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. 2008 May 9;2:81–112.

Table 5.

Permeabilizing activity of WLIP and tolaasin I on vesicles of different lipid composition and a statistical analysis of their pore-formation mechanism.

Lipid Compositiona (mol%)
WLIP
Tolaasin I
PC SM sterol 1/C50b(μM−1) K1c (M−1) Md K2e 1/C50b (μM−1) K1c (M−1) Md K2e
100 0 0 0.59 ± 0.04 50 ± 20 8 ± 1 533 ± 451 2.8 ± 0.4 233 ± 52 6 ± 1 5.2 ± 2.6
50 50 0 1.41 ± 0.05 100 ± 30 6 ± 1 200 ± 340 4.9 ± 0.2 673 ± 179 6 ± 1 1.7 ± 1.1
50 33 16.5* 0.70 ± 0.05 100 ± 30 12 ± 1 217 ± 247 2.8 ± 0.2 200 ± 50 6 ± 1 12 ± 12
50 16.5 33* 0.59 ± 0.01 50 ± 20 8 ± 1 533 ± 451 1.2 ± 0.2 100 ± 30 7 ± 1 19.7 ± 17.4
50 0 50* 0.45 ± 0.01 50 ± 20 11 ± 1 533 ± 451 0.4 ± 0.1 50 ± 20 7 ± 1 0.8 ± 0.3
50 33 16.5§ 0.70 ± 0.03 100 ± 30 12 ± 1 413 ± 440 2.5 ± 0.2 250 ± 54 7 ± 1 2.8 ± 1.7
50 16.5 33§ 0.59 ± 0.08 50 ± 20 8 ± 1 533 ± 451 1.3 ± 0.1 100 ± 30 7 ± 1 30 ± 20
50 0 50§ 0.54 ± 0.01 50 ± 20 10 ± 1 533 ± 451 1.0 ± 0.2 50 ± 20 5 ± 1 30 ± 20
a

Lipid mixtures are reported on a molar base. PC: egg phosphatidylcholine; SM: sphyngomyelin; the sterol included in the vesicles was cholesterol* and ergosterol§.

b

The permeabilising activity is expressed as the reciprocal of the concentration of toxin causing 50% of calcein release (C50). Data are average ± S.D. of at least two different experiments.

c

The partition coefficient of toxin monomers into the liposome.

d

The number of monomers necessary for the formation of an active pore.

e

The aggregation process of membrane-inserted monomers.

c; d ; e

Data are average ± S.D. of at least three different experiments.