Cell penetrating peptide (CPP) gold(iii) - complex - bioconjugates: from chemical design to interaction with cancer cells for nanomedicine applications.


Journal

Nanoscale advances
ISSN: 2516-0230
Titre abrégé: Nanoscale Adv
Pays: England
ID NLM: 101738708

Informations de publication

Date de publication:
15 Jul 2022
Historique:
received: 11 02 2022
accepted: 11 05 2022
entrez: 22 9 2022
pubmed: 23 9 2022
medline: 23 9 2022
Statut: epublish

Résumé

This study promotes an innovative synthesis of a nanotheragnostic scaffold capable of targeting and destroying pancreatic cancer cells (PDAC) using the Biotinylated NFL-TBS.40-63 peptide (BIOT-NFL), known to enter various glioblastoma cancer cells (GBM) where it specifically destroys their microtubule network. This recently proposed methodology (P7391FR00-50481 LIV) applied to other peptides VIM (Vimentin) and TAT (Twin-Arginine Translocation) (CPP peptides) has many advantages, such as targeted selective internalization and high stability under experimental conditions, modulated by steric and chemical configurations of peptides. The successful interaction of peptides on gold surfaces has been confirmed by UV-visible, dynamic light scattering (DLS), Zeta potential (ZP) and Raman spectroscopy analyses. The cellular internalization in pancreatic ductal adenocarcinoma (PDAC; MIA PACA-2) and GBM (F98) cells was monitored by transmission electron microscopy (TEM) and showed a better cellular internalization in the presence of peptides with gold nanoparticles. In this work, we also evaluated the power of these hybrid peptide-nanoparticles as photothermal agents after cancer cell internalization. These findings envisage novel perspectives for the development of high peptide-nanotheragnostics.

Identifiants

pubmed: 36133522
doi: 10.1039/d2na00096b
pii: d2na00096b
pmc: PMC9417459
doi:

Types de publication

Journal Article

Langues

eng

Pagination

3010-3022

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Celia Arib (C)

CNRS, UMR 7244, CSPBAT, Laboratoire de Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques Université Paris 13 Sorbonne Paris Cité Bobigny France jolanda.spadavecchia@univ-paris13.fr.

Audrey Griveau (A)

Laboratoire Micro et Nanomedecines Translationnelles, Inserm 1066, CNRS 6021, Institut de Recherche en Ingénierie de la Sante, Bâtiment IBS Institut de Biologie de la Sante, Université, Angers, Centre Hospitalier Universitaire Angers France.

Joel Eyer (J)

Laboratoire Micro et Nanomedecines Translationnelles, Inserm 1066, CNRS 6021, Institut de Recherche en Ingénierie de la Sante, Bâtiment IBS Institut de Biologie de la Sante, Université, Angers, Centre Hospitalier Universitaire Angers France.

Jolanda Spadavecchia (J)

CNRS, UMR 7244, CSPBAT, Laboratoire de Chimie, Structures et Propriétés de Biomatériaux et d'Agents Thérapeutiques Université Paris 13 Sorbonne Paris Cité Bobigny France jolanda.spadavecchia@univ-paris13.fr.

Classifications MeSH