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. 2013 Nov 6;8(11):e80043. doi: 10.1371/journal.pone.0080043

Figure 6. Selected N-terminal peptide derivatives synthesized from the second-phase diversification and quantification of their inhibitory activities against Plk1 PBD.

Figure 6

(A) Second-phase N-terminal-truncated PLHSpTM peptide derivatives generated using solid-phase peptide synthesis (SPPS) to study the binding nature of the pyrrolidine-binding region. (B) ELISA-based Plk1 PBD-binding IC50 graph (O.D., optical density). A representative graph from three independent experiments.