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. 2014 Mar 12;9(3):e91007. doi: 10.1371/journal.pone.0091007

Table 1. Compilation of results.

cmc zeff Kins/105 Keff/108 Inline graphic MIC (L. lactis) MIC (E. coli) H5
MPX >1000 2.5±0.1 4.2±0.2 1.6±0.2 −24.0±0.3 2.5±0.5 8±3 18±2
Ala1 >1000 4.3±0.1 1.1±0.1 25±7 −18.4±0.3 18±7 33±8 230±10
Ala14 >1000 2.9±0.1 1.4±0.3 1.1±0.2 −16.2±0.3 21±4 33±8 220±20
PAMPX >1000 ----------- ----------- ----------- ----------- 3.3±0.8 21±4 25±1
Leu8 >1000 ----------- ----------- ----------- ----------- 2.5±1.3 7±3 14±2
Adec1 90±10 ----------- ----------- ----------- ----------- 1.7±0.4 3.3±0.8 0.7±0.1
Adec8 30±7 ----------- ----------- ----------- ----------- 4.2±0.8 4.2±0.8 1±1
Adec14 10±20 ----------- ----------- ----------- ----------- 1.7±0.4 3.3±0.8 0.8±0.2
OAMPX 150±50 ----------- ----------- ----------- ----------- 3.3±0.8 5±1 1.1±0.3

Critical micelle concentration (cmc in µM units), effective charge (zeff) of the peptide, partition coefficient of insertion (Kins), effective partition coefficient (Keff), molar enthalpy of partitioning (Inline graphic in kJ/mol units), minimal inhibitory concentration (MIC in µM units) and the haemolytic potency is given as the concentration H5 (in µM units) at which 5% haemolysis has been obtained. Membrane partitioning data for PAMPX, Leu8, Adec1, Adec8, Adec14 and OAMPX could not be analysed and these cells are marked with a dashed line.