Adenosine Triphosphate Templated Self-Assembly of Cationic Porphyrin into Chiral Double Superhelices and Enzyme-Mediated Disassembly

被引:64
|
作者
Li, Zhiliang [1 ,2 ]
Zeman, Charles J. [1 ,2 ]
Valandro, Silvano R. [1 ]
Bantang, Jose Paolo O. [1 ]
Schanze, Kirk S. [1 ]
机构
[1] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
关键词
SUPRAMOLECULAR POLYMERS; MOLECULAR-DYNAMICS; AMPLIFICATION;
D O I
10.1021/jacs.9b04133
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembly of small molecules through noncovalent interactions into nanoscale architectures has been extensively studied in supramolecular chemistry. However, it is still challenging to develop a biologically inspired self-assembly system that functions in water with complex structure and dynamics by analogy with those found in nature. Here, we report a new water-soluble cationic porphyrin that undergoes adenosine triphosphate (ATP)-templated self-assembly into right-handed double-helical supramolecular structures. Direct observation of the porphyrin-ATP assembly by transmission electron microscopy has been accomplished. The assemblies consist of superhelical fibers with length greater than 1 mu m and width similar to 46 nm. The chiral superhelical fibers show reversible disassembly to monomers upon hydrolysis of ATP catalyzed by alkaline phosphatase (ALP), and the nanofibers can be re-formed with subsequent addition of ATP. Moreover, transient self-assembly of a chiral double helix is formed when ALP is present to consume ATP.
引用
收藏
页码:12610 / 12618
页数:9
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