| Literature DB >> 33051947 |
Yu-Chen Pan1, Andrea Barba-Bon2, Han-Wen Tian1, Fei Ding1, Andreas Hennig2,3,4, Werner M Nau2, Dong-Sheng Guo1.
Abstract
Lysine (K) is an important target residue for protein and peptide delivery across membranes. K is the most frequently exposed residue in proteins, leading to high demand for the development of K-compatible transport activators. However, designing activators for K-rich peptides and proteins is more challenging than for arginine-rich species because of the kosmotropic nature of K and its recognition difficulty. In this study, we designed a new amphiphilic sulfonatocalix[5]arene (sCx5-6C) as a K-compatible transport activator. sCx5-6C was tailored with two key elements, recognition of K and the ability to embed into membranes. We measured the membrane transport efficiencies of α-poly-l-lysine, heptalysine, and histones across artificial membranes and of α-poly-l-lysine into live cells, activated by sCx5-6C. The results demonstrate that sCx5-6C acts as an efficient activator for translocating K-rich peptides and proteins, which cannot be achieved by known arginine-compatible activators.Entities:
Keywords: activators; calixarenes; lysine; membrane transport; molecular recognition
Year: 2020 PMID: 33051947 DOI: 10.1002/anie.202011185
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336