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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Biochemistry. 2008 Aug 15;47(36):9540–9552. doi: 10.1021/bi800544d

Table 3.

Residues in RhoGDI-α Photolabeled by 3-Azioctanol and 3-Azibutanol Identified in Peptide Fragments Following Trypsinolysis and LTQ–FT Mass Spectrometry.

Agent [Alcohol]
µMa
AGGC Residue
Photolabeled
Peptideb Charge Rt, min Xcorr MH+c Accuracyd
ppm
3-azibutanol 100 + E193 [1] +3 23.45 5.29 2437.60 2.46
100 Photolabeled peptide not detected
3-azibutanol 100 + E163 [2] +2 22.52 5.06 1824.96 3.28
100 Photolabeled peptide not detected
3-azioctanol 10 + E163 [2] +2 18.82 2.95 1880.90 0.00
10 [2] +2 18.84 4.30 1880.90 0.00
Unlabeled peptide f E193 [1] +3 16.15 4.77 2365.54 0.00
E163 [2] +2 21.02 4.75 1752.89 0.00
a

Lowest 3-azialcohol concentration where photoincorporation was detected.

b

Peptides photolabeled by 3-azialcohols: [1]=RhoGDIα(181–199)=FTDDDKTDHLSWEWNLTIK; [2]= RhoGDIα(153–167)=AEEYEFLTPVEEAPK. Photolabeled residues are indicated in bold.

c

Representative observed masses which include increases due to photolabeling by 3-azioctanol (128 Dalton) or 3-azibutanol (72 Dalton).

e

Accuracy is the difference between the calculated and observed mass expressed in ppm.

f

Unlabeled peptides are those derived from that fraction of RhoGDIα which was not photolabeled during the experiment with 100 µM azibutanol in the presence of AGGC. See “EXPERIMENTAL PROCEDURES” section for other details