calcium Flashcards
L type voltage gated calcium channel
open for long periods of time, found in skeletal muscle and cortex
T type voltage gated calcium channel
open for short periods of time, found in the heart and thalamus
N type voltage gated calcium channel
open for long periods of time, high conductance, found throughout the CNS and PNS
P type voltage gated calcium channel
high voltage activated, found in Purkinje cells in cerebellum
Ca2+ imaging
measures how much Ca2+ enters the cell
Ca2+ indicators
fluoresce when bound to Ca2+, more fluorescence = more intracellular Ca2+ = more neural activity
-can be chemical or GECI’s
chemical calcium indicators
small molecules that selectively chelate Ca2+, low specificity and short period of action
-dyes injected into a target region and diffuse into every cell type in the area before their fluorescence is recorded during intracellular calcium waves
genetically encoded calcium indicators (GECIs)
fluorescent proteins derived from GFP fused with calmodulin or troponin C, genes encoding these proteins are transfected into cell lines
- can be selective for cellular subtypes
- long term in vivo imaging
aequorin
the first GECI, requires coelenterazine, a photoprotein found in jellyfish, fluoresces when bound to free calcium
- wasn’t specific to calcium
- unstable in pH environments
- requires consumption of coelenterazine which is only found in marine animals (doesn’t work in mammals)
probes using fluorescence resonance energy transfer (FRET)
a more versatile category of GECI
- genetic calcium indicators derived from GFP
- utilized two fluorescent molecules that when bound to calcium, moved closer together and emitted a specific wavelength of light
- power of technique is low
probes that utilize conformational changes of GFP
- GECI category, have limited signal intensity (bad spatial and temporal resolution)
- protein only fluoresced after calcium binding induced a conformational change in the GFP protein itself
- signal to noise ratio was too high
G-CaMP
-GECI - calcium probe based on a single GFP molecule with high calcium affinity and intensity, fluoresces when calcium binds to calmodulin inducing a conformational change in cpEGFP (tightens up)
limitations of a confocal/two photon microscope (for in vivo microscopy of Ca2+ imaging)
- a two photon microscope can only penetrate 1mm of brain tissue before light is scattered and signal is lost (can only measure cortical activity)
- need to head fix the animal (restriction of movement)
fibre miniscope
measures Ca2+ wave recordings in freely moving animals
- heavy, movements were limited
- very little depth of light penetration
- cannot measure single cell activity
fiber optics
-implanted single multimode fibre