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. 2013 Mar 4;8(3):e57318. doi: 10.1371/journal.pone.0057318

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.

a

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%.

b

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%.