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郭强

 

 

郭强

 

 

电子邮箱:guo.qiangatpkudotedudotcn

 

研究方向:

 
我们是原位结构生物学实验室。关注“细胞建筑学”:各个亚细胞结构是如何搭建成一个具有完整生物学功能的细胞,以及“生物大分子社会学”:细胞内的细胞器、生物大分子之间的相互关系。
 
原位结构生物学是基于冷冻光电联用(CLEM)、冷冻电子断层扫描(cryo-ET)等技术的新兴结构生物学分支,是一种可以在细胞生理状态下,对生物大分子和亚细胞结构在分子分辨率(1 ~ 10 nm)水平进行原位的结构分析和功能研究的技术手段。 我们主要研究方向包括:
 
1. 在纳米、亚纳米尺度对基础细胞生物学问题的研究。
2. 对包括神经退行性疾病在内的老龄化疾病致病机制的研究。
3. 适用于组织样品的高分辨原位结构生物学方法优化。
 

 

代表性论文:

 

1.    Yasuda, S., Tsuchiya, H., Kaiho, A., Guo, Q., Ikeuchi, K., Endo, A., Arai, N., Ohtake, F., Murata, S., Inada, T., et al. (2020). Stress- and ubiquitylation-dependent phase separation of the proteasome. Nature 578, 296–300.

2.    Guo, Q., Bin, H., Cheng, J., Seefelder, M., Engler, T., Pfeifer, G., Oeckl, P., Otto, M., Moser, F., Maurer, M., Pautsch, A., Baumeister, W., Fernandez-Busnadiego, R., Kochanek, S. (2018). The cryo-electron microscopy structure of huntingtin. Nature 555, 117–120.

3.    Guo, Q., Lehmer, C., Martinez-Sanchez, A., Rudack, T., Beck, F., Hartmann, H., Hipp, M.S., Hartl, F.U., Edbauer, D., Baumeister, W., Fernandez-Busnadiego, R. (2018) In Situ Structure of Neuronal C9orf72 Poly-GA Aggregates Reveals Proteasome Recruitment. Cell 172, 696-705.e612.

4.    Zhao, Y., Zeng, X., Guo, Q., and Xu, M. (2018). An integration of fast alignment and maximum-likelihood methods for electron subtomogram averaging and classification. Bioinformatics 34, i227–i236

5.     Li, Z., Guo, Q., Zheng, L., Ji, Y., Xie, Y.T., Lai, D.H., Lun, Z.R., Suo, X., and Gao, N. (2017). Cryo-EM structures of the 80S ribosomes from human parasites Trichomonas vaginalis and Toxoplasma gondii. Cell Res 27, 1275-1288.

6.     Feng, B., Mandava, CS., Guo, Q., Wang, J., Cao, W., et al. (2014) Structural and Functional Insights into the Mode of Action of a Universally Conserved Obg GTPase. PLoS Biol 12(5): e1001866.

7.    Yang, Z., Guo, Q., Goto, S., Chen, Y., Li, N., Muto, A., Himeno, H., Deng, H., Lei, J., and Gao, N. (2014). Characterization of the in vivo 30S ribosomal assembly intermediates reveals essential role of S5 and location of unprocessed ends of the 17S rRNA. Protein Cell 5, 394-407.

8.     Li, N., Chen, Y., Guo, Q., Zhang, Y., Yuan, Y., Ma, C., Deng, H., Lei, J., and Gao, N. (2013). Cryo-EM structures of the late-stage assembly intermediates of the bacterial 50S ribosomal subunit. Nucleic Acids Res 41, 7073-7083.

9.    Guo, Q., Goto, S., Chen, Y., Feng, B., Xu, Y., Muto, A., Himeno, H., Deng, H., Lei, J., and Gao, N. (2013). Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM and general features of the assembly process. Nucleic Acids Res 41, 2609-2620. 

10. Guo, Q., Yuan, Y., Xu, Y., Feng, B., Liu, L., Chen, K., Sun, M., Yang, Z., Lei, J., and Gao, N. (2011). Structural basis for the function of a small GTPase RsgA on the 30S ribosomal subunit maturation revealed by cryoelectron microscopy. Proc Natl Acad Sci U S A 108, 13100-13105.

 

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