How to extract residue information in case of line broadening (intensity drop ) of HSQC titration of protein - protein interaction data ?
 

How to extract residue information in case of line broadening (intensity drop ) of HSQC titration of protein - protein interaction data ?

Dear Friends

we have done HSQC gradient titration with targeted proteins , most of cross peaks we observed intensity drop , 30 out of 95 peaks ( 70 percent intensity drop of each cross peak ) , other cross peaks also we observe intensity drop less than 70 percent , we did n"t observe any chemical shift change .( May be it is due to intermediate exchange regime of complex ) .ITC experiment showing 12uM binding constant .AUC experiment result is complex size 33 kd .

is their any method to extract residue information from intensity drop of HSQC titration spectra more specifically ?

How to minimize line broadening effect while taking HSQC Titration ?



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