Enzyme Catalysis in Non-Native Environment with Unnatural Selectivity Using Polymeric Nanoreactors

被引:15
|
作者
Gao, Jingjing [1 ,2 ,3 ,4 ]
Le, Stephanie [1 ]
Thayumanavan, S. [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[2] Brigham & Womens Hosp, Ctr Nanomed, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Anesthesiol, Div Engn Med, Boston, MA 02115 USA
[4] Harvard Med Sch, Boston, MA 02115 USA
关键词
amphiphilic copolymers; cross-linkers; polymeric nanoreactors; unnatural selectivity; DIRECTED EVOLUTION; CASCADE REACTIONS; PROTEINS; STABILIZATION; ENANTIOSELECTIVITY; NANOASSEMBLIES; PERMEABILITY; STABILITY; LIPASE;
D O I
10.1002/anie.202109477
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The utilization of enzymes for catalysis in organic solvents, while exhibiting selectivity to different substrates, is a big challenge. We report an amphiphilic random copolymer system that self-assembles with enzymes in an organic solvent to form nanoreactors. These encapsulated enzymes are not denatured and they do preserve the catalytic activity. The cross-linkable functional groups in the hydrophobic compartments of the polymers offer to control accessibility to the enzyme. This varied accessibility due to the polymer host, rather than the enzyme itself, endows the nanoreactor with an unnatural selectivity. The findings here highlight the significant potential of simple polymer-based enzyme nanoreactors to execute selective organic reactions under non-native conditions.
引用
收藏
页码:27189 / 27194
页数:6
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