Introducing Our Authors - American Chemical Society

Oct 20, 2017 - Sciences, B.Sc. Molecular Medicine and Biochemistry, 2012,. Advisor: Dr. Jody Mason. Current Position: ... Education: Jilin University,...
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Introducing Our Authors Cite This: ACS Chem. Biol. 2017, 12, 2475-2476





DANIEL BAXTER

pubs.acs.org/acschemicalbiology

BOQUN LIU

Image courtesy of Liam Baxter.

Image courtesy of Yanglei Yi.

Education: University of Essex, U.K., School of Biological

Education: Jilin University, Department of Food Science and

Sciences, B.Sc. Molecular Medicine and Biochemistry, 2012,

Technology, B.S. Food Science and Engineering, 2010; Jilin

Advisor: Dr. Jody Mason Current Position: Ph.D. graduand, Department of Biology

University, Laboratory of Nutrition and Functional Food, M.S. Food Science, 2013, Supervisor: Prof. Jingbo Liu Current Position: Ph.D. student in Biophysics, Groningen

and Biochemistry at the University of Bath, U.K., Advisor: Dr. Jody Mason Nonscientific Interests: Traveling and experiencing nature

Biomolecular Sciences and Biotechnology Institute, University of

and people in different places, hiking and adventuring, and

Boersma Nonscientific interests: Photography, table tennis, and

Groningen, Supervisors: Prof. Bert Poolman and Dr. Arnold

generally enjoying life My research interests focus on the exploitation and development of library selection systems to isolate novel peptides

football My research focuses on the biophysical properties of the

that can modulate the activities of therapeutically interesting

cytoplasm, especially on the quantification of macromolecular

protein targets and chemical modification of these peptides

crowding as well as ionic strength in living cells with novel

toward valuable therapeutic applications. In our paper, we take

Fö rster resonance energy transfer (FRET) sensors. Ionic strength influences a wide array of electrostatic interactions

a peptide antagonist of oncogenic activator protein-1 (AP-1)

including protein activity, (macro)-molecule associations/

isolated by an in cellulo protein-fragment complementation

aggregations, and other processes. To detect the ionic strength,

assay (PCA) and successfully truncate it to a more attractive

we designed the first ionic strength sensors in living cells.

size while maintaining the majority of its binding affinity.

The sensors are based on FRET and contain a positively

This is achieved through the entropic preorganization effects of

and a negatively charged α-helix with electrostatic attraction

covalent lactam helix constraints. We further demonstrate

that will depend on the ionic strength. With these sensors,

that this peptide can be delivered to breast cancer cells

researchers will be able to track the intracellular ionic strength

where it effectively reduces proliferation. This strategy holds

on the single-cell level in changing environments or intra-

considerable promise for the future development of drugs against

cellular conditions. (Read Liu’s article DOI: 10.1021/acschem-

AP-1 and other transcription factors less amenable to small

bio.7b00348.)

molecule modulation. (Read Baxter’s article DOI: 10.1021/ acschembio.7b00693.)

Published: October 20, 2017 © 2017 American Chemical Society

2475

DOI: 10.1021/acschembio.7b00858 ACS Chem. Biol. 2017, 12, 2475−2476

ACS Chemical Biology



Introducing Our Authors

WEI XU

Image courtesy of Yuhui Sun.

Education: Wuhan University, School of Pharmaceutical Sciences, B.Sc. Pharmaceutical Science, 2011; Wuhan University, School of Pharmaceutical Sciences, Ph.D. Molecular Biology and Biochemistry, 2017, Advisor: Prof. Yuhui Sun Current Position: Ph.D. School of Pharmaceutical Sciences, Wuhan University, Advisor: Prof. Yuhui Sun Nonscientific Interests: Cycling, photography, and computer programming My project is focused on the discovery of novel natural products with bioactivities and elucidation of their biosynthetic mechanism. During a bioassay-guided Streptomyces discovery, a brick-red color Streptomyces spectabilis CCTCC M2017417 showed significant antimethicillin-resistant Staphylococcus aureus (MRSA) activity. To characterize the active compounds and their biosynthetic process, a detailed genome sequencing and assembly were performed. Then, I localized a gene cluster corresponding to the biosynthesis of streptovaricins, which are the main anti-MRSA activity contributors in this strain. A biosynthetic pathway was proposed, and P450 genes in this cluster were functionally analyzed. My scientific interests are mainly concentrated on rational utilization of polyketide synthases to build high-profit molecules in microbes and automatic regulation of the biosynthesis process in natural or heterologous hosts with the help of genetic circuits. (Read Xu’s article DOI: 10.1021/acschembio.7b00467.)

2476

DOI: 10.1021/acschembio.7b00858 ACS Chem. Biol. 2017, 12, 2475−2476