潘孝敬
潘孝敬

特聘研究员

研究领域

结构生物学

个人邮箱

panxj@smart.org.cn

行政助理

沈晓华(shenxiaohua@smart.org.cn)

研究方向

主要运用结构生物学、生物化学及生理学等多学科手段,致力于探究重大疾病相关膜蛋白的工作机理与药物作用机制。当前重点关注与全身代谢性疾病、神经发育及调控相关的膜蛋白研究方向。

研究成果

潘孝敬,深圳医学科学院特聘研究员,国家自然科学基金优秀青年基金获得者。自博士后工作开始,先后获得中国博士后基金会的“博新计划”,国自然的青年基金,面上项目,北京市科委的“科技新星”等经费支持。潘孝敬在国际顶级学术期刊Science上以第一作者(含共一)发表文章5篇,以共通讯作者在PNASNature Communications等杂志发表文章9篇。

教育与工作经历

2023 - 至今深圳医学科学院 特聘研究员

2019 - 2023清华大学 生命科学院 副研究员

2016 - 2019清华大学 医学院 博士后

2011 - 2016清华大学 医学院 博士

2007 - 2011中国科学技术大学 生命科学院 学士

奖项荣誉

2021     中国博士后基金会优秀创新成果

2019     北京市科委评选“科技新星”

2019     清华大学结构生物学高精尖中心卓越青年科学家

2018     清华大学优秀博士后

2016     中国博士后基金会“博新计划”

2016     北京市优秀毕业生

2013     教育部博士生国家奖学金

2012     教育部硕士生国家奖学金

2012     教育部第十七届博士生学术新人奖

2012     清华大学“蒋南翔”奖学金

2011     安徽省优秀毕业生,中国科学技术大学优秀毕业生


代表论文

*代表共同第一作者,#代表共同通讯作者。


1.Huang, J., Pan, X.#,  Yan, N#. 2024. Structural biology and molecular pharmacology of voltage-gated ion channels. Nature Reviews Molecular Cell Biology, 1-22.


2.Shen, Z. *, Xu, L. *, Wu, T. *, Wang, H. *, Wang, Q., Ge, X., Huang, G., Pan, X.#. 2024. Structural basis for urate recognition and apigenin inhibition of human GLUT9. Nature Communications, 15(1), 5039.


3.Wu, Q.*, Huang, J.*#, Fan, X.*#, Wang, K.*, Jin, X., Huang, G., Li, J., Pan, X.# and Yan, N.#, 2023. Structural mapping of Nav1. 7 antagonists. Nature Communications, 14(1), p.3224.


4.Huang, G.*, Wu, Q.*, Li, Z.*, Jin, X.*, Huang, X., Wu, T., Pan, X.and Yan, N.#, 2022. Unwinding and spiral sliding of S4 and domain rotation of VSD during the electromechanical coupling in Nav1. 7. Proceedings of the National Academy of Sciences, 119(33), p.e2209164119.


5.Huang, X.*, Jin, X.*, Huang, G., Huang, J., Wu, T., Li, Z., Chen, J., Kong, F., Pan, X.and Yan, N.#, 2022. Structural basis for high-voltage activation and subtype-specific inhibition of human Nav1. 8. Proceedings of the National Academy of Sciences, 119(30), p.e2208211119.


6.Pan, X.*#, Li, Z.*, Jin, X.*, Zhao, Y.*, Huang, G.*, Huang, X., Shen, Z., Cao, Y., Dong, M., Lei, J. and Yan, N.#, 2021. Comparative structural analysis of human Nav1. 1 and Nav1. 5 reveals mutational hotspots for sodium channelopathies. Proceedings of the National Academy of Sciences, 118(11), p.e2100066118.


7.Li, Z., Jin, X., Wu, T., Zhao, X., Wang, W., Lei, J., Pan, X.and Yan, N.#, 2021. Structure of human Nav1. 5 reveals the fast inactivation-related segments as a mutational hotspot for the long QT syndrome. Proceedings of the National Academy of Sciences, 118(11), p.e2100069118.


8.Shen, H.#, Yan, N.and Pan, X.#, 2021. Structural determination of human Nav1. 4 and Nav1. 7 using single particle cryo-electron microscopy. Methods in Enzymology (Vol. 653, pp. 103-120). Academic Press.


9.Chi, X.*, Jin, X.*, Chen, Y.*, Lu, X., Tu, X., Li, X., Zhang, Y., Lei, J., Huang, J., Huang, Z.#, Zhou, Q.#, and Pan, X.#, 2020. Structural insights into the gating mechanism of human SLC26A9 mediated by its C-terminal sequence. Cell Discovery, 6(1), p.55.


10.Pan, X.*, Li, Z.*, Huang, X.*, Huang, G.*, Gao, S., Shen, H., Liu, L., Lei, J. and Yan, N., 2019. Molecular basis for pore blockade of human Na+ channel Nav1. 2 by the μ-conotoxin KIIIA. Science, 363(6433), pp.1309-1313.


11.Pan, X.*, Li, Z.*, Zhou, Q.*, Shen, H.*, Wu, K.*, Huang, X., Chen, J., Zhang, J., Zhu, X., Lei, J. and Xiong, W., Gong, H., Xiao, B., and Yan, N., 2018. Structure of the human voltage-gated sodium channel Nav1. 4 in complex with β1. Science.362(6412), p.eaau2486.


12.Shen, H.*, Li, Z.*, Jiang, Y.*, Pan, X.*, Wu, J., Cristofori-Armstrong, B., Smith, J.J., Chin, Y.K., Lei, J., Zhou, Q.#and King, G.F.#, and Yan, N.#, 2018. Structural basis for the modulation of voltage-gated sodium channels by animal toxins. Science, 362(6412), p.eaau2596.


13.Shen, H.*, Zhou, Q.*, Pan, X.*, Li, Z.*, Wu, J. and Yan, N., 2017. Structure of a eukaryotic voltage-gated sodium channel at near-atomic resolution. Science, 355(6328), p.eaal4326.


14.Deng, D.*, Yan, C.*, Pan, X.*, Mahfouz, M., Wang, J., Zhu, J.K., Shi, Y.#and Yan, N.#, 2012. Structural basis for sequence-specific recognition of DNA by TAL effectors. Science, 335(6069), pp.720-723.