To further study the roles of the two CheW proteins, a comparative bait fishing experiment was done (Figure 6). This experiment was performed as two-step bait fishing in which the second CheW was used as the control instead of plain CBD. CheW1 was bound to one cellulose column and incubated with light (12C) cell lysate. CheW2 was bound to a second column and incubated with heavy (13C) cell lysate. In this experiment,

the light forms (12C) of CheA and PurNH were present in high amounts whereas the heavy forms (13C) were hardly detectable (see Figure 6B for representative chromatograms of a CheA peptide). This demonstrates strong binding to CheW1 and no or only weak binding to CheW2. The membrane-bound Htrs identified in this experiment (Htr1, 2, 3, 4, 5, 6, 8, 14; i. e. all Htrs from group 1) exhibited a SILAC ratio of Talazoparib mouse nearly one, meaning they were bound to both CheWs to

the same extent. The three cytoplasmic transducers Htr11 (Car), Htr13 and Htr15 (group 3) were purified to a higher extent with CheW2 than with CheW1. Figure 6 Comparative bait fishing shows different interactions of the two CheW proteins. A Plot of the association score of proteins identified {Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|buy Anti-infection Compound Library|Anti-infection Compound Library ic50|Anti-infection Compound Library price|Anti-infection Compound Library cost|Anti-infection Compound Library solubility dmso|Anti-infection Compound Library purchase|Anti-infection Compound Library manufacturer|Anti-infection Compound Library research buy|Anti-infection Compound Library order|Anti-infection Compound Library mouse|Anti-infection Compound Library chemical structure|Anti-infection Compound Library mw|Anti-infection Compound Library molecular weight|Anti-infection Compound Library datasheet|Anti-infection Compound Library supplier|Anti-infection Compound Library in vitro|Anti-infection Compound Library cell line|Anti-infection Compound Library concentration|Anti-infection Compound Library nmr|Anti-infection Compound Library in vivo|Anti-infection Compound Library clinical trial|Anti-infection Compound Library cell assay|Anti-infection Compound Library screening|Anti-infection Compound Library high throughput|buy Antiinfection Compound Library|Antiinfection Compound Library ic50|Antiinfection Compound Library price|Antiinfection Compound Library cost|Antiinfection Compound Library solubility dmso|Antiinfection Compound Library purchase|Antiinfection Compound Library manufacturer|Antiinfection Compound Library research buy|Antiinfection Compound Library order|Antiinfection Compound Library chemical structure|Antiinfection Compound Library datasheet|Antiinfection Compound Library supplier|Antiinfection Compound Library in vitro|Antiinfection Compound Library cell line|Antiinfection Compound Library concentration|Antiinfection Compound Library clinical trial|Antiinfection Compound Library cell assay|Antiinfection Compound Library screening|Antiinfection Compound Library high throughput|Anti-infection Compound high throughput screening| in a comparative bait fishing experiment with both CheW proteins. Proteins bound to a higher extent to CheW2 than to CheW1 appear with a positive association score and proteins bound to higher extent to CheW1 than to CheW2 with a negative association score. Proteins bound to both baits to the same extent as well as background proteins appear with an association score close to 0. B Representative Methane monooxygenase extracted ion chromatograms of a peptide of CheA (N-terminal peptide MDDYLEAFVR). The upper panel shows the 13C form (fished by CheW2) and the lower panel the 12C form (fished by CheW1). These results are in www.selleckchem.com/products/fg-4592.html perfect agreement with the single bait fishing experiments and show the following: (1) both CheW proteins have a similar affinity to accessible group 1 Htrs when added exogenously. CheW2 has a higher affinity to group 3 Htrs

under these conditions; (2) CheW2 does not or only weakly binds CheA and forms complexes with Htrs to which CheA is not or only weakly bound; and (3) thus, under the tested conditions, only CheW1 is engaged in stable signaling complexes with CheA and Htrs. A possible interpretation is that CheW2 competes with CheW1 for binding to the Htrs and thereby impedes the formation of signaling complexes. Hence CheW2 in Hbt.salinarum could play a role similar to that of CheV in B.subtilis, which contains a CheW-like domain and a response regulator domain [103] and disrupts functional receptor-CheA coupling [48]. This could happen on a fast time scale in response to CheA activity, which would then be an adaptation system like CheV [48].