Strategies developed to overcome limitations in the use of peptides
Limitation | Strategy | References |
---|---|---|
Improve stability by preventing proteolysis | Use of modified amino acids such as D amino acids, methylated amino acids, and beta-amino acids among others | [20, 81, 82] |
Improve stability and activity by preserving secondary structure | Use of hydrogen bond surrogates (HBS), generation of covalent bonds, cyclic peptides | [81–83] |
Membrane penetration | Conjugation with lipids or biocompatible polymers | [20] |
Delivery systems to enhance activity and stability | Use of nanotechnologyFunctionalized surfacesNucleic acids systemsHydrogels and scaffolds | [84–86] |
Cost of synthesis | New strategies towards circular economyProduction as recombinants | [23, 87] |
The authors thank all the students who were part of this journey and who have supported each of the reported publications.
CC: Conceptualization, Data Curation, Writing—original draft, Writing—review & editing, Validation, Visualization, Funding acquisition. PS: Writing—review & editing. CA: Data curation, Writing—original draft, Writing—review & editing, Validation. LM and SM: Writing—review & editing. FA: Writing—review & editing, Validation. FG: Conceptualization, Data curation, Validation, Project administration.
Fernando Albericio, the Editor-in-Chief and a Guest Editor of Exploration of Drug Science, and Fanny Guzmán, a Guest Editor of Exploration of Drug Science, had no involvement in the decision-making or the review process of this manuscript. The other authors declare no conflicts of interest.
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FG received financial support from ANID Fondecyt [1210056]. CC received funding support form ANID Fondecyt [1240448]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
© The Author(s) 2024.