Information for Peptide: IGTGSFGTVFR from ARAF_HUMAN

1. Biological Peptide

1.1 Native Sequence

    R.IGTGSFGTVFR.G

1.2 Peptide Properties

Start Stop MW m/z for 2+ m/z for 3+ pI
316 326 1140.59 571.3 381.21 9.75

1.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
I b y
G b y
T b y
G b y
S b y
F b y
G b y
T b y
V b y
F b y
R b y

2. Synthetic Peptide

2.1 Synthetic (Internal Standard) Peptide Sequence

IGTGSFGTVF(C9N1)R (Modification: Stable Isotope on F10 (13C, 15N) )

2.2 Peptide Properties

MW m/z for 2+ m/z for 3+ pI
1150.62 576.32 384.55 9.75

2.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
I b y
G b y
T b y
G b y
S b y
F b y
G b y
T b y
V b y
F b y
R b y

2.4 Peptide Synthesis Report

Click to view/download synthesis report for IGTGSFGTVFR

2.5 QqQ MS/MS

Transition Table:

Transition m/z of Transition Collision Energy
y10 1038.51656 23.0
y9 981.4951 23.0
y8 880.44742 22.0
y7 823.42596 25.0
y6 736.39393 24.0
y5 579.32551 24.0
y4 522.30405 23.0
y3 421.25637 29.0

2.6 Calibration Curve of Standard

Description: A dilution series was run from 50 fmol to 0.1 fmol. The detection limit was determined to be 10 fmol.

 

Experiment Description: Cells from the Melanoma cancer cell line were lysed in RIPA buffer. The equivalent of 200,000 cells were loaded onto an SDS gel. The protein of interest was excised and ingel digestion with trypsin was performed after reduction and alkylation with TCEP and IAA. 1/6 of the resulting digest was then analyzed on a Thermo Scientific TSQ mass spectrometer.

2.7 LC-MRM Analysis of Biological and Standard Peptides Illustrates Elution Times

2.8 Pseudo MS/MS Comparison of Transition Patterns for Biological/Standard Peptides