Ph.D.
Graduated in 2022
Ph.D.
Graduated in 2022
Ph.D.
Graduated in 2022
M. S.
Graduated in 2022
M. S.
Graduated in 2022
M. S.
Graduated in 2022
Ph. D.
Graduated in 2021
Ph. D.
Graduated in 2021
Ph. D.
Graduated in 2021
M. S.
Graduated in 2021
M. S
Graduated in 2021
M. S.
Graduated in 2020
M. S.
Graduated in 2020
I obtained my bachelor's degree and joined professor Wu's group in 2017. My research focus on developing new methodologies to improve the stability of peptides as well as precisely regulate and effficient lock of linear peptides into multicyclic topologies with less isomers.
M. S.
Graduated in 2020
I joined the group in Sept. 2017 as a master student. I take the research as a long-distance running which needs to persist. I’m working to screen selective and high affinity inhibitors for proteins implicated in pathologic cell survival by phage display technology and modify peptides that display on the gⅢp of filamentous phage by the chemical post-translational modification.
M. S.
Graduated in 2020
I joined Prof. Wu's research team in September 2017 as a master student. My current research focuses on using dynamic covalent disulfide bonds and hydrazone to build a new trimer which can be used as an efficient linker to enhance stability of proteins.
M. S.
Graduated in 2020
My research focuses on developing unnatural amino acids compatible with solid phase peptide synthesis (SPPS), which can be used for studying structural motifs and functional peptides.
Graduated in 2018
1. Deciphering the molecular mechanism of thiol-mediated disulfide exchange reactions on the cell surface.
2. Develop novel strategies to improve cell uptake based on the thiol-thioether exchange reactions on the cell surface.
Ph. D.
Develop novel tools based on unnatural amino acids (cysteine analogues) and small molecules for peptide modification and cyclization.
Ph. D.
Graduated in 2019
My research focus on designing drug molecules which target specific protein and can escape endosomes.
Ph.D.
Graduated in 2019
Disulfide: nature's gift to chemists. My goal is to decipher the molecular principles that govern precise disulfide pairing and also work to develop a suite of new probes that provide fundamental insight into Disulfide redox-biological fate.
M. S.
Graduated in 2019
Phage display technology as an in vitro selection system is based on the expression of large peptide libraries on the surface of filamentous phage. My work is to screen bicyclic peptides which bind to protein targets with high affinity and selectivity.
M. S.
Graduated in 2019
Ph. D.
Graduated in 2018
Peptides are promising molecular scaffolds for the development of potential therapeutics due to the high affinity and specificity to biomacromolecules. However, inherent instability towards proteolytic digestion limits their applications. My research is to exploit new strategies to improve the secondary structure and proteolytic stability of peptides, then benefit the development of peptide therapeutics and probes.
Graduated in 2018
Graduated in 2018
M. S.
Graduated in 2017
M. S.
Graduated in 2017
M. S.
Graduated in 2017