Computational Design of Novel Cyclic Peptides Endowed with Autophagy-Inhibiting Activity on Cancer Cell Lines.
Atg8
LC3B
LIR motif
autophagy inhibitors
cancer
peptide
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
24 Apr 2024
24 Apr 2024
Historique:
received:
26
03
2024
revised:
17
04
2024
accepted:
21
04
2024
medline:
11
5
2024
pubmed:
11
5
2024
entrez:
11
5
2024
Statut:
epublish
Résumé
(1) Autophagy plays a significant role in development and cell proliferation. This process is mainly accomplished by the LC3 protein, which, after maturation, builds the nascent autophagosomes. The inhibition of LC3 maturation results in the interference of autophagy activation. (2) In this study, starting from the structure of a known LC3B binder (LIR2-RavZ peptide), we identified new LC3B ligands by applying an in silico drug design strategy. The most promising peptides were synthesized, biophysically assayed, and biologically evaluated to ascertain their potential antiproliferative activity on five humans cell lines. (3) A cyclic peptide (named Pep6), endowed with high conformational stability (due to the presence of a disulfide bridge), displayed a K
Identifiants
pubmed: 38731842
pii: ijms25094622
doi: 10.3390/ijms25094622
pii:
doi:
Substances chimiques
Peptides, Cyclic
0
Antineoplastic Agents
0
Microtubule-Associated Proteins
0
MAP1LC3B protein, human
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM