Literature DB >> 33922379

Peptides to Tackle Leishmaniasis: Current Status and Future Directions.

Alberto A Robles-Loaiza1, Edgar A Pinos-Tamayo1, Bruno Mendes2, Cátia Teixeira3, Cláudia Alves3, Paula Gomes3, José R Almeida1.   

Abstract

Peptide-based drugs are an attractive class of therapeutic agents, recently recognized by the pharmaceutical industry. These molecules are currently being used in the development of innovative therapies for diverse health conditions, including tropical diseases such as leishmaniasis. Despite its socioeconomic influence on public health, leishmaniasis remains long-neglected and categorized as a poverty-related disease, with limited treatment options. Peptides with antileishmanial effects encountered to date are a structurally heterogeneous group, which can be found in different natural sources-amphibians, reptiles, insects, bacteria, marine organisms, mammals, plants, and others-or inspired by natural toxins or proteins. This review details the biochemical and structural characteristics of over one hundred peptides and their potential use as molecular frameworks for the design of antileishmanial drug leads. Additionally, we detail the main chemical modifications or substitutions of amino acid residues carried out in the peptide sequence, and their implications in the development of antileishmanial candidates for clinical trials. Our bibliographic research highlights that the action of leishmanicidal peptides has been evaluated mainly using in vitro assays, with a special emphasis on the promastigote stage. In light of these findings, and considering the advances in the successful application of peptides in leishmaniasis chemotherapy, possible approaches and future directions are discussed here.

Entities:  

Keywords:  Leishmania spp.; amastigote; drug discovery; peptides; promastigote

Mesh:

Substances:

Year:  2021        PMID: 33922379     DOI: 10.3390/ijms22094400

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  83 in total

1.  N-terminal fatty acid substitution increases the leishmanicidal activity of CA(1-7)M(2-9), a cecropin-melittin hybrid peptide.

Authors:  C Chicharro; C Granata; R Lozano; D Andreu; L Rivas
Journal:  Antimicrob Agents Chemother       Date:  2001-09       Impact factor: 5.191

2.  Dissection of antibacterial and toxic activity of melittin: a leucine zipper motif plays a crucial role in determining its hemolytic activity but not antibacterial activity.

Authors:  Neeta Asthana; Sharada Prasad Yadav; Jimut Kanti Ghosh
Journal:  J Biol Chem       Date:  2004-10-08       Impact factor: 5.157

3.  Antimicrobial peptides isolated from Phyllomedusa nordestina (Amphibia) alter the permeability of plasma membrane of Leishmania and Trypanosoma cruzi.

Authors:  Erika Gracielle Pinto; Daniel C Pimenta; Marta Maria Antoniazzi; Carlos Jared; Andre Gustavo Tempone
Journal:  Exp Parasitol       Date:  2013-10-08       Impact factor: 2.011

Review 4.  Designing and optimizing new antimicrobial peptides: all targets are not the same.

Authors:  Adriana Barreto-Santamaría; Manuel E Patarroyo; Hernando Curtidor
Journal:  Crit Rev Clin Lab Sci       Date:  2019-08-09       Impact factor: 6.250

5.  Trypanocidal and leishmanicidal activities of different antimicrobial peptides (AMPs) isolated from aquatic animals.

Authors:  S E Löfgren; L C Miletti; M Steindel; E Bachère; M A Barracco
Journal:  Exp Parasitol       Date:  2007-08-15       Impact factor: 2.011

6.  Kahalalide F, an antitumor depsipeptide in clinical trials, and its analogues as effective antileishmanial agents.

Authors:  Luis J Cruz; Juan R Luque-Ortega; Luis Rivas; Fernando Albericio
Journal:  Mol Pharm       Date:  2009 May-Jun       Impact factor: 4.939

7.  Comparative study of different forms of Jellein antimicrobial peptide on Leishmania parasite.

Authors:  Farnaz Zahedifard; Hyeryon Lee; Joo Hwan No; Mona Salimi; Negar Seyed; Ahmad Asoodeh; Sima Rafati
Journal:  Exp Parasitol       Date:  2019-12-17       Impact factor: 2.011

8.  The role of phosphoglycans in the susceptibility of Leishmania mexicana to the temporin family of anti-microbial peptides.

Authors:  Gabriela A Eggimann; Kathryn Sweeney; Hannah L Bolt; Neshat Rozatian; Steven L Cobb; Paul W Denny
Journal:  Molecules       Date:  2015-02-06       Impact factor: 4.411

Review 9.  The Geographical Distribution of Cutaneous Leishmaniasis Causative Agents in Iran and Its Neighboring Countries, A Review.

Authors:  Mohammad Amin Ghatee; Walter R Taylor; Mehdi Karamian
Journal:  Front Public Health       Date:  2020-02-18

Review 10.  From antimicrobial to anticancer peptides. A review.

Authors:  Diana Gaspar; A Salomé Veiga; Miguel A R B Castanho
Journal:  Front Microbiol       Date:  2013-10-01       Impact factor: 5.640

View more
  4 in total

1.  Lessons from a Single Amino Acid Substitution: Anticancer and Antibacterial Properties of Two Phospholipase A2-Derived Peptides.

Authors:  José R Almeida; Bruno Mendes; Marcelo Lancellotti; Gilberto C Franchi; Óscar Passos; Maria J Ramos; Pedro A Fernandes; Cláudia Alves; Nuno Vale; Paula Gomes; Saulo L da Silva
Journal:  Curr Issues Mol Biol       Date:  2021-12-22       Impact factor: 2.976

Review 2.  Bioactive Antimicrobial Peptides: A New Weapon to Counteract Zoonosis.

Authors:  Luisa Zupin; Carlos André Dos Santos-Silva; Aya R Hamad Al Mughrbi; Livia Maria Batista Vilela; Ana Maria Benko-Iseppon; Sergio Crovella
Journal:  Microorganisms       Date:  2022-08-07

Review 3.  Metabolic Pathways of Leishmania Parasite: Source of Pertinent Drug Targets and Potent Drug Candidates.

Authors:  Surbhi Jain; Utkarsha Sahu; Awanish Kumar; Prashant Khare
Journal:  Pharmaceutics       Date:  2022-07-30       Impact factor: 6.525

Review 4.  Traditional and Computational Screening of Non-Toxic Peptides and Approaches to Improving Selectivity.

Authors:  Alberto A Robles-Loaiza; Edgar A Pinos-Tamayo; Bruno Mendes; Josselyn A Ortega-Pila; Carolina Proaño-Bolaños; Fabien Plisson; Cátia Teixeira; Paula Gomes; José R Almeida
Journal:  Pharmaceuticals (Basel)       Date:  2022-03-08
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.