- Max Planck Croucher Postdoctoral Fellowship in 2020 at Max Planck Institute for Biophysical Chemistry
- Scholarship in 2016 at Max Planck Institute for Biophysical Chemistry
***Nick's latest work on Science uncovered why is the chromosome segregation machinery so error-prone in human eggs and how we could fix that. ***
Media coverage of Nick:
Chun So (Nick) received his B.Sc. in Cell and Molecular Biology (CMB) (first-class honour) from the CUHK in 2016 and his Dr. rer. nat. in Physics of Biological and Complex Systems (summa cum lauda) at the Georg-August-Universität Göttingen in 2019.
Interested in both chemistry and biology, he gained his first two lab experience at the CUHK under the supervision of Prof KS Chan and Prof SY Tsang during his high school education at the La Salle College. By the time of the release of HKDSE results, he made a tough decision between studying chemistry, biology and medicine. At last, he decided to go for the new, appealing, research-oriented CMB programme at the CUHK.
During his undergraduate study, he received 15 awards and scholarships including the Swire Scholarship 2013-2016 and the Fung Scholarship 2015-2016, covering all of his tuition fees and expenses. Apart from studying during the term time, he followed Prof SY Tsang again in his sophomore year and conducted almost-full-time research in her lab. In the past three years, he received excellent guidance from Prof SY Tsang and led a research project on the molecular and cellular mechanisms linking diabetes and breast cancer. He also collaborated with other labmates on studying reverse apoptosis in breast cancer cells and the roles of different TRP channels in mouse embryonic stem cells and cardiac differentiation.
Before making another critical decision in his life, that is, what to study for his PhD, he exposed himself to many different fields in life sciences. By the end of his freshman year, he joined Prof PC Shaw's lab under the SMART program and studied novel proteins of influenza A virus. Later in the summer of his freshman year, he was selected into the Study Abroad Program in Shanghai co-organized by the Harvard University and the Fudan University, working on epithelial-mesenchymal transition in hepatocellular carcinoma in Prof LX Qin's lab. In the summer of his sophomore year, he enrolled in the UROPS of the National University of Singapore and examined small RNAs in neural development in Prof QD Hu's lab. In the summer of his junior year, he was chosen as one of the six students from China in the NDM Summer Internship Programme of the University of Oxford. Under the supervision of Prof L Dorrell, he was exceptionally allowed to work in the containment level 3 facility and helped developing novel T cell receptor-based HIV therapy. In a collaboration between Prof. L Dorrell and Dr N Ternette, he used cutting-edge proteomics to investigate the kinetics of HIV protein during early infection as well. In the summer of his final year, he participated in the TIGP IIP at the Academia Sinica and studied yeast's pre-mRNA splicing in Dr SC Cheng's lab.
Being heavily exposed to different areas of developmental biology, it is not particularly surprising that he continued his doctoral study on even earlier developmental events. In 2016, he received the Croucher Scholarship for Doctoral Study to follow Dr M Schuh to develop new tools for studying different mammalian eggs, including human, and study phase separation during meiotic spindle assembly. Nick's PhD work was highly recognized by the Max Planck Society and the German Society for Cell Biology, leading him to the Otto Hahn Medal, the prestigious Otto Hahn Award and the Nikon Young Scientist Award.
After Nick obtained his doctoral degree, he continued as a postdoc in Dr M Schuh's lab. More recently, he is awarded the Max Planck Croucher Postdoctoral Fellowship to develop new model systems for studying earlier stages of female germline development in Dr M Schuh's and Dr U Günesdogan's lab. Here, he would like to thank the Croucher Foundation again for continuously funding his exciting research in Goettingen, Germany.
Starting from September 2022, Nick will lead an independent research group at the National Institute of Biological Sciences in Beijing, China.
For more information on his previous and current work, please refer to the following publications:
So C, Menelaou M*, Uraji J*, Harasimov K, Steyer AM, Seres KB, Bucevičius J, Lukinavičius G, Möbius W, Sibold C, Tandler-Schneider A, Eckel H, Moltrecht R, Blayney M, Elder K, Schuh M. Mechanism of spindle pole organization and instability in human oocytes. Science 2022 Feb;375(6581):eabj3944. (*equal contribution)
So C*, Cheng S*, Schuh M. Phase separation during germline development. Trends Cell Biol. 2021 Apr;31(4):254-268. (*equal contribution)
Chan YW*, So C*, Yau KL, Chiu KC, Wang X, Chan FL, Tsang SY. Adipose-derived stem cells and cancer cells fuse to generate cancer stem cell-like cells with increased tumorigenicity. J Cell Physiol. 2020 Oct;235(10):6794-6807. (*equal contribution)
So C*, Seres KB*, Steyer AM, Mönnich E, Clift D, Pejkovska A, Möbius W, Schuh M. A liquid-like spindle domain promotes acentrosomal spindle assembly in mammalian oocytes. Science 2019 Jun;364(6447):eaat9557. (*equal contribution)
Xu Y, So C, Lam HM, Fung MC, Tsang SY. Flow cytometric detection of newly-formed breast cancer stem cell-like cells after apoptosis reversal. J Vis Exp. 2019 Jan;(143).
Clift D*, So C*, McEwan WA, James LC, Schuh M. Acute and rapid degradation of endogenous proteins by Trim-Away. Nat Protoc. 2018 Oct;13(10):2149-2175. (*equal contribution)
Xu Y, So C, Lam HM, Fung MC, Tsang SY. Apoptosis reversal promotes cancer stem cell-like cell formation. Neoplasia 2018 Mar;20(3):295-303.
Yang H, Buisson S, Bossi G, Wallace Z, Hancock G, So C, Ashfield R, Vuidepot A, Mahon T, Molloy P, Oates J, Paston SJ, Aleksic M, Hassan N, Jakobsen BK, Dorrell L. Elimination of HIV-1 reservoir cells from antiretroviral therapy-suppressed subjects by engineered immune-mobilising T cell receptors. Mol Ther. 2016 Nov; 24(11):1913-1925.
Lo IC, Chan HC, Qi Z, Ng KL, So C, Tsang SY. TRPV3 channel negatively regulates cell cycle progression and safeguards the pluripotency of embryonic stem cells. J Cell Physiol. 2016 Feb;231(2):403-13.
Qi Y, Qi Z, Li Z, Wong CK, So C, Lo IC, Huang Y, Yao X, Tsang SY. Role of TRPV1 in the differentiation of mouse embryonic stem cells into cardiomyocytes. PLoS One 2015 Jul;10(7):e0133211.