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. 2010 Dec 6;11(1):42–51. doi: 10.1002/pmic.201000273

Table 1.

Proteins identified by LC-MS as altered in response to LPS±minocycline pre-treatment

Protein spot number Accession number Uniprot recommended name (synonyms) Fold change (control versus LPS) Fold change (LPS versus minocycline + LPS) Fold change (control versus minocycline) p-Value Peptides identified % coverage
1 Unidentified 2.72 NS NS
2 Unidentified 4.08 NS NS
3 IPI00323357.3 Heat shock protein 71 Cognate (Heat shock protein 70 protein 8) 3.67 0.50 3.17 1.1×10−5 TVTNAVVTVPAYFNDSQR 8.03
DAGTIAGLNVLR
ARFEELNADLFR
FEELNADLFR
LLQDFFNGK
4 IPI00223757.3 Aldose reductase (Aldehyde reductase) 2.33 NS 2.98 1.8×10−8 TIGVSNFNPLQIER 4.46
5 IPI00468481.2 ATP Synthase β-subunit, mitochondrial NS 5.10 NS 1.7×10−6 FTQAGSEVSALLGR 2.55
6 IPI00468481.2 ATP synthase β-subunit, mitochondrial 3.15 NS NS 1.5×10−8 LVLEVAQHLGESTVR 9.81
LVDSGAPIKIPVGPETLGR
AIAELGIYPAVDPLDSTSR
7 Unidentified 0.33 2.26 NS
8 IPI00227299.5 Vimentin 0.24 2.90 NS 7.3×10−13 TYSLGSALRPSTSR 34.24
SLYSSSPGGAYVTR
LLQDSVDFSLADAINTEFK
FANYIDK
ILLAELELQLK
ILLAELELQLKGQGK
EEAESTLQSFRQDVDNASLAR
KVESLQEEIAFLK
KVESLQEEIAFLKK
FADLSEAANR
FADLSEAANRNNDALR
ISLPLPTFSSLNLR
ETNLESLPLVDTHSK
ETNLESLPLVDTHSKR
DGQVINETSQHHDDLE
9 IPI00338618.5 Probable phospholipid transporting ATPase VA (ATPase class V type 10A; P-locus fat-associated ATPase) 0.37 NS NS 4.7×10−5 FRGYIMHSNGEKAGLHK 1.15
10 IPI00462072.2 α-Enolase (2-phospho-D-glycerate hydrolyase; Non-neural enolase) 0.44 NS NS 1.9×10−5 YITPDQLADLYK 3.06
11 IPI00308885.5 Heat shock protein 60 (60 kDa chaperonin; Chaperonin 60) 0.27 3.98 NS 7.9×10−10 LVQDVANNTNEEAGDGTTTATVLAR 7.12
VGLQVVAVK
LSDGVALK
12 IPI0046841.2 ATP Synthase β-subunit, mitochondrial 0.32 NS NS 2.3×10−8 LVLEVAQHLGESSTVR 7.27
FTQAGSEVSALLGR
LVPLKETIK
13 Unidentified N/A Not detected in LPS treatment Not detected in control
14 IPI00353314.5 Olfactory Receptor Olfr 1204 N/A Not detected in LPS treatment Not detected in control 3.8×10−4 PAATLPIDKAVALFYTMITPMLNPLIYTLR 9.63

Summary of proteins identified by LC-MS analysis protein spots excised from two-dimension gels. Xcalibur 2.0 and Bioworks 3.1 software was used to identify proteins from LC-MS data. Fold change reported if statistically significantly altered (p<0.05), NS=not significant.