Self-assembly of large and small molecules into hierarchically ordered sacs and membranes

被引:512
作者
Capito, Ramille M. [1 ]
Azevedo, Helena S. [1 ,2 ]
Velichko, Yuri S. [3 ]
Mata, Alvaro [1 ]
Stupp, Samuel I. [1 ,3 ,4 ,5 ]
机构
[1] Northwestern Univ, Inst Bionanotechnol Med, Chicago, IL 60611 USA
[2] Univ Minho, Dept Polymer Engn, 3Bs Res Grp, Braga, Portugal
[3] Northwestern Univ, Dept Mat Sci & Engn, Chicago, IL 60208 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[5] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
关键词
D O I
10.1126/science.1154586
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report here the self- assembly of macroscopic sacs and membranes at the interface between two aqueous solutions, one containing a megadalton polymer and the other, small self- assembling molecules bearing opposite charge. The resulting structures have a highly ordered architecture in which nanofiber bundles align and reorient by nearly 90 degrees as the membrane grows. The formation of a diffusion barrier upon contact between the two liquids prevents their chaotic mixing. We hypothesize that growth of the membrane is then driven by a dynamic synergy between osmotic pressure of ions and static self- assembly. These robust, self- sealing macroscopic structures offer opportunities in many areas, including the formation of privileged environments for cells, immune barriers, new biological assays, and self- assembly of ordered thick membranes for diverse applications.
引用
收藏
页码:1812 / 1816
页数:5
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