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. 2013 Jun 1;10(1):6. doi: 10.1186/1559-0275-10-6

Table 1.

Differentially expressed HCC, fibrotic liver nuclear membrane proteins and HepG2 cell line

Acc Name Abb Thr. pI; mass Score Peptide matched Cellular compartment PTM %age cov Mean normalized volume fibrosis HCC /HepG2 Ratio Anova (P) Fold change
 
 
 
 
 
 
CF(1), Membrane
 
 
 
 
 
 
 
P30049
ATP synthase subunit delta
ATPD
5.38; 17
58
5
mitochondrion
Isopeptide bond
17%
0.02536
0.00704
0.277
0.02
3.6
Mitochondrion
Ubl conjugation
 
 
 
 
 
 
inner membrane
 
 
 
 
 
 
 
P02675
Fibrinogen beta chain
FIBB
8.54; 55
1009
27
Secreted
Disulfide bond
41%
0.03364
0.01628
0.483
0.05
2.1
Glycoprotein
 
 
 
 
 
 
Pyrrolidone
 
 
 
 
 
 
carboxylic acid
 
 
 
 
 
 
P06576
ATP synthase subunit beta
ATPB
5.26; 56
670
18
CF(1), Membrane
Acetylation
29%
0.03448
0.00913
0.264
0.04
3.7
mitochondrion
Phosphoprotein
 
 
 
 
 
 
Mitochondrion inner membrane
 
 
 
 
 
 
 
Q549N7
Hemoglobin subunit beta
HBB
6.75;15
484
22
Heptoglobin-
Acetylation
61%
0.22697
0.11803
0.520
0.01
1.9
hemoglobin
Glycation
 
 
 
 
 
 
complex
Glycoprotein
 
Phosphoprotein
 
S-nitrosylation
P00167
Cytochrome b5 OS
CYB5A
4.88; 15
176
11
Cytoplasmic
Acetylation
42%
0.01948
0.05883
3.020
0.04
3.0
Endoplasmic
 
 
 
 
 
 
 
reticulum
Membrane
Microsome
P31930 Cytochrome b-c1 complex subunit 1 QCR1 5.94; 52 149 10 Mitochondrion
Acetylation
15%
0.01607
0.00505
0.314
0.05
3.1
inner membrane Phosphoprotein            

Accession no. is obtained from SWISS/Prot and percent coverage refers to the percentage of protein sequence coverage, determined by number of matched peptides. Significance was calculated from the Progenesis SameSpots v4.5 (Nonlinear Dynamic, UK), generated statistical analysis. A value of p < 0.05 was considered statistically significant. Functional classes were determined by searching the UniProt database (http://www.uniprot.org).

The proteins were separated on 2DE gels and identified by ESI-QTOF MS/MS.