Modulating the biofunctionality of enzyme-MOF nanobiocatalyst through structure-switching aptamer for continuous degradation of BPA

适体 化学 降级(电信) 材料科学 生物物理学 生物化学 计算机科学 分子生物学 生物 电信
作者
Yuanyuan Liu,Yihan Liu,Linyan Gu,Juan Han,Wenjing Zhi,Yun Wang,Lei Wang
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:208: 112099-112099 被引量:7
标识
DOI:10.1016/j.colsurfb.2021.112099
摘要

• Biofunctionality was regulated automatically through structure-switching aptamer. • HRP-ZIF-8@P1 relied on substrate self-enriching to boost the activity. • HRP-ZIF-8@P1 could be completely recovered by magnetically controllable cDNA. • The cyclic catalysis automatically start based on competitive release. • The enhanced stability was provided by dual-layer protection of ZIF-8 and P1. Encapsulating enzyme within MOF (enzyme-MOF) gives rise to new opportunity to improve the fragility of enzyme, but practical application of enzyme-MOF composite is far from being realized. The development of a novel enzyme-MOF composite system should simultaneously guarantee the enhanced activity and controllably complete recycling, and only in this way can we efficiently and economically utilize the enzyme-MOF composite. Herein, we addressed all these fundamental limitations of current enzyme-MOF composite by establishing aptamer-functionalized enzyme-MOF composite (HRP-ZIF-8@P1). HRP-ZIF-8@P1 relied on automatic structure switch of aptamer-target binding and aptamer-cDNA (complementary DNA) hybridization, achieving effectiveness in self-enriching substrate around HRP-ZIF-8@P1 to boost enzymatic activity first, subsequently hybridizing spontaneously with magnetically controllable cDNA sequence (Fe 3 O 4 @P3) to completely recover the HRP-ZIF-8@P1, where preferentially capturing substrate could further induce the release of the hybridized HRP-ZIF-8@P1 for automatically starting the cyclic enzyme catalysis. A 5.6-fold enhancement in the catalytic efficiency for BPA degradation was endowed, and 94.7% catalytic activity was retained for 8 consecutive degradations of BPA, both of which were even more significant than HRP-ZIF-8. Additionally, remarkable stability of HRP-ZIF-8@P1 was afforded by dual-layer protection of ZIF-8 and P1 in denaturing conditions. Taking the possibility of discovering an aptamer for any target into account, the aptamer-functionalized enzyme-MOF composites provide a generic and simple guide for simultaneously boosting enzymatic activity and controllably full recycling the enzyme-MOF systems, accelerating their commercial utilizations.
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