93 J/cm2). Photosensitisation of EMRSA-16 using the same conditions resulted in an approximate 4-log reduction in viability, showing that inactivation of this enzyme is effective within the parameters required to kill S. aureus in vitro. Figure 4 shows the effect of light dose on the activity of the V8 protease after exposure to laser light for 1, 2 and 5 minutes, corresponding to energy densities Enzalutamide nmr of 1.93 J/cm2, 3.86 J/cm2 and 9.65 J/cm2 respectively. Inactivation was also seen to be light dose-dependent and a 100% reduction in proteolytic

activity was achieved following 5 minutes AMG510 concentration irradiation with laser light in the presence of 20 μM methylene blue. Neither laser light nor methylene blue alone had an inhibitory effect on the activity of the V8 protease. SDS PAGE analysis (Figure 5) showed that after exposure to laser light and methylene blue, the bands derived from the V8 protease appeared to be progressively more smeared selleck chemicals llc and of lower intensity with increased irradiation time, demonstrating that photosensitisation may cause a change

in the protein, perhaps due to oxidation of the protein. A band of 29 kDa was expected for the V8 protease; however the gel showed some degradation of the V8 protease that could not be inhibited by the addition of a protease inhibitor. Figure 3 The effect of methylene blue dose and 1.93 J/cm 2 laser light on the proteolytic activity of V8 protease. An equal volume of either methylene blue (S+) (concentrations ranging from 1-20 μM) or PBS (S-) was added to V8 protease and samples were either exposed to laser light with an energy density of 1.93 J/cm2 (L+) (black bars) or kept in the dark (L-) (white bars). The activity of the V8 protease was assessed using the azocasein hydrolysis assay. Interleukin-2 receptor Error bars represent the standard deviation from the mean. *** P < 0.001 (ANOVA). Experiments were performed three times in triplicate and the combined

data are shown. Figure 4 The effect of 20 μM methylene blue and different laser light doses on the proteolytic activity of V8 protease. V8 protease was either kept in the dark (L-) or irradiated with laser light doses of 1.93 J/cm2, 3.86 J/cm2 and 9.65 J/cm2 (L+) in the presence of an equal volume of either PBS (S-) (white bars) or 20 μM methylene blue (S+) (black bars). Following irradiation, the activity of the enzyme was assessed using the azocasein hydrolysis assay. Error bars represent the standard deviation from the mean. *** P < 0.001 (ANOVA). Experiments were performed three times in triplicate and the combined data are shown. Figure 5 SDS PAGE analysis of V8 protease irradiated with methylene blue and laser light doses of 1.93 J/cm 2 , 3.86 J/cm 2 and 9.65 J/cm 2 . V8 protease was either kept in the dark (L-) or irradiated with laser light doses of 1.93 J/cm2, 3.86 J/cm2 and 9.