Enzyme Encapsulation in a Porous Hydrogen-Bonded Organic Framework

被引:273
作者
Liang, Weibin [1 ,2 ]
Carraro, Francesco [3 ]
Solomon, Marcello B. [3 ]
Bell, Stephen G. [1 ,2 ]
Amenitsch, Heinz [4 ]
Sumby, Christopher J. [1 ,2 ]
White, Nicholas G. [5 ]
Falcaro, Paolo [1 ,2 ,3 ]
Doonan, Christian J. [1 ,2 ]
机构
[1] Univ Adelaide, Dept Chem, Adelaide, SA 5005, Australia
[2] Univ Adelaide, Ctr Adv Nanomat, Adelaide, SA 5005, Australia
[3] Graz Univ Technol, Inst Phys & Theoret Chem, Stremayrgasse 9, A-8010 Graz, Austria
[4] Graz Univ Technol, Inst Inorgan Chem, Stremayrgasse 9, A-8010 Graz, Austria
[5] Australian Natl Univ, Res Sch Chem, Canberra, ACT 2600, Australia
基金
澳大利亚研究理事会;
关键词
EMBEDDING ENZYMES; ALCOHOL OXIDASE; SCATTERING; PERFORMANCE; NETWORKS; PROTEINS; BEAMLINE; CATALASE;
D O I
10.1021/jacs.9b06589
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Protection of biological assemblies is critical to applications in biotechnology, increasing the durability of enzymes in biocatalysis or potentially stabilizing biotherapeutics during transport and use. Here we show that a porous hydrogen-bonded organic framework (HOF) constructed from water-soluble tetra-amidinium (1-Cl-4) and tetracarboxylate (2) building blocks can encapsulate and stabilize biomolecules to elevated temperature, proteolytic and denaturing agents, and extend the operable pH range for catalase activity. The HOF, which readily retains water within its framework structure, can also protect and retain the activity of enzymes such as alcohol oxidase, that are inactive when encapsulated within zeolitic imidazolate framework (ZIF) materials. Such HOF coatings could provide valid alternative materials to ZIFs: they are metal free, possess larger pore apertures, and are stable over a wider, more biologically relevant pH range.
引用
收藏
页码:14298 / 14305
页数:8
相关论文
共 59 条
[1]   First performance assessment of the small-angle X-ray scattering beamline at ELETTRA [J].
Amenitsch, H ;
Rappolt, M ;
Kriechbaum, M ;
Mio, H ;
Laggner, P ;
Bernstorff, S .
JOURNAL OF SYNCHROTRON RADIATION, 1998, 5 :506-508
[2]   THEORY OF DYNAMIC LIGHT-SCATTERING FROM POLYDISPERSE SYSTEMS [J].
ARAGON, SR ;
PECORA, R .
JOURNAL OF CHEMICAL PHYSICS, 1976, 64 (06) :2395-2404
[3]   The molecular basis for the chemical denaturation of proteins by urea [J].
Bennion, BJ ;
Daggett, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5142-5147
[4]   Molecular Tectonics: A Node-and-Linker Building Block Approach to a Family of Hydrogen-Bonded Frameworks [J].
Boer, Stephanie A. ;
Morshedi, Mahbod ;
Tarzia, Andrew ;
Doonan, Christian J. ;
White, Nicholas G. .
CHEMISTRY-A EUROPEAN JOURNAL, 2019, 25 (42) :10006-10012
[5]   Stabilizing biocatalysts [J].
Bommarius, Andreas S. ;
Paye, Marietou F. .
CHEMICAL SOCIETY REVIEWS, 2013, 42 (15) :6534-6565
[6]  
CHANCE B, 1952, J BIOL CHEM, V194, P471
[7]   Biocatalytic cascades driven by enzymes encapsulated in metal-organic framework nanoparticles [J].
Chen, Wei-Hai ;
Vazquez-Gonzalez, Margarita ;
Zoabi, Amani ;
Abu-Reziq, Raed ;
Willner, Itamar .
NATURE CATALYSIS, 2018, 1 (09) :689-695
[8]   Error bars in experimental biology [J].
Cumming, Geoff ;
Fidler, Fiona ;
Vaux, David L. .
JOURNAL OF CELL BIOLOGY, 2007, 177 (01) :7-11
[9]   Ultraviolet-Visible (UV-Vis) and Fluorescence Spectroscopic Investigation of the Interactions of Ionic Liquids and Catalase [J].
Dong, Xing ;
Fan, Yunchang ;
Yang, Peng ;
Kong, Jichuan ;
Li, Dandan ;
Miao, Juan ;
Hua, Shaofeng ;
Hu, Chaobing .
APPLIED SPECTROSCOPY, 2016, 70 (11) :1851-1860
[10]   Metal-Organic Frameworks at the Biointerface: Synthetic Strategies and Applications [J].
Doonan, Christian ;
Ricco, Raffaele ;
Liang, Kang ;
Bradshaw, Darren ;
Falcaro, Paolo .
ACCOUNTS OF CHEMICAL RESEARCH, 2017, 50 (06) :1423-1432