Tang Haizhong, Doerksen Robert J, Jones Ticora V, Klein Michael L, Tew Gregory N
Polymer Science and Engineering Department, University of Massachusetts, 120 Governors Drive, Amherst, Massachusetts 01003, USA.
Chem Biol. 2006 Apr;13(4):427-35. doi: 10.1016/j.chembiol.2006.02.007.
A foldamer has been designed with a conformationally stiff backbone that is facially amphiphilic. The oligomer has excellent antimicrobial activity and was found to be 18 times more active toward bacterial cells than human red blood cells. The oligomer is built from arylamide bonds around a central 4,6-dicarboxy pyrimidine ring. The conformation was studied by X-ray crystallography and solution NMR spectroscopy. Density-functional (DFT) calculations were performed to guide the design. These calculations accurately predicted the overall conformation as well as NMR chemical shifts. Antibacterial activity was demonstrated against E. coli, a gram-negative strain, and B. subtilis, a gram-positive strain. The minimal inhibitory concentration is 0.8 microg/ml.
一种折叠体已被设计出来,其具有构象刚性的主链且具有表面两亲性。该低聚物具有出色的抗菌活性,并且发现其对细菌细胞的活性比对人类红细胞高18倍。该低聚物由围绕中心4,6-二羧基嘧啶环的芳基酰胺键构建而成。通过X射线晶体学和溶液核磁共振光谱研究了其构象。进行了密度泛函(DFT)计算以指导设计。这些计算准确地预测了整体构象以及核磁共振化学位移。对革兰氏阴性菌株大肠杆菌和革兰氏阳性菌株枯草芽孢杆菌均表现出抗菌活性。最低抑菌浓度为0.8微克/毫升。