学历: 博士研究生
邮箱: Zhenyi.Hu@sioc.ac.cn
电话:
地址: 上海市浦东新区海科路100号13号楼邮编:201210
2005 – 2009 药物制剂 中国药科大学,学士
2009 – 2012 药物化学 中国科学院上海药物研究所,硕士(导师:叶阳 教授)
2012 – 2013 药物化学生物学 清华大学,科研助理(导师:廖学斌 教授)
2013 – 2018 药物化学生物学 科罗拉多大学博尔德分校,博士(导师:尹航 教授)
2018 – 2023 药物化学生物学 耶鲁大学,博士后(导师:Craig Crews 教授)
2023.5 - 至今 药物化学生物学 中国科学院生物与化学交叉研究中心,研究员、课题组长
胡振一研究员博士毕业于科罗拉多大学博尔德分校,师从尹航教授;博后师从PROTAC技术的创始人-耶鲁大学的Craig Crews教授(合作导师 Yansheng Liu教授)。胡振一研究员聚焦于药物化学生物学,以自身免疫疾病与癌症为目标,在重要蛋白的小分子抑制剂研发方面积累了丰富的经验:首次通过基于结构的理性设计等方法研发了高效TLR8小分子抑制剂,TLR8抑制剂获得国际、美国和中国专利并转让,已获得中国和美国FDA临床受理,启动了临床试验;首次研发了继PROTAC之后的新一代靶向蛋白磷酸化的双功能小分子抑制剂(PhosTAC),其相较传统激酶抑制剂具有高效精确特异性等优点,PhosTAC作为新的通用型药物开发平台型技术,有广泛应用潜力。胡振一研究员以第一/共一/共同通讯作者在Nature Chemical Biology,Journal of the American Chemical Society,Cell Chemical Biology,ACS Chemical Biology等专业期刊上发表论文7篇,以上工作获得国际同行的高度认可,多次被C&EN、Science Trends、Trends in Pharmacological Sciences 和 Science Daily等期刊和科学媒体报道。
致力于利用化学手段研究和调控生命活动过程。本课题组聚焦于双功能分子(PROTAC,PhosTAC等),以生物功能为目标,以化学合成为手段 (Biology driven,chemistry empowered),调控生命和疾病的发生过程,做生命的工程师。我们的目标是基于双功能分子药物,开发老年痴呆症、癌症等疾病的治疗方法。
1. Hu,Z.#;Chen,P.#;Li,W.;Douglas,T.;Hines,J.;Liu,Y.;Crews,C.;Targeted Dephosphorylation of Tau by Phosphorylation Targeting Chimeras (PhosTACs) as a Therapeutic Modality. Journal of the American Chemical Society. 2023,145,7,4045–4055
2. Zhang,S.#; Hu,Z.#;Tanji,H.;Jiang,S.;Das,N.;Li,J.;Sakaniwa,K.;Jin,J.;Bian,Y.;Ohto,U.;Shimizu,T.;Yin,H.;Inhibition of Toll-like Receptor 8 through stabilization of its resting state. Nature Chemical Biology. 2018,14,58-64 (cover article)
3. Hu,Z.;Tanji,H.;Koo,K.;Chan,J.;Zhang,S.;Candia,A.;Shimizu,T.;Yin,H.;Small-molecule TLR8 antagonists via structure-based rational design. Cell Chemical Biology. 2018,25,1286–1291 (cover article)
4. Hu,Z.;Crews,C.;Recent Developments in PROTAC-Mediated Protein Degradation: From Bench to Clinic. Chembiochem. 2022,23 (2),e202100270.
5. Chen,P. #; Hu,Z. #;An,E.;Okeke,I.;Zheng,S.;Lo,X.;Gong,A.;Jaime-Figueroa,S.;Crews,C.;Modulation of Phosphoprotein Activity by Phosphorylation Targeting Chimeras (PhosTACs). ACS Chemical Biology. 2021,16,12,2808–2815.
6. Hu,Z.;Zhang,T.;Jiang,S.;Yin,H.;Protocol for evaluation and validation of TLR8 antagonists in HEK-Blue cells via secreted embryonic alkaline phosphatase assay. Cell Star Protocols. 2022,3,101061.
7. Samarasinghe,K.;Jaime-Figueroa,S.;Burgess,M.;Nalawansha,D.;Dai,K.; Hu,Z.;Bebenek,A.;Holley,S.;Crews,C.;Targeted degradation of transcription factors by TRAFTACs: TRAnscription Factor TArgeting Chimeras. Cell Chemical Biology. 2021,28(5):648-661 e645.
8. Hany,Z.;Meas,H.;Haug,M.;Beckwith,M.;Louet,C.;Ryan,L.; Hu,Z.;Landskron,J.;Nordbo,S.;Tasken,K,;Yin,H.;Damas,J.;Flo. T.; Sensing of HIV-1 by TLR8 activates human T cells and reverses latency. Nature Communication. 2020 Jan 9;11(1):147
9. Xia,T.; Hu,Z.;Ji,W.;Zhang,S.;Shi,H.;Liu,C.;Pang,B.;Liu,G.;Liao,X.;Synthesis of Withasomnine and Pyrazole derivatives via intramolecular dehydrogenative cyclization,as well as biological evaluation of Withasomnine-based scaffolds. Organic Chemistry Frontiers. 2018,5,850-854
10. Moen,S.;Ehrnstrom,B.;Kojen,J.;Yurchenko,Beckwith,K.;Afset,J.;Damas,J.;Hu,Z.;Yin,H.;Espevik,T.;Stenvik,J.;Human Toll-like Receptor 8 (TLR8) is an important sensor of pyogenic bacteria,and is attenuated by cell surface TLR signaling. Frontier in Immunology.10:1209.
11. Ehrnstrom,B.;Kojen,J.F.;Moen,S.H.; Hu,Z.;Damas,J.K.,Mollnes,T.E.;Yin,H.;Espevik,T.;Stenvik J.;TLR8 and complement C5 induce cytokine release and thrombin activation in human whole blood challenged with Gram-positive bacteria. Journal of Leukocyte Biology 2020,107,673–683.
12. Chen,H.#; Hu,Z.#;Tang,C.;Quinn,R.;Feng,Y.;Yao,S.;Ye Y.;Dictamins A–C,three unprecedented apotirucallane-type trinortriterpenoids from Dictamnus dasycarpus.Tetrahedron Letters. 2013,5,4150–4153
13. Qi X.;Wang,L.;Zhu,J.; Hu,Z.;Zhang,J.;Self-double-emulsifying drug delivery system (SDEDDS):A new way for oral delivery of drugs with high solubility and low permeability. International Journal of Pharmaceutics. 2011,409,245–251.
# Co-First Author.