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This protocol involves transfecting cAMP sensors and bPAC-nLuc, an optogenetic protein, to accurately track its cellular distribution and response to light stimulation. The innovative approach of creating a cAMP response map using a point scanning system holds the potential for advancing research with optogenetic proteins in different fields.
Our goal was to accurately track the cellular distribution of an optogenetic protein and evaluate its functionality within a specific cytoplasmic location. To achieve this, we co-transfected cells with nuclear-targeted cAMP sensors and our laboratory-developed optogenetic protein, bacterial photoactivatable adenylyl cyclase-nanoluciferase (bPAC-nLuc). bPAC-nLuc, when stimulated with 445 nm light or luciferase substrates, generates adenosine 3',5'-cyclic monophosphate (cAMP). We employed a solid-state laser illuminator connected to a point scanning system that allowed us to create a grid/matrix pattern of small illuminated spots (~1 µm2) throughout the cytoplasm of HC-1 cells. By doing so, we were able to effectively track the distribution of nuclear-targeted bPAC-nLuc and generate a comprehensive cAMP response map. This map accurately represented the cellular distribution of bPAC-nLuc, and its response to light stimulation varied according to the amount of protein in the illuminated spot. This innovative approach contributes to the expanding toolkit of techniques available for investigating cellular optogenetic proteins. The ability to map its distribution and response with high precision has far-reaching potential and could advance various fields of research.
Optogenetics, born as a tool that revolutionized neurosciences, is now a growing research field and a rising technology routinely used by many laboratories worldwide and across various research areas in biology. We developed bPAC-nLuc, a versatile optogenetic protein, by fusing a light-sensitive adenylyl cyclase (AC) from Beggiatoa sp. (bacterial photoactivatable adenylyl cyclase; bPAC) to nanoluciferase (nLuc)1,2,3. When stimulated with blue light, bPAC produces the second messenger 3',5'-cyclic adenosine monophosphate (cAMP). nLuc is a recently developed small lucif....
1. HC-1 cell culture and preparation for imaging
The results presented in Figure 1 show that only stimulations directed to the cell nucleus were able to generate measurable cAMP elevations. This confirms that NLS-bPAC-nLuc is expressed exclusively in the nuclear compartment of HC-1 cells. It is possible to precisely stimulate an optogenetic protein using this grid/matrix pattern to map its intracellular distribution. Additionally, the higher cAMP elevations towards the nuclear center reflect the higher mass.......
The objective of this study was to precisely monitor the intracellular distribution of an optogenetic protein and assess its performance within a particular cytoplasmic compartment. We also showed the precise stimulation capabilities of a point scanning system on cells expressing an optogenetic protein. To achieve this, we employed a nuclear-targeted bPAC-nLuc with high expression levels but a very confined distribution limited to the nucleus. The results showed that stimulation spots separated by only ~1 µm can eit.......
Funding was provided by the National Institutes of Health (NIH) grants R01 GM099775 and GM130612 to D.L.A.
....Name | Company | Catalog Number | Comments |
13 W Amber compact fluorescence bulb - Low Blue Lights | Photonic Developments | ||
3-Isobutyl-1-methylxanthine (IBMX) | Sigma | I7018 | |
6-line multi-LED Lumencor Spectra X | Lumencor | 6-line multi-LED light engine | |
Corning - DMEM | Thermo Fischer | MT10013CMEA | |
Corning - Regular fetal bovine serum | Thermo Fischer | MT35011CV | |
Cover glasses: circles | Thermo Fischer | 12545102P | |
GBX-2 dark red safelight filter 5.5" | Kodak | 1416827 | Red safelight lamp |
Hanks' balanced salt solution (HBSS) 10x | Thermo Fischer | 14185052 | Diluted to 1x, adjusted pH |
LDI-7 | 89 North | ||
L-Glutamine | Thermo Fischer | BW17605E | |
Lipofectamine 3000 | Thermo Fischer | L3000001 | Transfection kit |
Olympus IX83 motorized two-deck microscope | Olympus | Motorized two-deck microscope | |
Opti-MEM, no phenol red | Thermo Fischer | 11058021 | |
ORCA-fusion digital CMOS camera | Hamamatsu | C14440-20UP | |
Penicillin-streptomycin (10,000 U/mL) | Thermo Fischer | 15140122 | |
Phosphate buffered solution (1x) | Lonza | 17516F | |
Prior emission filter wheel and filter sets | Prior Scientific, Inc. | Emission filter wheel | |
Prior Proscan XY stage | Prior Scientific, Inc. | XY stage | |
Slidebook 6 | Intelligent Imaging Innovations | Digital microscopy software | |
SysCon software | SysCon Software | Software provided by the stimulation system | |
UGA-42 Geo | Rapp OptoElectronic | ||
UPlanSApo 100x | Olympus | 100x/1.4 NA oil objective (∞/0.17/FN26.5) | |
ZT458rdc dichroic | Chroma Technology Corp | BS, Wavelength (CWL): 498 nm |
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