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A Second Life for MAP, a Model Amphipathic Peptide

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2022 Aug 12
PMID 35955457
Authors
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Abstract

Cell-penetrating peptides (CPP) have been shown to be efficient in the transport of cargoes into the cells, namely siRNA and DNA, proteins and peptides, and in some cases, small therapeutics. These peptides have emerged as a solution to increase drug concentrations in different tissues and various cell types, therefore having a relevant therapeutic relevance which led to clinical trials. One of them, MAP, is a model amphipathic peptide with an α-helical conformation and both hydrophilic and hydrophobic residues in opposite sides of the helix. It is composed of a mixture of alanines, leucines, and lysines (KLALKLALKALKAALKLA). The CPP MAP has the ability to translocate oligonucleotides, peptides and small proteins. However, taking advantage of its unique properties, in recent years innovative concepts were developed, such as in silico studies of modelling with receptors, coupling and repurposing drugs in the central nervous system and oncology, or involving the construction of dual-drug delivery systems using nanoparticles. In addition to designs of MAP-linked vehicles and strategies to achieve highly effective yet less toxic chemotherapy, this review will be focused on unique molecular structure and how it determines its cellular activity, and also intends to address the most recent and frankly motivating issues for the future.

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References
1.
Borrelli A, Tornesello A, Tornesello M, Buonaguro F . Cell Penetrating Peptides as Molecular Carriers for Anti-Cancer Agents. Molecules. 2018; 23(2). PMC: 6017757. DOI: 10.3390/molecules23020295. View

2.
Wada S, Hashimoto Y, Kawai Y, Miyata K, Tsuda H, Nakagawa O . Effect of Ala replacement with Aib in amphipathic cell-penetrating peptide on oligonucleotide delivery into cells. Bioorg Med Chem. 2013; 21(24):7669-73. DOI: 10.1016/j.bmc.2013.10.029. View

3.
Pierige F, Serafini S, Rossi L, Magnani M . Cell-based drug delivery. Adv Drug Deliv Rev. 2007; 60(2):286-95. DOI: 10.1016/j.addr.2007.08.029. View

4.
Janek K, Rothemund S, Gast K, Beyermann M, Zipper J, Fabian H . Study of the conformational transition of A beta(1-42) using D-amino acid replacement analogues. Biochemistry. 2001; 40(18):5457-63. DOI: 10.1021/bi002005e. View

5.
Bocsik A, Walter F, Gyebrovszki A, Fulop L, Blasig I, Dabrowski S . Reversible Opening of Intercellular Junctions of Intestinal Epithelial and Brain Endothelial Cells With Tight Junction Modulator Peptides. J Pharm Sci. 2016; 105(2):754-765. DOI: 10.1016/j.xphs.2015.11.018. View