Dr. Wayland Cheng is a cardiothoracic anesthesiologist with the long-term goal of being an independent investigator in anesthetic pharmacology. His research background is in the field of ion channel biophysics, and his interest is in the interaction of anesthetics with pentameric ligand gated ion channels (pLGICs) with a focus on neurosteroids. Neurosteroids are endogenous brain sterols that potently modulate GABAA receptors (GABAARs), and are being developed as anesthetics or treatments of neurologic and psychiatric disorders. Although neurosteroid modulation of the GABAAR has been well characterized, neurosteroid binding to the GABAAR is not well understood. A detailed understanding of the stoichiometry/site(s), orientation and pharmacology of neurosteroid binding to the GABAAR is essential for structure-based drug design. To address this deficiency, the candidate will apply photo-affinity labeling with an existing library of neurosteroid photolabeling reagents, and top-down mass spectrometry (MS), a technique that analyzes intact membrane proteins, to characterize neurosteroid photolabeling of the GABAAR.
Aim 1 is to determine the stoichiometry/site(s), orientation and pharmacophore of neurosteroid photolabeling of ELIC-GABAAR chimeras (tractable model proteins where the transmembrane domain consists of GABAAR subunits).
Aim 2 is to determine the stoichiometry of neurosteroid photolabeling of ?1?3?2 GABAARs proteoforms (intact proteins and all associated modifications), and to test whether certain proteoforms are preferentially photolabeled by neurosteroids. This work will yield novel insights into the structural basis of neurosteroid binding to the GABAAR. It will also establish a generalizable method using top-down MS for characterizing small molecule photolabeling of membrane proteins, and is anticipated to lead to sustainable R01-level funding. This research will be conducted under the mentorship of Dr. Alex Evers, an expert in anesthetic pharmacology, photo-affinity labeling and bottom-up mass spectrometry. The candidate will also be working closely with Dr. Michael Gross and Dr. Julian Whitelegge, both renowned leaders in top-down MS of membrane proteins. The Anesthesiology Department at Washington University provides a robust environment for research in molecular pharmacology. Furthermore, the candidate utilizes an Elite mass spectrometer owned by Dr. Evers, and has full access to the Washington University NIH NIGMS Mass Spectrometry Research Resource led by Dr. Gross, which provides state-of-the-art MS technology for high mass and high resolution measurements.

Public Health Relevance

Neurosteroid analogues are potent modulators of GABAA receptors in the brain, and are being developed as anesthetics or treatments of neurologic and psychiatric diseases. This proposal will provide insights into the structural basis of neurosteroid binding to the GABAA receptor. These insights will advance our fundamental knowledge of neurosteroid mechanisms of action in the GABAA receptor, and may inform structure-based design of neurosteroid-based analogues that target GABAA or other neural receptors.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08GM126336-02
Application #
9566253
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Cole, Alison E
Project Start
2017-09-20
Project End
2021-08-31
Budget Start
2018-09-01
Budget End
2019-08-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Washington University
Department
Anesthesiology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Cheng, Wayland W L; Chen, Zi-Wei; Bracamontes, John R et al. (2018) Mapping two neurosteroid-modulatory sites in the prototypic pentameric ligand-gated ion channel GLIC. J Biol Chem 293:3013-3027