2004年，武汉大学生物技术专业，学士；
2009年，武汉大学微生物学专业，博士；
2010-2016年，伟德BETVlCTOR1946，博士后；
2016年至今，伟德BETVlCTOR1946，副教授。
B.S. 2004, Wuhan University, Biotechnology;
Ph.D. 2009, Wuhan University, Microbiology;
Postdoctoral Researcher, School of Life Sciences, Xiamen University, 2010-2016;
Associate professor, School of Life Sciences, Xiamen University, 2016-present.

我们实验室主要是利用基于DIA（Data-independent Acquisition, 数据不依赖型采集）定量质谱来研究细胞内信号通路。细胞中的信号传导大部分是由蛋白质复合物组装和解离来完成的。我们实验室利用定量质谱来研究细胞内源复合物的组装和解离，以期更深刻地理解信号细胞内信号传导过程。
我们首先利用亲和纯化（Affinity Purification）的方法纯化蛋白质复合物，然后利用DIA质谱技术鉴定和定量蛋白质复合物中的蛋白成分。我们称之为AP-DIA-MS方法。此套方法不仅可以鉴定参与信号通路中的未知蛋白，也可以研究蛋白复合物中已知蛋白成分的相对比例。此外，这个方法还可以研究复合物中翻译后修饰的动态变化，比如蛋白磷酸化在信号通路中作用。我们已经利用这套方法研究了TNF和LPS信号通路。未来我们会利用这个方法研究更多的信号通路。
Our lab focuses on the study of dynamic signaling pathway using DIA-MS based quantitative proteomics. Signal transduction in cells was generally mediated by dynamic assembly and dissociation of protein complexes. To gain an in-depth insight into the signaling transduction in cells, we employed quantitative mass spectrometry to investigate assembly and dissociation of endogenous protein complexes.
We fist purified protein complexes using affinity purification, and subsequently identified and quantified protein components of protein complexes using DIA-MS, which we referred to as AP-DIA workflow. The AP-DIA workflow can be utilized to identify novel proteins in the signaling pathway and investigate the stoichiometry of protein complexes. The AP-DIA workflow has been successfully employed to study the TNF and LPS signaling pathways.

代表性论文(^# co-first author, ^* Corresponding author):

1. Wen C, Wu X^*, Lin G, Yan W, Gan G, Xu X, Chen XY, Chen X, Liu X, Fu G^*, Zhong CQ^*. Evaluation of DDA Library-Free Strategies for Phosphoproteomics and Ubiquitinomics Data-Independent Acquisition Data. J Proteome Res. 2023 May 31 (IF=5.3)
2. Xu X, Yin F, Guo M, Gan G, Lin G, Wen C, Wang J, Song P, Wang J^*, Qi ZQ^*, Zhong CQ^*. Quantitative proteomic analysis of exosomes from umbilical cord mesenchymal stem cells and rat bone marrow stem cells. Proteomics. 2023 Jan. (IF=3.85)
3. Wen C, Gan G, Xu X, Lin G, Chen X, Wu Y, Xu Z, Wang J, Xie C, Wang HR^*, Zhong C. Q.^* Investigation of Effects of the Spectral Library on Analysis of diaPASEF Data. J Proteome Res. 2022 Feb 4;21(2):507-518. (IF=5.3)
4. Gan G., Xu X., Chen X., Zhang X.F., Wang J, Zhong C. Q.^* SCASP: a simple and robust sodium dodecyl sulfate-aided sample preparation method for proteomic research. Mol Cell Proteomics. 2021 Feb 4 (IF=7.2)
5. Li X^#, Zhong C. Q.^#, Wu R^#, Xu X, Yang ZH, Cai S, Wu X, Chen X, Yin Z, He Q, Li D, Xu F, Yan Y, Qi H, Xie C, Shuai J^*, Han J^*. RIP1-dependent linear and nonlinear recruitments of pro-caspase-8 and RIP3 respectively to necrosome specify distinct cell death outcomes. Protein Cell. 2021 Jan 2. (IF= 14.87)
6. Wang D, Gan G, Chen X, Zhong C.Q.^* QuantPipe: A User-Friendly Pipeline Software Tool for DIA Data Analysis Based on the OpenSWATH-PyProphet-TRIC Workflow. J Proteome Res. 2020 Oct 22. (IF=4.0)
7. Zhong C.Q.^#*, Wu J, Qiu X, Chen X, Xie C, Han J^*. Generation of a murine SWATH-MS spectral library to quantify more than 11,000 proteins. Scientific Data. 2020 Mar 26;7(1):104. (IF=5.929)
8. Zhong, C.Q.^#*, Wu R, Chen X, Wu S, Shuai J, Han J^*. Systematic Assessment of the Effect of Internal Library in Targeted Analysis of SWATH-MS. J Proteome Res. 2020 Jan 3;19(1):477-492. (IF=3.8)
9. Wu, X. ^#, Yang, D., Zhao, F., Yang Z.H., Wang, D., Qiao, M., Fang, Y., Li, W., Wu, R., He P., Cong, Y., Chen, C., Hu, L., Yan, Y., Xie, C., Wu, Y., Han, J. ^*, Zhong, C.Q.^* Quantification of dynamic protein interactions and phosphorylation in LPS signaling pathway by SWATH-MS. Mol Cell Proteomics. 2019 Jun;18(6):1054-1069 (IF=7.2)
10. Y. Li^#, C.Q. Zhong^#*, X. Xu, S. Cai, X. Wu, Y. Zhang, J. Chen, J. Shi, S. Lin, and J. Han^* (2015). Group-DIA: analyzing multiple data-independent acquisition mass spectrometry data files. Nature methods. 2015 Dec;12(12):1105-6 (IF=23.030)
11. W.T. He, H. Wan, L. Hu, P. Chen, X. Wang, Z. Huang, Z.H. Yang, C. Q. Zhong^*, J. Han^*. Gasdermin D is an executor of pyroptosis and required for interleukin-1β secretion. Cell Res. 2015 Dec;25(12):1285-98. (IF=15.393)
12. Zhong, C. Q.^#, Y. Li^#, D. Yang, N. Zhang, X. Xu, Y. Wu, J. Chen and J. Han^* (2014). Quantitative phosphoproteomic analysis of RIP3-dependent protein phosphorylation in the course of TNF-induced necroptosis. Proteomics 2014 Mar;14(6):713-24 (IF=3.060)
13. Wu, X. ^#, L. Tian^#, J. Li, Y. Zhang, V. Han, Y. Li, X. Xu, H. Li, X. Chen, J. Chen, W. Jin, Y. Xie, J. Han^* and C. Q. Zhong^*. Investigation of receptor interacting protein (RIP3)-dependent protein phosphorylation by quantitative phosphoproteomics. Mol Cell Proteomics 2012 Dec;11(12):1640-51. (IF=6.830)

荣誉、奖励及参加学术团体的情况: