Information for Peptide: GSTAENAEYLR from EGFR_HUMAN

1. Biological Peptide

1.1 Native Sequence

    K.GSTAENAEYLR.V

1.2 Peptide Properties

Start Stop MW m/z for 2+ m/z for 3+ pI
1189 1199 1209.56 605.79 404.2 4.53

1.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
G b y
S b y
T b y
A b y
E b y
N b y
A b y
E b y
Y b y
L b y
R b y

2. Synthetic Peptide

2.1 Synthetic (Internal Standard) Peptide Sequence

ASTAENAEYLR (Modification: G1 to A )

2.2 Peptide Properties

MW m/z for 2+ m/z for 3+ pI
1223.58 612.8 408.87 4.53

2.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
A b y
S b y
T b y
A b y
E b y
N b y
A b y
E b y
Y b y
L b y
R b y

2.4 Peptide Synthesis Report

Click to view/download synthesis report for GSTAENAEYLR

2.5 QqQ MS/MS

Transition Table:

Transition m/z of Transition Collision Energy
y5 651.34664 24.0
y6 765.38957 24.0
y7 894.43216 24.0

2.6 Calibration Curve of Standard

Description: NONE

 

Experiment Description: Cells from Human Lung caner line HCC 827 were lysed in RIPA buffer on ice. 80ugs of the cell lysate was loaded onto a SDS gel. The protein of interest was excised and ingel digestion with trypsin was performed after reduction and alkylation with TCEP and IAA. 1/4 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

3. PTM Peptide

3.1 Native Sequence

    K.GSTAENAEyLR.V (PTM: Phosphorylation)

3.2 Peptide Properties

Start Stop MW m/z for 2+ m/z for 3+ pI
1189 1199 1289.53 645.77 430.85 4.53

3.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
G b y
S b y
T b y
A b y
E b y
N b y
A b y
E b y
y b y
L b y
R b y

4. Synthetic PTM Peptide

4.1 Synthetic (Internal Standard) Peptide Sequence

(NONE)

4.2 Peptide Properties

(NONE)

4.3 Fragment Ion Table

(NONE)

4.4 Peptide Synthesis Report

(NONE)

4.5 QqQ MS/MS

4.6 Calibration Curve of Standard

Description: NONE

 

Experiment Description: Cells from Human Lung caner line HCC 827 were lysed in RIPA buffer on ice. 80ugs of the cell lysate was loaded onto a SDS gel. The protein of interest was excised and ingel digestion with trypsin was performed after reduction and alkylation with TCEP and IAA. 1/4 of the resulting digest was then analyzed on a Thermo Scientific TSQ mass spectrometer.

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

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