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Table 3 Fold change of proteins that are differentially abundant in the synovial fluid of clinical non-responders compared with clinical responders to autologous chondrocyte implantation (ACI) immediately prior to stage II

From: Two independent proteomic approaches provide a comprehensive analysis of the synovial fluid proteome response to Autologous Chondrocyte Implantation

Protein

Fold Change

Identification method

Description

Accession

LF LC-MS/MS

iTRAQ nLC-MS/MS

40S Ribosomal protein S14

P62263

− 8.63

 

+

Kinectin

Q86UP2

− 6.20

 

+

Apolipoprotein C-III

P02656

− 2.78

 

+

High-mobility group protein B1

P09429

− 2.56

 

+

Kininogen-1

P01042

2.27

 

+

26S Protease regulatory subunit 7

P35998

2.34

+

 

26S Proteasome non-ATPase regulatory subunit 13

Q9UNM6

2.43

+

 

Alpha-enolase

P06733

2.56

 

+

Alpha-2-HS-glycoprotein

P02765

2.78

 

+

Hemopexin

P02790

2.88

 

+

Ferritin light chain

P02792

2.91

+

 

Platelet factor 4

P02776

3.26

+

 

Thrombospondin-1

P07996

3.40

+

 

Nucleosome assembly protein 1-like 1

P55209

4.94

+

 

Cofilin-1

P23528

7.08

+

 

EH domain-containing protein 1

Q9H4M9

7.30

+

 

Haemoglobin subunit delta

P02042

8.09

 

+

Protein S100-A6

P06703

8.39

 

+

T-complex protein 1 subunit eta

Q99832

8.43

+

 

Haemoglobin subunit beta

P68871

32.81

 

+

Haemoglobin subunit alpha

P69905

44.06

 

+

  1. Footnote: Differential abundance was denoted by greater than or equal to ± 2.0-fold change; p ≤ 0.05; protein identified by at least two unique peptides. Positive numbers denote higher abundance in non-responders than in responders. Proteins were identified using either protein dynamic compression coupled with label-free quantitation LC-MS/MS or no protein dynamic compression with isobaric tags for absolute and relative quantitation (iTRAQ) LC-MS/MS