TY - JOUR
T1 - Protein-Structure-Directed Metal–Organic Zeolite-like Networks as Biomacromolecule Carriers
AU - Wang, Huanrong
AU - Han, Lin
AU - Zheng, Dong
AU - Yang, Mingfang
AU - Andaloussi, Yassin H.
AU - Cheng, Peng
AU - Zhang, Zhenjie
AU - Ma, Shengqian
AU - Zaworotko, Michael J.
AU - Feng, Yifan
AU - Chen, Yao
N1 - Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/4/6
Y1 - 2020/4/6
N2 - Fabrication of zeolite-like metal–organic frameworks (ZMOFs) for advanced applications, such as enzyme immobilization, is of great interest but is a great synthetic challenge. Herein, we have developed a new strategy using proteins as structure-directed agents to direct the formation of new ZMOFs that can act as versatile platforms for the in situ encapsulation of proteins under ambient conditions. Notably, protein incorporation directs the formation of a ZMOF with a sodalite (sod) topology instead of a non-porous diamondoid (dia) topology under analogous synthetic conditions. Histidines in proteins play a crucial role in the observed templating effect. Modulating histidine content thereby influenced the resultant MOF product (from dia to dia + sod mixture and, ultimately, to sod MOF). Moreover, the resulting ZMOF-incorporated proteins preserved their activity even after exposure to high temperatures and organic solvents, demonstrating their potential for biocatalysis and biopharmaceutical applications.
AB - Fabrication of zeolite-like metal–organic frameworks (ZMOFs) for advanced applications, such as enzyme immobilization, is of great interest but is a great synthetic challenge. Herein, we have developed a new strategy using proteins as structure-directed agents to direct the formation of new ZMOFs that can act as versatile platforms for the in situ encapsulation of proteins under ambient conditions. Notably, protein incorporation directs the formation of a ZMOF with a sodalite (sod) topology instead of a non-porous diamondoid (dia) topology under analogous synthetic conditions. Histidines in proteins play a crucial role in the observed templating effect. Modulating histidine content thereby influenced the resultant MOF product (from dia to dia + sod mixture and, ultimately, to sod MOF). Moreover, the resulting ZMOF-incorporated proteins preserved their activity even after exposure to high temperatures and organic solvents, demonstrating their potential for biocatalysis and biopharmaceutical applications.
KW - enzyme immobilization
KW - metal–organic frameworks
KW - protein structure
KW - self-assembly
KW - template synthesis
KW - zeolite analogues
UR - http://www.scopus.com/inward/record.url?scp=85080976121&partnerID=8YFLogxK
U2 - 10.1002/anie.202000299
DO - 10.1002/anie.202000299
M3 - Article
C2 - 32011779
AN - SCOPUS:85080976121
SN - 1433-7851
VL - 59
SP - 6263
EP - 6267
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 15
ER -