当前位置:
X-MOL 学术
›
J. Am. Chem. Soc.
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Galloyl Dialkyl Lipids Drive Encapsulation of Peptides into Lipid Nanoparticles by Hydrogen Bonding
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-12-19 , DOI: 10.1021/jacs.4c15688 Tingting Ye, Yong Chen, Zifu Zhong, Yi Huang, Jamie De Baere, Mark Gontsarik, Kim Deswarte, Bianka Golba, Martijn Risseeuw, Serge Van Calenbergh, Bart N. Lambrecht, Bruno G. De Geest
Journal of the American Chemical Society ( IF 14.4 ) Pub Date : 2024-12-19 , DOI: 10.1021/jacs.4c15688 Tingting Ye, Yong Chen, Zifu Zhong, Yi Huang, Jamie De Baere, Mark Gontsarik, Kim Deswarte, Bianka Golba, Martijn Risseeuw, Serge Van Calenbergh, Bart N. Lambrecht, Bruno G. De Geest
The intracellular delivery of peptides and proteins is crucial for various biomedical applications. Lipid nanoparticles (LNPs) have emerged as a promising strategy for delivering peptides to phagocytic cells. However, the diverse physicochemical properties of peptides necessitate tailored formulations. This study introduces a generic approach using galloyl (GA)-functionalized lipids for the encapsulation of peptides in LNPs via hydrogen bonding between the ubiquitously present amides in peptides and the multivalently displayed galloyl phenol groups in GA-LNPs. In vitro studies showed that GA-LNPs significantly improved the cellular uptake of peptides and activated immune responses when combined with Toll-like receptor (TLR) agonists MPLA and IMDQ. In vivo, GA-LNPs accumulated in the spleen and enhanced peptide delivery to antigen-presenting cells. GA-LNPs coencapsulating peptide antigens and TLR agonists elicited robust antigen-specific CD8+ T-cell responses in mice.
更新日期:2024-12-20