Literature DB >> 34766305

Mitochondrial Targeting Probes, Drug Conjugates, and Gene Therapeutics.

Carmine Pasquale Cerrato1, Tove Kivijärvi2, Ülo Langel3,4.   

Abstract

Mitochondria represent an important drug target for many phatology, including neurodegeneration, metabolic disease, heart failure, ischemia-reperfusion injury, and cancer. Mitochondrial dysfunctions are caused by mutation in mitochondrial DNA or in nuclear genes encoding mitochondrial proteins. Cell-penetrating peptides (CPPs) have been employed to overcome biological barriers, target this organelle, and therapeuticaly restore mitochondrial functions. Here, we describe recent methods used to deliver oligonucleotides targeting mitochondrial protein by using mitochondrial penetrating peptides. In particular, we highlight recent advances of formulated peptides/oligonucleotides nanocomplexes as a proof-of-principle for pharmaceutical form of peptide-based therapeutics.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Intracellular delivery; Mitochondria; Nanocarriers; Nanoparticles; mitFects

Mesh:

Substances:

Year:  2022        PMID: 34766305     DOI: 10.1007/978-1-0716-1752-6_27

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  59 in total

Review 1.  Cell-penetrating peptides.

Authors:  M Lindgren; M Hällbrink; A Prochiantz; U Langel
Journal:  Trends Pharmacol Sci       Date:  2000-03       Impact factor: 14.819

Review 2.  Medium-sized peptides as built in carriers for biologically active compounds.

Authors:  Ferenc Hudecz; Zoltán Bánóczi; Gabriella Csík
Journal:  Med Res Rev       Date:  2005-11       Impact factor: 12.944

3.  Cellular uptake of an alpha-helical amphipathic model peptide with the potential to deliver polar compounds into the cell interior non-endocytically.

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Journal:  Biochim Biophys Acta       Date:  1998-11-11

4.  Cell penetration by transportan.

Authors:  M Pooga; M Hällbrink; M Zorko; U Langel
Journal:  FASEB J       Date:  1998-01       Impact factor: 5.191

5.  Intercellular trafficking and protein delivery by a herpesvirus structural protein.

Authors:  G Elliott; P O'Hare
Journal:  Cell       Date:  1997-01-24       Impact factor: 41.582

6.  Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator protein.

Authors:  M Green; P M Loewenstein
Journal:  Cell       Date:  1988-12-23       Impact factor: 41.582

7.  A truncated HIV-1 Tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus.

Authors:  E Vivès; P Brodin; B Lebleu
Journal:  J Biol Chem       Date:  1997-06-20       Impact factor: 5.157

8.  The third helix of the Antennapedia homeodomain translocates through biological membranes.

Authors:  D Derossi; A H Joliot; G Chassaing; A Prochiantz
Journal:  J Biol Chem       Date:  1994-04-08       Impact factor: 5.157

9.  Cellular uptake of the tat protein from human immunodeficiency virus.

Authors:  A D Frankel; C O Pabo
Journal:  Cell       Date:  1988-12-23       Impact factor: 41.582

10.  Arginine-rich peptides. An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery.

Authors:  S Futaki; T Suzuki; W Ohashi; T Yagami; S Tanaka; K Ueda; Y Sugiura
Journal:  J Biol Chem       Date:  2000-11-17       Impact factor: 5.157

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