Yanbin Jiang

Prof. Dr. Yanbin Jiang

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 June 2020 in Frontiers in Bioengineering and Biotechnology
Verified
Journal Article
Open access
PDF file
HXHuan Xia
Huan Xia
NLNa Li
Na Li
XZXue Zhong
Xue Zhong
YJYanbin Jiang
Yanbin Jiang
Enzymes, as natural catalysts with remarkable catalytic activity and high region-selectivities, hold great promise in industrial catalysis. However, applications of enzymatic transformation are hampered by the fragility of enzymes in harsh conditions. Recently, metal–organic frameworks (MOFs), due to their high stability and available structural properties, have emerged as a promising platform for enzyme immobilization. Synthetic strategies of enzyme-MOF composites mainly including surface immobilization, covalent linkage, pore entrapment and in situ synthesis. Compared with free enzymes, most immobilized enzymes exhibit enhanced resistance against solvents and high temperatures. Besides, MOFs serving as matrixes for enzyme immobilization show extraordinary superiority in many aspects compared with other supporting materials. The advantages of using MOFs to support enzymes are discussed. To obtain a high enzyme loading capacity and to reduce the diffusion resistance of reactants and products during the reaction, the mesoporous MOFs have been designed and constructed. This review also covers the applications of enzyme-MOF composites in bio-sensing and detection, bio-catalysis, and cancer therapy, which is concerned with interdisciplinary nano-chemistry, material science and medical chemistry. Finally, some perspectives on reservation or enhancement of bio-catalytic activity of enzyme-MOF composites and the future of enzyme immobilization strategies are discussed.

1 February 2020 in Chemical Engineering Journal
Verified
Journal Article
Closed access
XZXue Zhong
Xue Zhong
HXHuan Xia
Huan Xia
WHWenquan Huang
Wenquan Huang
ZLZhixian Li
Zhixian Li
YJYanbin Jiang
Yanbin Jiang

1 October 2017 in Acta Biomaterialia
Verified
Journal Article
Closed access
HWHongdi Wang
Hongdi Wang
WZWei Zhu
Wei Zhu
YHYunna Huang
Yunna Huang
ZLZhixian Li
Zhixian Li
YJYanbin Jiang
Yanbin Jiang
QXQiuling Xie
Qiuling Xie

19 October 2024 in ACS Catalysis
Verified
Journal Article
Closed access
XTXiaolong Tang
Xiaolong Tang
CYChanglin Yu
Changlin Yu
JZJiaming Zhang
Jiaming Zhang
KLKaiwei Liu
Kaiwei Liu
DZDebin Zeng
Debin Zeng
Yongfa ZhuYongfa Zhu
Yongfa Zhu

1 January 2018 in Journal of Cereal Science
Verified
Journal Article
Closed access
WHWeizhi Huo
Weizhi Huo
DWDongwei Wei
Dongwei Wei
WZWei Zhu
Wei Zhu
ZLZhixian Li
Zhixian Li
YJYanbin Jiang
Yanbin Jiang

20 September 2017 in Nanoscale
Verified
Journal Article
Closed access
PDF file
ZLZhixian Li
Zhixian Li
HXHuan Xia
Huan Xia
SLShaomin Li
Shaomin Li
JPJiafeng Pang
Jiafeng Pang
WZWei Zhu
Wei Zhu
YJYanbin Jiang
Yanbin Jiang
By incorporating Cytochrome c (peroxidase, Cyt c) into a skeleton of its corresponding synthetic MOF analogue (peroxidase mimic, CuBDC), approximately 12-fold catalytic efficiency (kcat/KM) enhancement is observed compared to free Cyt c. Meanwhile, the shield endowed by CuBDC prevents encapsulated enzymes from deactivation by trypsin digestion, thermal treatment and long-term storage in vitro. This concept of combining enzymes and their MOF mimics with enhanced enzymatic activity and stability may provide new insights into the design of highly active, stable enzyme–MOF composite catalysts and holds promise for applications in biocatalysis, biosensing and drug delivery systems.