个人简介
林琳,女,教授,主要从事生物医药,分子生物学,蛋白质工程方向研究。
教育经历
1981.9-1985.6 辽宁大学 环境生物学专业 本科
1997.9-2001.6 福建农林大学 植物病理学专业 博士
2004.8-2016.3 哈佛大学医学院 医学专业 博士后
主要参与的项目
1.工业微生物高通量选育与保藏技术研发平台建设,2006H0085,主持;
2.扩展青霉碱性脂肪酶基因克隆、表达及突变体研究,B0120001,主持
3.洗涤剂配套酶制剂―碱性脂肪酶研究,96c-03-02-01,主持
4.Structural Aspects of Urokinase Receptor in Vascular Biology,RO1 5R01HL086584-03,参加
5.Thrombus formation in vivo,PO1 HL087203,参加
6.Program in blood coagulation and vascular biology,T32 5T32HL007917-14,参加
7.Protein disulfide isomerases: A new class of antithrombotic targets,1U54HL112302-01,参加
8.Thiol Isomerases in Hemostasis and Thrombosis,5R35Act HL135775,参加
9.Biomarkers and mechanisms in cancer associated thrombosis,5TU01 Act HL143365,参加
主要成果
1.Liu M*, Lin L*(co-first), Høyer-Hansen G, Ploug M, Li H, Jiang L, Yuan C, Li J, Huang M. Crystal structure of the unoccupied murine urokinase-type plasminogen activator receptor (uPAR) reveals a tightly packed DII-DIII unit. FEBS Lett. 2019 Jun;593(11):1236-1247
2.Yunbin Jiang, Lin Lin*(co-coresponding)Shanli Chen, Longguang Jiang, Mette C. Kriegbaum, Henrik Gårdsvoll, Line V. Hansen, Jinyu Li, Michael Ploug, Yuan Cai, Mingdong Huang*. Crystal Structures of Human C4.4A Reveal the Unique Association of Ly6/uPAR/α-neurotoxin Domain。International Journal of Biological Sciences 2020; 16(6): 981-993.
3.Lin Lin, Blocking the b'x domain of PDI interferes with its interaction with aIIbb3 and prevents thrombus formation. International Society on Thrombosis and Haemostasis (ISTH) 2017 Congress July 8 to 13, 2017, Berlin, German (oral presentation)
4.Chen, Shanli(#); Lin, Lin(#) (co first); Yuan, Cai; Gardsvoll, Henrik; Kriegbaum, Mette C.; Ploug, Michael; Huang, Mingdong. Expression and crystallographic studies of the D1D2 domains of C4.4A, a homologous protein to the urokinase receptor Acta Crystallographica Section F-Structural Biology Communications, 2017.8, 73: 486~490
5.Lin Lin, Srila Gopal, Anish Sharda, Freda Passam, Sheryl R. Bowley, Jack Stopa, Guangpu Xue, Cai Yuan, Barbara C. Furie, Robert Flaumenhaft, Mingdong Huang, Bruce Furie,Quercetin-3-rutinoside inhibits protein disulfide isomerase by binding to its b'x domain. J. Biol. Chem. 2015 290: 23543-23552