Non-invasive real-time in vivo bioluminescence imaging of local CaÂ2+ dynamics in living organisms
AssigneeInstitut Pasteur
InventorsPhilippe Brulet, Kelly Rogers, Sandrine Picaud
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AssigneeInstitut Pasteur
InventorsPhilippe Brulet, Kelly Rogers, Sandrine Picaud
Estimating the term…
The invention relates to a method for optical detection of the dynamics of Ca2+ in a biological system, said method comprising monitoring the photons emitted by a recombinant Ca2+-sensitive polypeptide, which comprises or consists of a chemiluminescent protein linked to a fluorescent protein, present in said biological system. In a particular embodiment, said recombinant polypeptide comprises or consists of the Aequorin and GFP linked by a linker allowing chemiluminescence resonance energy transfer (CRET), and optionally comprises a peptidic fragment capable of targeting said recombinant polypeptide into a specific cellular domain or compartment. The present invention also concerns a transgenic non-human animal expressing said recombinant polypeptide sensitive to calcium concentration, in conditions enabling the in vivo monitoring of Ca2+ dynamics. In a particular embodiment, the expression and/or localization of said recombinant polypeptide is restricted to a specific tissue, a single-cell type and/or in a particular cellular compartment or domain.
A method for the optical detection of Ca2+ signals in a transgenic mouse or rat, wherein the method comprises:
A method for the optical detection of Ca2+ signals in transgenic neonatal or embryonic mice or rats, wherein the method comprises:
Dependencies are inferred from the claim text.