Hi,

I have a quick question about quantificaiton of SILAC samples using 13-
C6-Lysine as my heavy isotope.
I also tried reading through previous threads, and couldn't find a
direct answer to this question.

My questions:
(1) Does XPRESS support either fixed or variable modifications?
(2) I can see that ASAPRatio does, but I can't get that tool to work
properly.  What am I doing wrong?


FOR XPRESS ANALYSIS

Fixed Modifications:
Carbamidomethylation(C), Monoisotopic mass = 160.0306487

Variable Modifications:
Oxidized Methionine(M), Monoisotopic mass = 147.035
Pyroglutamic Acid(E), Monoisotopic mass = 112.0160439

I'm using 13-C6-Lysine as my heavy isotope, Monoisotopic mass =
134.115092

The settings I'm using in XPRESS:

Change XPRESS mass tolerance: 0.1
Change XPRESS residue mass difference: K, 6.02012902

How do I input the fixed and/or variable modifications listed above?

FOR ASAP RATIO ANALYSIS

Change labeled residues to: K
m/z range to include in summation of peak: 0.05
Specified residue mass 1: M, 147.035
Specified residue mass 2: C, 160.0306487
Specified residue mass 3: E, 112.0160439

Results:
(1) XPRESS quantifies a ratio of heavy/light and gives me a ratio,
however this analysis does not take into account any fixed or variable
modifications discussed above.
(2) ASAPRatio result is always "-1 +/- -1" and no chromatogram is
displayed when I click on that link.

Any ideas what I may be doing wrong?

Thank you VERY MUCH for your help,
Cyrus

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