Mitochondrion-Targeting Peptides and Peptidomimetics: Recent Progress and Design Principles
Abstract
Mitochondria are multifunctional subcellular organelles whose operations encompass energy production, signal transduction, and metabolic regulation. Given their wide range of roles, they have been studied extensively as a potential therapeutic target for the treatment of various diseases, including cancer, diabetes, and neurodegenerative diseases. Mitochondrion-mediated pathways have been identified as promising targets in the context of these diseases. However, the delivery of specific probes and drugs to the mitochondria is one of the major problems that remains to be solved. Over the past decade, much effort has been devoted to developing mitochondrion-targeted delivery methods based on the membrane characteristics and the protein import machinery of mitochondria. While various methods utilizing small molecules to polymeric particles have been introduced, it is notable that many of these compounds share common structural elements and physicochemical properties for optimal selectivity and efficiency. In this Perspective, we will review the most recently developed mitochondrion-targeting peptides and peptidomimetics to outline the key aspects of structural requirements and design principles. We will also discuss successful and potential applications of mitochondrial delivery to assess opportunities and challenges in the targeting of mitochondria.
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Targeting peptides such as Szeto-Schiller peptide and mitochondria-penetrating peptide facilitate peptide-tagged target compounds to localize within the mitochondria.
“Moreover, targeting peptides such as Szeto-Schiller peptide and mitochondria-penetrating peptide facilitate peptide-tagged target compounds to localize within the mitochondria (26, 27).”
From Recent Progress in Research on Mitochondrion-Targeted Antifungal Drugs: a Review (2023) · cites this paper as [27]
Cites
Targeting multidrug resistance in cancer
Szakács, G., Paterson, J. K., Ludwig, J. A., Booth-Genthe, C., & Gottesman, M. M. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd1984 · Cited by 3,609 · see citing works
The mitochondrial basis of aging
Sun, N., Youle, R. J., & Finkel, T. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.01.028 · Cited by 1,441 · see citing works
Mitochondrial DNA in innate immune responses and inflammatory pathology
West, A. P., & Shadel, G. S. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.21 · Cited by 1,115 · see citing works
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Recent Progress in Research on Mitochondrion-Targeted Antifungal Drugs: a Review
Qin, Y., Wang, J., Lv, Q., & Han, B. (2023) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00003-23 · Cited by 38 · see citing works
“Moreover, targeting peptides such as Szeto-Schiller peptide and mitochondria-penetrating peptide facilitate peptide-tagged target compounds to localize within the mitochondria (26, 27).”
Background
- Authors
- Kim, S., Nam, H. Y., Lee, J., & Seo, J.
- Affiliations
- Gwangju Institute of Science and Technology (KR)
- Department of Global Medical Science, Sungshin University, Seoul 01133, Republic of Korea
- Corresponding author
- Lee, Jiyoun
- Seo, Jiwon
- Venue
- Biochemistry
- Publisher
- American Chemical Society (ACS)
- Published
- 2019-11-07
- Volume
- 59
- Issue
- 3
- Pages
- 270-284
- ISSN
- 0006-2960 (ISSN-L)
- 1520-4995
- OpenAlex
- W2986659799
- Cited by
- 75
- References
- 3
- Citations by year
- 2026: 13 · 2025: 15 · 2024: 8 · 2023: 9 · 2022: 10 · 2021: 16 · 2020: 4
- FWCI
- 2.48
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Research Foundation of Korea (NRF-2018M3D1A1052659, NRF-2018R1A2B6007535, NRF-2018R1D1A1B07042846)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chemical Synthesis and Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- mitochondria, peptidomimetics, mitochondrial delivery, drug delivery, cancer therapy, neurodegenerative diseases, diabetes mellitus, structural design principles
- MeSH terms
- Humans, Mitochondria, Neoplasms, Peptides, Signal Transduction, Drug Delivery Systems, Protein Transport, Small Molecule Libraries, Peptidomimetics
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