Shao-Qing Zhang, Ph.D.

2020- Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences 
"Shao-Qing Zhang"
Mean distance: 8.51
Cross-listing: Astronomy Tree


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Wu-pei Su grad student 2006 (Computer Science Tree)
William F. DeGrado grad student 2013 Penn
 (Association of protein helices and assembly of foldamers: Stories in membrane and aqueous environments.)
Bradley T. Hyman post-doc 2020 Massachusetts General Hospital & Harvard Medical School (Neurotree)
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Chino M, Zhang SQ, Pirro F, et al. (2018) Spectroscopic and metal binding properties of a de novo metalloprotein binding a tetrazinc cluster. Biopolymers. e23339
Zhang SQ, Huang H, Yang J, et al. (2018) Designed peptides that assemble into cross-α amyloid-like structures. Nature Chemical Biology
Zhang S, Liu L, Yang J, et al. (2018) De Novo Design of Cross-α Amyloid-Like Fibrils with Cellular Activity Biophysical Journal. 114: 410a
Zhang SQ, Chino M, Liu L, et al. (2017) De Novo Design of Tetranuclear Transition Metal Clusters Stabilized by Hydrogen-Bonded Networks in Helical Bundles. Journal of the American Chemical Society
Polizzi NF, Wu Y, Lemmin T, et al. (2017) De novo design of a hyperstable non-natural protein-ligand complex with sub-Å accuracy. Nature Chemistry. 9: 1157-1164
Kim KH, Ko DK, Kim YT, et al. (2016) Protein-directed self-assembly of a fullerene crystal. Nature Communications. 7: 11429
Yu D, Baird MA, Allen JR, et al. (2015) A naturally monomeric infrared fluorescent protein for protein labeling in vivo. Nature Methods
Walsh JD, Chu S, Zhang SQ, et al. (2015) Design and characterization of swapped-domain constructs of HIV-1 glycoprotein-41 as receptors for drug discovery. Protein Engineering, Design & Selection : Peds. 28: 107-16
Zhang SQ, Kulp DW, Schramm CA, et al. (2015) The membrane- and soluble-protein helix-helix interactome: similar geometry via different interactions. Structure (London, England : 1993). 23: 527-41
Chu S, Kaur H, Nemati A, et al. (2015) Swapped-domain constructs of the glycoprotein-41 ectodomain are potent inhibitors of HIV infection. Acs Chemical Biology. 10: 1247-57
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