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. 2009 May 20;96(10):4299–4307. doi: 10.1016/j.bpj.2009.02.036

Table 2.

Comparison of time-resolved fluorometric parameters of DHE in lipid bilayers of different sterol mole fractions in the absence and presence of Aβ

Xsterol Aβ (μM) τ (ns) ρ (ns)
0.01 0 1.22 ± 0.01 7.30 ± 0.39
20m 1.10 ± 0.02 5.00 ± 0.22
20° 1.00 ± 0.01 6.87 ± 0.40
0.30 0 1.28 ± 0.01 10.58 ± 0.92
20m 1.46 ± 0.02 8.20 ± 0.55
20° 1.12 ± 0.01 12.24 ± 1.96
0.36 0 1.28 ± 0.01 10.27 ± 0.96
20m 1.50 ± 0.01 8.05 ± 0.57
20° 1.04 ± 0.01 12.72 ± 1.61
0.40 0 1.33 ± 0.01 11.30 ± 1.11
20m 1.54 ± 0.01 9.22 ± 0.69
20° 1.15 ± 0.01 15.25 ± 2.02
0.45 0 1.27 ± 0.02 10.21 ± 0.72
20m 1.52 ± 0.01 10.17 ± 0.65
20° 0.84 ± 0.02 10.27 ± 1.36

The average fluorescence decay lifetime (τ) and rotational correlation time (ρ) of DHE in the absence and presence of monomeric or oligomeric Aβ (denoted by superscript m or o, respectively) are shown.