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. Author manuscript; available in PMC: 2018 Oct 1.
Published in final edited form as: Mol Oral Microbiol. 2017 Apr 18;32(5):375–389. doi: 10.1111/omi.12180

Fig. 7.

Fig. 7

The C-terminal region of Msp increases PIP3 lipid phosphatase activity. Neutrophils were pretreated with nMsp, rMsp, N, and C or truncated Msp followed by assessment of phosphate release from a synthetic PIP3 substrate using a malachite green assay. Neutrophils alone and neutrophils stimulate with fMLP were experimental controls. Results were compared to the control alone, with the C region causing the most phosphate release. Graph represents the mean ± SEM of 1 of 3 independent experiments all showing the same results (* P<0.05, ** P<0.01 unpaired t test).