The ability to optically record neuronal electrical activity with the temporal and fine-feature waveform resolution on par with whole-cell patch clamp electrophysiology would permit the correlation, of the physiology of individual cells and cell types, to the neural circuit-level activity that underlies behaviors, cognition, and affective states observed in the normal and diseased brain. Genetically encoded voltage indicators (GEVIs) hold great promise for this purpose as cell-type specific probes, if their voltage-sensitivity, brightness, and temporal resolution can be engineered to provide the reliable detection of high frequency action potentials, the detection of sub-threshold ?minis? critical to synaptic scaling and homeostatic plasticity, and the ability to resolve waveforms useful for deducing specific channel/receptor contributions to spiking and synaptic transmission. We propose to invent next-generation GEVIs through rational design from first principles of non- biologically derived proteins. We will adapt artificial protein ?maquettes,? which are de novo-designed and rigid 4-helix bundle proteins that serve as custom scaffolds for arbitrarily positioning biological co-factors within the scaffold core. Strategic positioning of a biliverdin chromphore within a transmembrane maquette allows for voltage sensing by the optical Stark effect, in which chromophores exhibit electric field-induced changes in absorbance that result in ultrafast changes in observed fluorescence. We call these proteins, ?MASTERs? (Maquette Stark Effect Reporters). The ultrafast infrared-fluorescent reporters will recapitulate whole-cell recordings with no observable delay or waveform difference.

Public Health Relevance

RELEVANCY STATEMENT: The ability to optically record neuronal electrical activity with the temporal and fine-feature waveform resolution on par with whole-cell patch clamp electrophysiology would permit the correlation, of the physiology of individual cells and cell types, to the neural circuit-level activity that underlies behaviors, cognition, and affective states observed in the normal and diseased brain. To this end, we propose to invent next-generation genetically encoded voltage indicators (GEVIs) through rational design of non-biologically derived proteins, specifically de novo protein ?maquettes? that report voltage by the optical Stark effect, which is an intrinsically fast and voltage-dependent spectral change.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS101106-03
Application #
9690202
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Leenders, Miriam
Project Start
2017-05-01
Project End
2022-04-30
Budget Start
2019-05-01
Budget End
2020-04-30
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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Glantz, Spencer T; Berlew, Erin E; Jaber, Zaynab et al. (2018) Directly light-regulated binding of RGS-LOV photoreceptors to anionic membrane phospholipids. Proc Natl Acad Sci U S A 115:E7720-E7727