Wenshe Ray Liu

Wenshe Ray Liu

Department of Chemistry, Texas A&M University

Affiliated withTexas A&M University

Research Area

Biography

Dr. Wenshe Liu received his BS degree from Peking University in 2000 and his Ph.D. degree under the supervision of Dr. Michael D. Toney from University of California-Davis in 2005. Following two years of postdoctoral training in Dr. Peter G. Schultz group in the Scripps Research Institute, he started his independent research group as an assistant professor at Texas A&M University in 2007. Dr. Liu was promoted to the associate professor rank in 2013 and furthered to the full professor rank in 2016. He is currently holding the Emile and Marta Schweikert endowed professorship in the Texas A&M Chemistry Department. Dr. Liu was originally trained to work on both enzymology and protein crystallography during his Ph.D. study and later switched to organic chemistry and molecular biology during his postdoctoral training. His current research group has two operating branches. One is organic synthesis and the other is molecular and biological chemistry. The technical basis of research in Liu group is the amber suppression based noncanonical amino acid mutagenesis, targeted questions being different. One focus is to build methods for the synthesis of chromatin with specific lysine modifications for the illustration of how these modifications influence chromatin structures, interactions with transcription factors, recognition by epigenetic enzymes, and the control of other modifications in chromatin. The second focus is to develop techniques for integrating one or two noncanonical amino acids into phage displayed peptide libraries. These noncanonical amino acids serve as active chemical handles to cyclize peptide libraries, anchor enzyme/protein active sites, and expand chemical diversities of libraries by reacting with other small molecules. The ultimate goal of this research direction is to identify tight and selective inhibitors of epigenetic enzymes that can be applied for cancer treatment.

JoVE Journal Publications

ArticleTotal : 1
Year
Site Specific Lysine Acetylation of Histones for Nucleosome Reconstitution using Genetic Code Expansion in <em>Escherichia coli</em>
Publication title

Cited by 1

2020

Other Publications

Article
Year
Synthesis of proteins with defined posttranslational modifications using the genetic noncanonical amino acid incorporation approach.

Molecular bioSystems| PubMed ID: 21088799

2011
The genetic incorporation of thirteen novel non-canonical amino acids.

Chemical communications (Cambridge, England)| PubMed ID: 24473369

2014
The nitrilimine-alkene cycloaddition is an ultra rapid click reaction.

Chemical communications (Cambridge, England)| PubMed ID: 24519550

2014
2014
A genetically encoded aldehyde for rapid protein labelling.

Chemical communications (Cambridge, England)| PubMed ID: 24756176

2014
Genetically encoded unstrained olefins for live cell labeling with tetrazine dyes.

Chemical communications (Cambridge, England)| PubMed ID: 25224663

2014
Phospha-Michael Addition as a New Click Reaction for Protein Functionalization.

Chembiochem : a European journal of chemical biology| PubMed ID: 26756316

2016
The "π-Clamp" Offers a New Strategy for Site-Selective Protein Modification.

Chembiochem : a European journal of chemical biology| PubMed ID: 26928847

2016
2016
2018
2019
Covalent Inhibition in Drug Discovery.

ChemMedChem| PubMed ID: 30816012

2019
A Genetically Encoded, Phage-Displayed Cyclic-Peptide Library.

Angewandte Chemie (International ed. in English)| PubMed ID: 31398275

2019
2020
2020
Expressed Protein Ligation without Intein.

Journal of the American Chemical Society| PubMed ID: 32212692

2020
Targeting the SARS-CoV-2 Main Protease to Repurpose Drugs for COVID-19.

bioRxiv : the preprint server for biology| PubMed ID: 32511370

2020
2020
An optimal "Click" formulation strategy for antibody-drug conjugate synthesis.

Bioorganic & medicinal chemistry| PubMed ID: 33071032

2020
2020