Yi XUE     Ph.D.

Assistant Professor


1993-1997        B.S.                Tsinghua University, Modern Applied Physics

1997-1999        Engineer        Start Computer Company

2000-2003        M.S.                Tsinghua University, Biological Science and Biotechnology

2004-2009        Ph.D.              Purdue University, Chemistry

2010-2013        Postdoc          Purdue University

2013-2016        Postdoc          University of Michigan; Duke University

2016-present    Assistant Professor, Associate Professor                    Tsinghua University

 

Research interest


Our primary research interests are focused on characterizing structure and dynamics of non-coding RNAs and intrinsically disordered proteins using solution NMR spectroscopy and computational approaches such as MD simulations. We aim to develop novel NMR techniques, labeling methods, and computational tools to study three-dimensional structure and conformational switch of large non-coding RNAs and ribonucleoproteins, which pose a significant challenge to existing methods. We are also interested in reconstructing conformational motion of highly flexible biomolecules, as well as ensemble-based virtual drug screening.


Selected publications


1. Han, G. and Xue, Y.# (2022). Rational design of hairpin RNA excited states reveals multi-step transitions. Nat. Commun. 13, 1523

2. Cao, J. and Xue, Y.# (2021). Characteristic chemical probing patterns of loop motifs improve prediction accuracy of RNA secondary structures. Nucleic Acids Res. 49, 4294-4307

3. Wang, Y., Han, G., Jiang, X., Yuwen, T. and Xue, Y.# (2021). Chemical shift prediction of RNA imino groups: application toward characterizing RNA excited states. Nat. Commun. 12, 1595

4. Li, W., Kou, J., Qin, J., Li, L., Zhang, Z., Pan, Y., Xue, Y.# and Du, W.# (2021). NADPH levels affect cellular epigenetic state by inhibiting HDAC3–Ncor complex. Nat. Metab. 3, 75-89

5. Song, Y., Zhang, Y., Pan, Y., He, J., Wang, Y., Chen, W., Guo, J., Deng, H., Xue, Y.#, Fang, X.# and Liang, X.# (2020). The microtubule end-binding affinity of EB1 is enhanced by a dimeric organization that is susceptible to phosphorylation. J. Cell Sci. 133, jcs241216



Contact information


Email: yixue@mail.tsinghua.edu.cn

Phone: +86-10-62784766 (lab)