ppat.1006841.g006.tif (1.66 MB)
Binding of RbmC1 and RbmC2 to mammalian cells.
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posted on 2018-02-12, 18:46 authored by Swastik De, Katherine Kaus, Shada Sinclair, Brandon C. Case, Rich Olson(A) Fluorescence microscopy of defibrinated rabbit whole blood incubated with the RbmC2-GFPUV fusion. Wild-type or a D853A point mutation (with significantly reduced glycan-binding activity) are shown. Images include GFP, brightfield, and merged channels for constructs at 2.5 μM and 0.5 μM concentrations. Each WT/mutant pair was placed on an identical brightness scale, but WT and D853A are on different brightness scales. The white scale bar (lower right on the merged image) represents 10 microns. (B) Same as in A, but with WT RbmC1 and the D539A point mutation (purple asterisk on Fig 1C).
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cholerae secretes virulence factorscarboxy-terminal β- prism domaincholerae β- prism selectivitybind carbohydrate receptorsbiofilm proteins Vibrio choleraestrategybiofilm matrix proteinsRbmC β- prism domains targetpentasaccharide coreVCC β- prism domainRbmC β- prism domainVibrio cholerae cytolysintoxincholerae biofilm matrix protein RbmCβ- prism domainsglycantarget host cells
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