副研究员/高级工程师
赵东东

赵东东


  • 职  称:副研究员
  • 学  历:硕士研究生
  • 通讯地址:天津市空港经济区西七道32号
  • 电  话:022-24828783
  • 邮政编码:300308
  • 电子邮件:zhao_dd@tib.cas.cn
  • 部  门:合成生物技术研究组

简历

2021-至今,中国科学院天津工业生物技术研究所,副研究员

2016-2021,中国科学院天津工业生物技术研究所,助理研究员

2014-2016,中国科学院天津工业生物技术研究所,研究实习员

2011-2014,中国食品发酵工业研究院,发酵工程,研究生/硕士

2007-2011,山东大学,生物技术,本科/学士

研究方向

基因编辑技术开发与应用

获奖及荣誉

2022 入选中国科学院青年创新促进会会员

代表成果

1.Zhao D, Li J, Li S, Xin X, Hu M, Marcus A. Price, Susan J. Rosser, Bi C, Zhang X. Glycosylase base editors enable C-to-A and C-to-G base changes.Nature Biotechnology.2021, 39:35–40.

2. Ye L, Zhao D, Li J, Wang Y, Li B, Yang Y, Hou X, Wang H, Wei Z, Liu X, Li Y, Li S, Liu Y, Zhang X, Bi C. Glycosylase-based base editors for efficient T-to-G and C-to-G editing in mammalian cells. Nature Biotechnology. 2023, 10.1038/s41587-023-02050-w.(共同一作)

3. Zhao D, Jiang G, Li J, Chen X, Li S, Wang J, Zhou Z, Pu S, Dai Z, Ma Y, Bi C, Zhang X. Imperfect guide-RNA (igRNA) enables CRISPR single-base editing with ABE and CBE. Nucleic Acids Research. 2022, 50:4161-4170.

4. Zhao D, Zhu X, Zhou H, Sun N, Wang T, Bi C, Zhang X. CRISPR-based metabolic pathway engineering. Metabolic Engineering. 2021, 63:148-159.

5. Wu Y, Wan X, Zhao D, Chen X, Wang J, Tang X, Li J, Li S, Sun X, Bi C, Zhang X. AAV-mediated base-editing therapy ameliorates the disease phenotypes in a mouse model of retinitis pigmentosa. Nature Communications. 2023, 14:4923.(共同一作)

6. Sun N, Zhao D, Li S, Zhang Z, Bi C, Zhang X. Reconstructed glycosylase base editors GBE2.0 with enhanced C-to-G base editing efficiency and purity. Molecular Therapy. 2022, 30(7),2452-2463.(共同一作)

7. Wang P, Zhao D, Li J, Su J, Zhang C, Li S, Fan F, Dai Z, Liao X, Mao Z, Bi C, Zhang X. Artificial diploid Escherichia coli by a CRISPR chromosome- doubling technique. Advanced Science. 2023, 10 (7).(共同一作)

8. Wang J, Zhao D, Li J, Hu M, Xin X, Price MA, Li Q, Liu L, Li S, Rosser SJ, Zhang C, Bi C, Zhang X. Helicase-AID. A novel molecular device for base editing at random genomic loci. Metabolic Engineering. 2021, 67:396-402.(共同一作)

9. Zhu X, Zhao D, Qiu H, Fan F, Man S, Bi C*, Zhang X*. The CRISPR/Cas9-facilitated multiplex pathway optimization (CFPO) technique and its application to improve the Escherichia coli xylose utilization pathway. Metabolic Engineering. 2017, 43:37-45.(共同一作)

10. Zhao D, Yuan S, Xiong B, Sun H, Ye L, Li J, Zhang X, Bi C. Development of a fast and easy method for Escherichia coli genome editing with CRISPR/Cas9. Microbial Cell Factories. 2016, 15:205.