相关链接
联系方式
  • 通信地址:长春市前进大街2699号吉林大学超分子楼
  • 邮编:130012
  • 电话:0431-85168491
  • 传真:
  • Email:
当前位置:> 首页 > 论文著作 > 正文
ACS Nano--Self-Assembly of Cricoid Proteins Induced by “Soft Nanoparticles”: An Approach To Design Multienzyme-Cooperative Antioxidative Systems
作者:Sun, Hongcheng; Miao, Lu; Li, Jiaxi; et al.
关键字:Self-Assembly,Proteins
论文来源:期刊
具体来源:ACS Nano
发表时间:2015年
A strategy to construct high-ordered protein nanowires by electrostatic assembly of cricoid proteins and “soft nanoparticles” was developed. Poly(amido amine) (PAMAM) dendrimers on high generation that have been shown to be near-globular macromolecules with all of the amino groups distributing throughout the surface were ideal electropositive “soft nanoparticles” to induce electrostatic assembly of electronegative cricoid proteins. Atomic force microscopy and transmission electron microscopy all showed that one “soft nanoparticle” (generation 5 PAMAM, PD5) could electrostatically interact with two cricoid proteins (stable protein one, SP1) in an opposite orientation to form sandwich structure, further leading to self-assembled protein nanowires. The designed nanostructures could act as versatile scaffolds to develop multienzyme-cooperative antioxidative systems. By means of inducing catalytic selenocysteine and manganese porphyrin to SP1 and PD5, respectively, we successfully designed antioxidative protein nanowires with both excellent glutathione peroxidase and superoxide dismutase activities. Also, the introduction of selenocysteine and manganese porphyrin did not affect the assembly morphologies. Moreover, this multienzyme-cooperative antioxidative system exhibited excellent biological effect and low cell cytotoxicity.