CAS Key Laboratory of Soft Matter Chemistry, Department of Chemistry, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026, China.
Sci Rep. 2013;3:1848. doi: 10.1038/srep01848.
Herein, we report the rational design of a DEVD-based heptapeptide hydrogelator 1 which is susceptible to caspase-3 (CASP3), and its isomeric control hydrogelator 2 with a DEDV-based heptapeptide sequence. Self-assembly of 1 in water results in flexuous, long nanofibers to form supramolecular hydrogel I with higher mechanical strength than that of hydrogel II which is composed of rigid, short nanofibers of 2. In vitro enzymatic analysis indicated that 1 is susceptive to CASP3 while 2 is not. 3-(4,5-dimethylthiazol-2-yl) 2,5 diphenyl tetrazolium bromide (MTT) and Western blot analyses indicated that DEDV-based hydrogelator 2 induces cell death via apoptotic pathway while the DEVD-based hydrogelator 1 minimizes cellular apoptosis induction.
在这里,我们报告了一种基于 DEVD 的七肽水凝胶剂 1 的合理设计,该水凝胶剂 1 对 caspase-3(CASP3)敏感,以及与其具有 DEDV 基七肽序列的非对映异构体对照水凝胶剂 2。1 在水中自组装形成柔韧的长纳米纤维,形成具有比由刚性、短纳米纤维组成的水凝胶 II 更高机械强度的超分子水凝胶 I。体外酶分析表明,1 对 CASP3 敏感,而 2 则不敏感。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)和 Western blot 分析表明,DEDV 基水凝胶剂 2 通过凋亡途径诱导细胞死亡,而基于 DEVD 的水凝胶剂 1 则最大程度地减少细胞凋亡诱导。