Table 2. Binding and penetrating activities of synthetic peptides in Beas-2B cells.
Peptide | Binding (%)a | Penetrating (%)b |
ECP32–41 | 100 | 100 |
EDN32–41 | 19.4±0.05*** | 17.0±4.24*** |
ECP32–41R3Q | 87.2±0.40 | 70.6±3.30* |
ECP32–41W4R | 549.9±1.00*** | 32.3±6.55** |
ECP33–41 | 54.7±3.37* | 48.2±2.48* |
ECP33–40 | 72.4±4.68* | 70.8±4.97* |
ECP34–41 | 39.3±2.76** | 34.3±2.41** |
ECP32–40 | 90.7±7.79 | 82.0±9.42 |
ECP32–39 | 82.6±3.20 | 35.0±6.98** |
ECP32–38 | 86.6±3.75 | 28.7±6.24** |
X: amino-n-butyric acid. ND: not determined. The result is expressed as the mean ± S.D., n = 4.
P<0.001;
P<0.01;
P<0.05.
Beas-2B cells were incubated with 5 µM FITC-peptides at 4°C for 1 h, washed twice with PBS, and subjected to ELISA. The amount of FITC-ECP32–41 bound to Beas-2B cells was normalized to 100%.
Beas-2B cells were incubated with 5 µM FITC-peptides at 37°C for 1 h. The cells were washed twice with 500 µl PBS, trypsinized at 37°C for 15 min, suspended in 500 µl PBS, and then subjected to flow cytometry. The fluorescence of cells treated with ECP32–41 was set as 100%.