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. Author manuscript; available in PMC: 2015 Jan 13.
Published in final edited form as: Angew Chem Int Ed Engl. 2013 Nov 27;53(3):875–878. doi: 10.1002/anie.201308816

Table 1.

Percent photolysis of cobalamin-fluorophore conjugate upon illumination at 546 nm (5 min), 646 nm (5 min), 700/727 nm (20 min) and 777 nm (10 min). Percent photolysis was calculated using the maximal observed fluorescent increase as 100% photolysis (see Figs S8, S10, S12, S14, S17, and S24).

Cobalamin
Conjugate
Fluorophore λab/ex (nm) [a] Percent Photolysis at Applied Wavelength (nm)

546 646 700/727[b] 777
Cbl-1 TAMRA 546 100 ± 17 [c] [c] [c]
Cbl-3 SulfoCy5 546, 646* 13 ± 21 100 ± 21 [c] [c]
Cbl-4 Atto725 546, 646, 727*, 777 62 ± 8 35 ± 5 100 ± 5 9 ± 5
Cbl-5 Dylight800 546, 727, 777* 22 ± 12 [c] 20 ± 12 100 ± 12
Cbl-6 Alexa700 546, 646, 700* 56 ± 3 48 ± 5 100 ± 3 [c]
Cbl-Bod Bodipy650 546, 646* 48 ±12 100 ± 12 [c] [c]
[a]

Absorbance/excitation of the cobalamin-fluorophore conjugate where * is the major fluorophore excitation band.

[b]

All compounds were photolyzed at 727 nm, except Cbl-6, which was photolyzed at 700 nm (3 min).

[c]

<5% photolyzed under the experimental conditions.