| Literature DB >> 28948715 |
Govind S Bhosle1,2, Moneesha Fernandes1,2.
Abstract
Arginine-rich peptides having the (R-X-R)n motif are among the most effective cell-penetrating peptides (CPPs). Herein we report a several-fold increase in the efficacy of such CPPs if the linear flexible spacer (-X-) in the (R-X-R) motif is replaced by constrained cyclic 1,4-substituted-cyclohexane-derived spacers. Internalization of these oligomers in mammalian cell lines was found to be an energy-dependent process. Incorporation of these constrained, non-proteinogenic amino acid spacers in the CPPs is shown to enhance their proteolytic stability.Entities:
Keywords: (R-X-R)-motif; cell-penetrating peptides; cellular uptake; protease stability
Mesh:
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Year: 2017 PMID: 28948715 DOI: 10.1002/cmdc.201700498
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466