De Novo Development of Mitochondria-Targeted Molecular Probes Targeting Pink1.

Pink1 backbone cyclization bioactive peptides mitochondria mitophagy molecular probes peptidomimetics protein-peptide interactions protein-protein interactions therapeutic peptides

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
28 May 2022
Historique:
received: 06 04 2022
revised: 23 05 2022
accepted: 25 05 2022
entrez: 10 6 2022
pubmed: 11 6 2022
medline: 14 6 2022
Statut: epublish

Résumé

Mitochondria play central roles in maintaining cellular metabolic homeostasis, cell survival and cell death, and generate most of the cell's energy. Mitochondria maintain their homeostasis by dynamic (fission and fusion) and quality control mechanisms, including mitophagy, the removal of damaged mitochondria that is mediated mainly by the Pink1/Parkin pathway. Pink1 is a serine/threonine kinase which regulates mitochondrial function, hitherto many molecular mechanisms underlying Pink1 activity in mitochondrial homeostasis and cell fate remain unknown. Peptides are vital biological mediators that demonstrate remarkable potency, selectivity, and low toxicity, yet they have two major limitations, low oral bioavailability and poor stability. Herein, we rationally designed a linear peptide that targets Pink1 and, using straightforward chemistry, we developed molecular probes with drug-like properties to further characterize Pink1. Initially, we conjugated a cell-penetrating peptide and a cross-linker to map Pink1's 3D structure and its interaction sites. Next, we conjugated a fluorescent dye for cell-imaging. Finally, we developed cyclic peptides with improved stability and binding affinity. Overall, we present a facile approach to converting a non-permeable linear peptide into a research tool possessing important properties for therapeutics. This is a general approach using straightforward chemistry that can be tailored for various applications by numerous laboratories.

Identifiants

pubmed: 35682755
pii: ijms23116076
doi: 10.3390/ijms23116076
pmc: PMC9181014
pii:
doi:

Substances chimiques

Molecular Probes 0
Ubiquitin-Protein Ligases EC 2.3.2.27
Protein Kinases EC 2.7.-
Protein Serine-Threonine Kinases EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Israel Science Foundation
ID : 935/20

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Auteurs

Shulamit Fluss Ben-Uliel (SF)

The Azrieli Faculty of Medicine in the Galilee, Bar-Ilan University, Safed 1311502, Israel.

Faten Habrat Zoabi (FH)

The Azrieli Faculty of Medicine in the Galilee, Bar-Ilan University, Safed 1311502, Israel.

Moriya Slavin (M)

Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.

Hadas Sibony-Benyamini (H)

The Azrieli Faculty of Medicine in the Galilee, Bar-Ilan University, Safed 1311502, Israel.

Nir Kalisman (N)

Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 9190401, Israel.

Nir Qvit (N)

The Azrieli Faculty of Medicine in the Galilee, Bar-Ilan University, Safed 1311502, Israel.

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Classifications MeSH