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. 2018 Feb 16;9(12):3209–3214. doi: 10.1039/c7sc05407f

Fig. 1. (A and B) Time-dependent fluorescence spectra changes of POP (2 μM) upon treatment with Cys (100 equiv.) and GSH (10 equiv.), respectively, in PBS (10 mM, pH 7.4) at 37 °C. (C and D) Fluorescence intensity changes of POP (2 μM) treated with various amino acids (200 μM), reducing agents (200 μM), ROS (100 μM) and metal ions (500 μM). (1) POP; (2) His; (3) Glu; (4) Asp; (5) Val; (6) Phe; (7) Tyr; (8) Ala; (9) Ser; (10) Leu; (11) Arg; (12) Pro; (13) Thr; (14) Glu; (15) Trp; (16) Ile; (17) Lys; (18) DTT; (19) Vc; (20) HS for (C) and Cys for (D); (21) GSH for (C) and HS for (D); (22) ONOO; (23) H2O2; (24) NaOCl; (25)OH˙; (26) KO2; (27) NO; (28) HNO; (29) K+; (30) Ca2+; (31) Na+; (32) Mg2+; (33) Al3+; (34) Zn2+; (35) Cd2+; (36) Cu2+; (37) Fe2+; (38) Fe3+; (39) Cys for (C) and GSH for (D). For (A and C) λex = 450 nm; for (B and D) λex = 580 nm. Slits: 5/5 nm.

Fig. 1