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. 2018 Mar 9;8:4305. doi: 10.1038/s41598-018-22364-z

Figure 2.

Figure 2

B49Mod1 completely retains the anti-adhesion function of B49 without affecting cell viability. (A) Cartoon depiction a BST-2-targeting peptide (B49) and a smaller B49 analog that lacks penetratin at the N-terminus (B49Mod1) and is more stable as defined by half-life in silico analyses. (B,C) Cellular viability of several (B) human and (C) mouse breast cancer cell lines following a 24-hour treatment with vehicle (1:8 (v/v) acetonitrile:water) or with 200 ng/well of B49Mod1. (D) Adherence of E0771 shControl (shCTL) cells to E0771 shControl monolayers that were pre-treated with Vehicle, B49, or B49Mod1 for 4 hours at 200 ng/well before addition of incoming cells. (E,F) Adherence of PKH67-labeled E0771 shControl or shBST-2 cells to E0771 shControl monolayers that were pre-treated with (E) B49Mod1 at 200 ng/well or (F) with an equivalent volume of Vehicle for 4 hours. (G,H) Adherence of 4T1 (G) shControl or (H) shBST-2 cells to 4T1 shControl monolayers that were pre-treated with Vehicle (green) or B49Mod1 (gray) at 200 ng/well for 4 hours. (I,J) Adherence of 4T1 (I) shControl or (J) shBST-2 cells to 4T1 shBST-2 monolayers that were pre-treated with Vehicle (green) or B49Mod1 (gray) at 200 ng/well for 4 hours. Error bars correspond to SEM. Significance was taken at *P < 0.05, **P < 0.01 and ***P < 0.001. ns = not significant.