A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule
A simple and unique bacterial fluorescence resonance energy transfer (FRET) platform is developed through metabolic biosynthetic pathways for the sensitive and ratiometric detection of innate immune defence molecule. Using this bacterial FRET platform, immune molecule lysozyme could be sensitively m...
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sg-ntu-dr.10356-1607742022-08-02T08:07:11Z A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule Zhang, Zhijun Han, Qinyu Lau, Junwei Wang, Zhimin Hu, Ming Qiu, Hao Thang, Do Cong Xing, Bengang School of Physical and Mathematical Sciences School of Chemical and Biomedical Engineering Science::Chemistry Lysozyme Bacterial Infection A simple and unique bacterial fluorescence resonance energy transfer (FRET) platform is developed through metabolic biosynthetic pathways for the sensitive and ratiometric detection of innate immune defence molecule. Using this bacterial FRET platform, immune molecule lysozyme could be sensitively monitored in buffer, in serum, and even in the secretion of infected immune cells. As an important defensive molecule of the innate immune system, lysozyme not only plays a significant role in mediating protection against microbial invasion, but also acts as a significant biomarker of leukemia, tuberculosis, meningitis and renal diseases. Considering the importance of perceiving lysozyme activity, this work sheds a light on the access of host's immune response of bacterial infection, as well as provides valuable guidance for the treatment of bacterial infection related diseases. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Z.Z. acknowledges the financial support from National Natural Science Foundation of China (NSFC) (No. 22007083), Zhejiang Provincial Natural Science Foundation of China (Grant No. LQ20B010010), and Science Foundation of Zhejiang Sci-Tech University (ZSTU) under Grant No. 19062410-Y. B.X. acknowledges the financial support from Tier 1 RG5/18 (S), RG6/20, MOE 2017-T2–2-110, Start-Up Grant (SUG), A*Star SERC A1983c0028 (M4070319), A20E5c0090, National Natural Science Foundation of China (NSFC) (No. 51929201). 2022-08-02T08:07:11Z 2022-08-02T08:07:11Z 2022 Journal Article Zhang, Z., Han, Q., Lau, J., Wang, Z., Hu, M., Qiu, H., Thang, D. C. & Xing, B. (2022). A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule. Sensors and Actuators B: Chemical, 350, 130913-. https://dx.doi.org/10.1016/j.snb.2021.130913 0925-4005 https://hdl.handle.net/10356/160774 10.1016/j.snb.2021.130913 2-s2.0-85117361455 350 130913 en RG5/18 (S) RG6/20 MOE 2017-T2–2-110 A1983c0028 (M4070319) A20E5c0090 Sensors and Actuators B: Chemical © 2021 Elsevier B.V. All rights reserved. |
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Science::Chemistry Lysozyme Bacterial Infection Zhang, Zhijun Han, Qinyu Lau, Junwei Wang, Zhimin Hu, Ming Qiu, Hao Thang, Do Cong Xing, Bengang A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
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A simple and unique bacterial fluorescence resonance energy transfer (FRET) platform is developed through metabolic biosynthetic pathways for the sensitive and ratiometric detection of innate immune defence molecule. Using this bacterial FRET platform, immune molecule lysozyme could be sensitively monitored in buffer, in serum, and even in the secretion of infected immune cells. As an important defensive molecule of the innate immune system, lysozyme not only plays a significant role in mediating protection against microbial invasion, but also acts as a significant biomarker of leukemia, tuberculosis, meningitis and renal diseases. Considering the importance of perceiving lysozyme activity, this work sheds a light on the access of host's immune response of bacterial infection, as well as provides valuable guidance for the treatment of bacterial infection related diseases. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Zhang, Zhijun Han, Qinyu Lau, Junwei Wang, Zhimin Hu, Ming Qiu, Hao Thang, Do Cong Xing, Bengang |
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Article |
author |
Zhang, Zhijun Han, Qinyu Lau, Junwei Wang, Zhimin Hu, Ming Qiu, Hao Thang, Do Cong Xing, Bengang |
author_sort |
Zhang, Zhijun |
title |
A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
title_short |
A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
title_full |
A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
title_fullStr |
A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
title_full_unstemmed |
A metabolic labeling way to in situ fabricate bacterial FRET platform for innate immune defence molecule |
title_sort |
metabolic labeling way to in situ fabricate bacterial fret platform for innate immune defence molecule |
publishDate |
2022 |
url |
https://hdl.handle.net/10356/160774 |
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1743119570001985536 |