Information for Peptide: HSQFLGYPITLYLEK from H90B2_HUMAN

1. Biological Peptide

1.1 Native Sequence

    K.HSQFLGYPITLYLEK.E

1.2 Peptide Properties

Start Stop MW m/z for 2+ m/z for 3+ pI
127 141 1807.95 904.98 603.66 6.75

1.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
H b y
S b y
Q b y
F b y
L b y
G b y
Y b y
P b y
I b y
T b y
L b y
Y b y
L b y
E b y
K b y

2. Synthetic Peptide

2.1 Synthetic (Internal Standard) Peptide Sequence

HSQFLGYPITLYL(C6N1)EK (Modification: Stable Isotope on L13 (U-13C6, 15N) )

2.2 Peptide Properties

MW m/z for 2+ m/z for 3+ pI
1814.97 908.49 606.0 6.75

2.3 Fragment Ion Table

AA b Ion Series b Ion Mass y Ion Series y Ion Mass
H b y
S b y
Q b y
F b y
L b y
G b y
Y b y
P b y
I b y
T b y
L b y
Y b y
L b y
E b y
K b y

2.4 Peptide Synthesis Report

Click to view/download synthesis report for HSQFLGYPITLYLEK

2.5 QqQ MS/MS

Transition Table:

Transition m/z of Transition Collision Energy
y3 396.26 34.0
y4 559.32 34.0
y5 672.4 34.0
y6 773.45 34.0
y7 886.51919 34.0
y8 983.57195 34.0
y9 1146.63528 34.0
y10 1203.65674 34.0
y11 1316.76 34.0
y12 1463.83 34.0

2.6 Calibration Curve of Standard

Description: NONE

 

Experiment Description: Cells from AML line U937 were lysed in 8M urea/ 100mM ammonium bicarbonate buffer on ice. The equivalent of 100,000 cells were 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