α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition

Cell delivery of therapeutic macromolecules and nanoparticles is a critical drug development challenge. Translocation through lipid raft-mediated endocytic mechanisms is being sought, as it can avoid rapid lysosomal degradation. Here, we present a set of short α/β-peptide tags with high affinity to...

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Main Authors: Anasztázia Hetényi, Enikő Szabó, Norbert Imre, Kaushik Nath Bhaumik, Attila Tököli, Tamás Füzesi, Réka Hollandi, Peter Horvath, Ágnes Czibula, Éva Monostori, Mária A. Deli, Tamás A. Martinek
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/3/580
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author Anasztázia Hetényi
Enikő Szabó
Norbert Imre
Kaushik Nath Bhaumik
Attila Tököli
Tamás Füzesi
Réka Hollandi
Peter Horvath
Ágnes Czibula
Éva Monostori
Mária A. Deli
Tamás A. Martinek
author_facet Anasztázia Hetényi
Enikő Szabó
Norbert Imre
Kaushik Nath Bhaumik
Attila Tököli
Tamás Füzesi
Réka Hollandi
Peter Horvath
Ágnes Czibula
Éva Monostori
Mária A. Deli
Tamás A. Martinek
author_sort Anasztázia Hetényi
collection DOAJ
description Cell delivery of therapeutic macromolecules and nanoparticles is a critical drug development challenge. Translocation through lipid raft-mediated endocytic mechanisms is being sought, as it can avoid rapid lysosomal degradation. Here, we present a set of short α/β-peptide tags with high affinity to the lipid raft-associated ganglioside GM1. These sequences induce effective internalization of the attached immunoglobulin cargo. The structural requirements of the GM1-peptide interaction are presented, and the importance of the membrane components are shown. The results contribute to the development of a receptor-based cell delivery platform.
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spelling doaj.art-b7ffb04ba3d847a5a22677125d34c90c2023-11-30T21:56:56ZengMDPI AGPharmaceutics1999-49232022-03-0114358010.3390/pharmaceutics14030580α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside RecognitionAnasztázia Hetényi0Enikő Szabó1Norbert Imre2Kaushik Nath Bhaumik3Attila Tököli4Tamás Füzesi5Réka Hollandi6Peter Horvath7Ágnes Czibula8Éva Monostori9Mária A. Deli10Tamás A. Martinek11Department of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryInstitute of Genetics, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryInstitute of Biophysics, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryInstitute of Biophysics, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryInstitute of Genetics, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryInstitute of Genetics, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungarySynthetic and Systems Biology Unit, Biological Research Centre, Temesvári krt. 62, 6726 Szeged, HungaryDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, 6720 Szeged, HungaryCell delivery of therapeutic macromolecules and nanoparticles is a critical drug development challenge. Translocation through lipid raft-mediated endocytic mechanisms is being sought, as it can avoid rapid lysosomal degradation. Here, we present a set of short α/β-peptide tags with high affinity to the lipid raft-associated ganglioside GM1. These sequences induce effective internalization of the attached immunoglobulin cargo. The structural requirements of the GM1-peptide interaction are presented, and the importance of the membrane components are shown. The results contribute to the development of a receptor-based cell delivery platform.https://www.mdpi.com/1999-4923/14/3/580cell deliveryglycan recognitionalpha-beta peptideendocytosisimmunoglobulin
spellingShingle Anasztázia Hetényi
Enikő Szabó
Norbert Imre
Kaushik Nath Bhaumik
Attila Tököli
Tamás Füzesi
Réka Hollandi
Peter Horvath
Ágnes Czibula
Éva Monostori
Mária A. Deli
Tamás A. Martinek
α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
Pharmaceutics
cell delivery
glycan recognition
alpha-beta peptide
endocytosis
immunoglobulin
title α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
title_full α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
title_fullStr α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
title_full_unstemmed α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
title_short α/β-Peptides as Nanomolar Triggers of Lipid Raft-Mediated Endocytosis through GM1 Ganglioside Recognition
title_sort α β peptides as nanomolar triggers of lipid raft mediated endocytosis through gm1 ganglioside recognition
topic cell delivery
glycan recognition
alpha-beta peptide
endocytosis
immunoglobulin
url https://www.mdpi.com/1999-4923/14/3/580
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