  • Jaeeun Lee
    Jaeeun Lee
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    More by Jaeeun Lee
  • Seongho Hong
    Seongho Hong
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    More by Seongho Hong
  • Batakrishna Jana
    Batakrishna Jana
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
  • Chaekyu Kim
    Chaekyu Kim
    Fusion Biotechnology, Ulsan 44919, Republic of Korea
    More by Chaekyu Kim
  • Hyewon Chung*
    Hyewon Chung
    Department of Ophthalmology, Konkuk University School of Medicine, Seoul 05029, Republic of Korea
    *Email: [email protected]
    More by Hyewon Chung
  • , and 
  • Ja-Hyoung Ryu*
    Ja-Hyoung Ryu
    Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
    *Email: [email protected]
Cite this: J. Am. Chem. Soc. 2023, XXXX, XXX, XXX-XXX
Publication Date (Web):September 4, 2023
https://doi.org/10.1021/jacs.3c06898
© 2023 American Chemical Society

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    Abstract

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    Senolytics, which eliminate senescent cells from tissues, represent an emerging therapeutic strategy for various age-related diseases. Most senolytics target antiapoptotic proteins, which are overexpressed in senescent cells, limiting specificity and inducing severe side effects. To overcome these limitations, we constructed self-assembling senolytics targeting senescent cells with an intracellular oligomerization system. Intracellular aryl-dithiol-containing peptide oligomerization occurred only inside the mitochondria of senescent cells due to selective localization of the peptides by RGD-mediated cellular uptake into integrin αvβ3-overexpressed senescent cells and elevated levels of reactive oxygen species, which can be used as a chemical fuel for disulfide formation. This oligomerization results in an artificial protein-like nanoassembly with a stable α-helix secondary structure, which can disrupt the mitochondrial membrane via multivalent interactions because the mitochondrial membrane of senescent cells has weaker integrity than that of normal cells. These three specificities (integrin αvβ3, high ROS, and weak mitochondrial membrane integrity) of senescent cells work in combination; therefore, this intramitochondrial oligomerization system can selectively induce apoptosis of senescent cells without side effects on normal cells. Significant reductions in key senescence markers and amelioration of retinal degeneration were observed after elimination of the senescent retinal pigment epithelium by this peptide senolytic in an age-related macular degeneration mouse model and in aged mice, and this effect was accompanied by improved visual function. This system provides a strategy for the treatment of age-related diseases using supramolecular senolytics.

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/jacs.3c06898.

    • Materials and methods; mass analysis of synthetic molecules; mass analysis of oligomerization; observation of the nanostructure by DLS, CD, TEM, and SEM; HPLC analysis of monomers; fluorescence analysis for calculating the CAC of monomers; microscopy image of inducing senescence; western blot analysis of senescence markers; immunofluorescence of integrin αvβ3; CLSM image of mitochondrial localization; mass analysis of mitochondria isolated from solutions of senescent cells and normal cells; TEM images of senescent cells and normal cells with/without treatment of Mito-K2; dye release profile of model liposomes treated with monomers; CLSM image showing mitochondrial dysfunction; cell viability analysis of Mito-K1, Mito-K2, and Mito-K2-OH; time-dependent western blot analysis of senescent cells; flow cytometry of mitochondria-associated apoptosis; immunofluorescence of apolipoprotein E and Ki67; single-cell RNA sequencing of the retina; RNA fluorescence of RPE in an AMD model; in vivo experiment of Mito-K2; hematological/blood chemistry of Mito-K2 (PDF)

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