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. 2017 Dec 11;25(3):542–572. doi: 10.1038/s41418-017-0020-4

Table 5.

Several genetically encoded fluorescent and bioluminescent reporters of Ca2+ with varying affinities (Kd) that have been successfully targeted to neuronal mitochondria

Reporter name Reporter detail Excitation, emission wavelengths (nm) Dissociation constant, Kd (μM) References
Rhod-2 Fluorescent molecule λex, ~557 0.6* [112]
λem, ~581
4mtD2cpv Yellow cameleon (FRET) CFP (ECFP): λex/λem, 435/475 4mtD2cpv: 0.1, 7.7 [112, 122]
4mtD3cpv YFP (cp173Venus): λex/λem, 515/527 4mtD3cpv: 0.76
4mtD4cpv 4mtD4cpv: 49.7
mtAEQmut Aequorin (bioluminescence) λem, 465 Varying affinities [122] [123, 124]
Mit-GEM-GECO-1 Single FP, dual emission, ratiometric λex, 390 0.34 [53, 102, 129]
λem, 455, 511
Mito-LAR-GECO1.2 Single FP (RFP) λex, 557 12 [130]
λem, 584
mito-GCaMP2 Single FP (cpEGFP) λex, 489 0.2 [112, 126, 127]
λem, 509
mt-RCaMP Single FP (cp-mRuby) λex, 570 1.6 [128]
λem, 590
mtPericam Dual-excitation, ratiometric λex, 415, 494 1.7 [100, 125]
λem, 515

Publications refer to the work that originally generated the probe and/or studies where the probe was utilised in neuronal mitochondria. Multiple mitochondria-localised Ca2+ reporters based on GCaMP have been generated

aRhod-2 analogues have varying affinities