(A) Cells were treated with 100 µl of medium or PBS that was separately exposed to 1.55 J/cm2 plasma. (B) 100 µl of PBS, medium without serum, or PBS with 100 µg/ml BSA were treated with plasma (1.55 J/cm2) and immediately added to cells on a coverslip (separated, S). Cells overlaid with 100 µl of the indicated solution were treated with plasma (1.55 J/cm2) (direct, D). (C) Solutions containing the indicated amino acid (100 µM) were separately treated with plasma and then added to MCF10A cells. (A, B, C) After 1-minute incubation, cells on cover slips were diluted in 2 ml medium, followed by lysis and Western blot for γ-H2AX and α-tubulin. (D) Peroxidation efficiency of various amino acid components of cell culture medium when treated with IR [43]. For each amino acid, the amount of DNA damage induced is proportional to the peroxidation efficiency.