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. 2020 Jan 2;28:105067. doi: 10.1016/j.dib.2019.105067

Dataset on the mass spectrometry-based proteomic profiling of the kidney from wild type and the dystrophic mdx-4cv mouse model of X-linked muscular dystrophy

Paul Dowling a,b, Margit Zweyer c, Maren Raucamp c, Michael Henry d, Paula Meleady d, Dieter Swandulla c, Kay Ohlendieck a,b,
PMCID: PMC6956748  PMID: 31956673

Abstract

The proteomic data presented in this article provide supporting information to the related research article “Proteomic and cell biological profiling of the renal phenotype of the mdx-4cv mouse model of Duchenne muscular dystrophy” (Dowling et al., 2019) [1]. This article supplies additional datasets on protein species with increased versus decreased concentration in the kidney from the dystrophic mdx-4cv mouse, as well as tables with mass spectrometrically identified kidney marker proteins that exhibit characteristic tissue distributions, subcellular localizations and physiological functions. Information is provided on the underlying multi-consensus protein listings from the proteomic screening of both wild type and mdx-4cv mouse kidneys. The data article provides comprehensive information on the systematic and mass spectrometric identification of the mouse kidney proteome.

Keywords: Kidney proteome, Mass spectrometry, Muscular dystrophy, Proteomics


Specifications Table

Subject Biochemistry
Specific subject area Biomedicine
Type of data Tables
How data were acquired LC-MS/MS analysis, using an Orbitrap Fusion Tribrid Mass Spectrometer (Thermo Scientific)
Data format Raw data and analysed data
Parameters for data collection Renal protein was extracted from whole kidneys from wild type and dystrophic mdx-4cv mice.
Description of data collection Comparative mass spectrometry-based proteomic profiling of kidney extracts
Data source location Maynooth, Co. Kildare, Ireland
Data accessibility The data on kidney marker proteins are available with this article.
The multi-consensus file and raw data files of all identified kidney proteins is available through a public repository.
Repository name: Open Science Framework
Data identification number: bz3kv
Direct URL to data: https://osf.io/bz3kv/
Related research article Paul Dowling, Margit Zweyer, Maren Raucamp, Michael Henry, Paula Meleady, Dieter Swandulla and Kay Ohlendieck
Proteomic and cell biological profiling of the renal phenotype of the mdx-4cv mouse model of Duchenne muscular dystrophy
European Journal of Cell Biology (2019)
(available online November 18, 2019, 151059) https://doi.org/10.1016/j.ejcb.2019.151059
Value of the Data
  • Mass spectrometric data presented in this article provide a detailed listing of the protein isoforms of the assessable mouse kidney proteome.

  • Proteomic data provide a summary of changed renal proteins in the dystrophic mdx-4cv mouse model of X-linked muscular dystrophy.

  • The proteomic data give an overview of the identification of tissue-specific kidney marker proteins.

  • The mass spectrometric data are valuable to serve as a comprehensive repository of the mouse proteome for comparative biochemical studies.

1. Data

This data paper presents the findings from the mass spectrometric profiling of mouse kidney extracts, and relates to the comparative survey of the renal proteome from wild type versus the dystrophic mdx-4cv mouse model of Duchenne muscular dystrophy [1]. With the help of an Orbitrap Fusion Tribrid mass spectrometer, 5878 protein species were identified in renal tissue extracts. The multi-consensus file of mouse kidney that contains data from the analysis of 28 separate mass spectrometric sample runs, as well as the raw data underlying the cataloguing of the kidney, has been deposited to the Open Science Framework under the project title ‘Proteomic profiling of mouse kidney’; Link: https://osf.io/bz3kv/(Date created: 2018-10-04; Date made public: 2019-12-02). The analyses were carried out with 2 technical repeats of 7 biological repeats of 12-month old wild type kidney extracts, as well as 2 technical repeats of 7 biological repeats of 12-month old mdx-4cv kidney extracts. In relation to the report by Dowling et al. [1], additional datasets on proteins with an increased versus decreased concentration in the kidney from the dystrophic mdx-4cv mouse are presented in Table 1, Table 2. Table 1 lists the mass spectrometric identification of kidney proteins with a less than 1.5-fold increase in the mdx-4cv mouse. Kidney proteins with a less than 1.5-fold increased concentration in the mdx-4cv mouse are presented in Table 2. The most abundant high-molecular-mass kidney proteins are presented in Table 3. Information on typical tissue-specific kidney marker proteins [[2], [3], [4], [5], [6]] is provided in Table 4. In Table 5 are listed mass spectrometrically identified kidney marker proteins with characteristic physiological functions in ion homeostasis, including specific isoforms of the sodium/calcium exchanger, sodium/glucose cotransporter, the plasma membrane calcium-transporting ATPase, the sodium/potassium-transporting ATPase, the endoplasmic reticulum calcium ATPase, calcium-binding proteins, voltage-dependent calcium channels and chloride channels [2]. In relation to the comparative survey of fatty acid binding proteins in the kidney from wild type versus the dystrophic mdx-4cv mouse model of dystrophinopathy [1], Table 6 lists the fatty acid binding proteins that were identified by mass spectrometry. This includes fatty acid-binding protein isoforms FABP1, FABP3, FABP4, FABP5 and FABP7 [7]. Kidney dystrophin and its associated proteins were identified in renal extracts, including dystrophin (Dp140), dystroglycan, alpha-1-syntrophin, beta-2-syntrophin, epsilon-sarcoglycan, alpha-dystrobrevin and beta-dystrobrevin [8], as listed in Table 7.

Table 1.

Proteomic identification of kidney proteins with an increased abundance below 1.5-fold in the mdx-4cv model of Duchenne muscular dystrophy.

Accession Protein Gene Unique peptides Confidence score Anova (p) Max fold change
O35657 Sialidase-1 Neu1 2 4.6649 0.00419 1.49
O54990 Prominin-1 Prom1 2 13.8091 0.01535 1.49
Q91WU2 Solute carrier family 22 member 7 Slc22a7 2 5.6395 0.04080 1.49
D3Z7P3 Glutaminase kidney isoform, mitochondrial Gls 3 12.9045 0.00653 1.48
P48758 Carbonyl reductase [NADPH] 1 Cbr1 4 17.5670 0.00074 1.48
Q61391 Neprilysin Mme 4 12.3698 0.00261 1.48
G5E829 Plasma membrane calcium-transporting ATPase 1 Atp2b1 2 7.9881 0.00011 1.47
P24472 Glutathione S-transferase A4 Gsta4 2 5.6183 0.00201 1.47
O88343 Electrogenic sodium bicarbonate cotransporter 1 Slc4a4 7 22.6034 1.04E-08 1.47
Q9R257 Heme-binding protein 1 Hebp1 2 8.7884 0.00369 1.46
P61922 4-aminobutyrate aminotransferase, mitochondrial Abat 6 21.809 4.63E-05 1.46
O70370 Cathepsin S Ctss 2 9.0446 0.00011 1.45
P70172 Ileal sodium/bile acid cotransporter Slc10a2 2 5.4973 0.00038 1.45
P24452 Macrophage-capping protein Capg 2 5.5246 0.02331 1.45
P97449 Aminopeptidase N Anpep 5 27.1718 0.00188 1.45
Q8BMS1 Trifunctional enzyme subunit alpha, mitochondrial Hadha 2 6.4455 0.00174 1.44
Q9QXE0 2-hydroxyacyl-CoA lyase 1 Hacl1 2 9.9044 0.00925 1.44
Q9D687 Sodium-dependent neutral amino acid transporter B(0)AT1 Slc6a19 3 10.4909 1.27E-06 1.43
Q9D964 Glycine amidinotransferase, mitochondrial Gatm 2 7.0537 0.00819 1.42
Q9Z306 Solute carrier family 22 member 4 Slc22a4 2 6.6313 0.00929 1.42
Q49B93 Sodium-coupled monocarboxylate transporter 2 Slc5a12 2 6.7141 1.69E-05 1.41
Q9CQ65 S-methyl-5′-thioadenosine phosphorylase Mtap 2 5.9308 0.00323 1.41
P23780 Beta-galactosidase Glb1 2 6.2503 0.00437 1.4
P24668 Cation-dependent mannose-6-phosphate receptor M6pr 2 6.5894 0.04069 1.4
P09470 Angiotensin-converting enzyme Ace 12 42.5194 0.00642 1.4
Q8VCZ9 Hydroxyproline dehydrogenase Prodh2 2 6.1044 0.00172 1.39
P45376 Aldose reductase Akr1b1 5 13.6831 0.00165 1.39
O88986 2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial Gcat 3 10.1459 4.10E-05 1.38
Q9WV92 Band 4.1-like protein 3 Epb41l3 4 14.7070 0.00046 1.38
Q9DBT9 Dimethylglycine dehydrogenase, mitochondrial Dmgdh 5 18.8616 0.00028 1.38
O88428 Bifunctional 3′-phosphoadenosine 5′-phosphosulfate synthase 2 Papss2 11 37.6264 0.00095 1.38
O09164 Extracellular superoxide dismutase [Cu–Zn] Sod3 2 11.3667 1.53E-05 1.37
O70493 Sorting nexin-12 Snx12 4 10.9785 6.57E-06 1.36
Q9Z1G3 V-type proton ATPase subunit C 1 Atp6v1c1 4 14.1960 0.00010 1.36
Q9R092 17-beta-hydroxysteroid dehydrogenase type 6 Hsd17b6 2 7.8166 0.00030 1.35
Q9EQ20 Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial Aldh6a1 2 7.8288 0.02301 1.35
Q8K157 Aldose 1-epimerase Galm 3 10.5439 0.00726 1.35
P16406 Glutamyl aminopeptidase Enpep 10 35.0875 1.14E-06 1.35
Q9QWR8 Alpha-N-acetylgalactosaminidase Naga 3 8.1744 0.00102 1.34
Q9DCJ9 N-acetylneuraminate lyase Npl 4 13.4008 0.00150 1.34
Q8R3P0 Aspartoacylase Aspa 2 4.8961 5.94E-05 1.33
P24527 Leukotriene A-4 hydrolase Lta4h 2 7.3695 0.00689 1.33
P16675 Lysosomal protective protein Ctsa 2 7.8468 0.01961 1.33
Q00519 Xanthine dehydrogenase/oxidase Xdh 3 11.0764 0.00741 1.33
P10649 Glutathione S-transferase Mu 1 Gstm1 4 16.5436 6.74E-05 1.33
Q91X52 l-xylulose reductase Dcxr 5 22.2456 5.55E-07 1.33
P50431 Serine hydroxymethyltransferase, cytosolic Shmt1 6 19.5642 0.00172 1.33
Q9CXN7 Phenazine biosynthesis-like domain-containing protein 2 Pbld2 3 13.0305 5.80E-07 1.32
P15626 Glutathione S-transferase Mu 2 Gstm2 3 10.7236 0.00011 1.32
Q99LB7 Sarcosine dehydrogenase, mitochondrial Sardh 4 14.0763 6.64E-05 1.32
Q99MZ6 Unconventional myosin-VIIb Myo7b 4 11.6505 0.00061 1.32
Q91Y97 Fructose-bisphosphate aldolase B Aldob 5 22.2473 0.02101 1.32
P26443 Glutamate dehydrogenase 1, mitochondrial Glud1 6 19.3021 2.20E-07 1.32
P48774 Glutathione S-transferase Mu 5 Gstm5 3 8.9950 3.80E-05 1.31
O88844 Isocitrate dehydrogenase [NADP] cytoplasmic Idh1 3 8.7557 0.00071 1.31
Q62433 Protein NDRG1 Ndrg1 5 23.1403 1.78E-05 1.31
Q91VA0 Acyl-coenzyme A synthetase ACSM1, mitochondrial Acsm1 5 19.1532 0.00374 1.31
P10493 Nidogen-1 Nid1 2 8.7788 0.00333 1.3
O70404 Vesicle-associated membrane protein 8 Vamp8 2 6.0734 0.00493 1.3
Q61739 Integrin alpha-6 Itga6 3 11.8001 0.00020 1.3
P01027 Complement C3 C3 3 9.6830 0.00063 1.3
A2ARV4 Low-density lipoprotein receptor-related protein 2 Lrp2 5 22.3161 0.00409 1.3
P12382 ATP-dependent 6-phosphofructokinase, liver type Pfkl 3 12.7193 0.00370 1.29
P11881 Inositol 1,4,5-trisphosphate receptor type 1 Itpr1 5 17.8101 3.12E-05 1.29
P28271 Cytoplasmic aconitate hydratase Aco1 2 4.3600 0.00364 1.28
Q8VCT4 Carboxylesterase 1D Ces1d 2 6.6092 0.01551 1.28
Q91YI0 Argininosuccinate lyase Asl 2 8.7531 0.00032 1.27
Q64471 Glutathione S-transferase theta-1 Gstt1 2 5.5587 0.00013 1.26
Q6P1B1 Xaa-Pro aminopeptidase 1 Xpnpep1 3 7.8825 0.03278 1.26
P10852 4F2 cell-surface antigen heavy chain Slc3a2 4 10.4098 0.00265 1.26
Q9WVK4 EH domain-containing protein 1 Ehd1 2 5.8015 0.00026 1.25
Q71LX4 Talin-2 Tln2 2 6.9617 0.01162 1.25
Q8VC30 Triokinase/FMN cyclase Tkfc 3 10.8554 0.00073 1.25
P06281 Renin-1 Ren1 4 10.7058 0.00451 1.25
P63158 High mobility group protein B1 Hmgb1 2 6.2009 3.14E-05 1.24
Q9D0F9 Phosphoglucomutase-1 Pgm1 2 5.4388 0.00027 1.24
O88909 Solute carrier family 22 member 8 Slc22a8 3 9.1520 5.17E-06 1.24
Q3U4I7 Pyridine nucleotide-disulfide oxidoreductase domain-containing protein 2 Pyroxd2 3 10.0392 0.00151 1.24
Q9NYQ2 Hydroxyacid oxidase Hao2 3 11.4539 0.02747 1.24
O70475 UDP-glucose 6-dehydrogenase Ugdh 5 19.0586 0.00356 1.24
Q8BUV3 Gephyrin Gphn 2 6.3220 0.00830 1.22
Q99K51 Plastin-3 Pls3 2 6.6408 0.01267 1.21
Q9DBM2 Peroxisomal bifunctional enzyme Ehhadh 2 8.7039 0.01977 1.21
Q9Z1N5 Spliceosome RNA helicase Ddx39b Ddx39b 2 6.8126 0.02905 1.21
Q8R0N6 Hydroxyacid-oxoacid transhydrogenase, mitochondrial Adhfe1 3 10.8822 5.79E-06 1.21
P16546 Spectrin alpha chain, non-erythrocytic 1 Sptan1 3 11.5102 0.00302 1.21
Q99JY0 Trifunctional enzyme subunit beta, mitochondrial Hadhb 4 13.9444 0.00113 1.2

Table 2.

Proteomic identification of kidney proteins with a decreased abundance below 1.5-fold in the mdx-4cv model of Duchenne muscular dystrophy.

Accession Protein Gene Unique peptides Confidence score Anova (p) Max fold change
P48024 Eukaryotic translation initiation factor 1 Eif1 2 8.4814 0.00013 1.49
Q9JHR7 Insulin-degrading enzyme Ide 2 5.2327 0.04111 1.46
P11862 Growth arrest-specific protein 2 Gas2 3 9.2866 4.11E-05 1.46
Q9DBG6 Dolichyl-diphospho-oligosaccharide-protein glycosyltransferase subunit 2 Rpn2 2 8.4270 0.00186 1.45
Q61838 Pregnancy zone protein Pzp 9 29.2658 0.00065 1.42
Q61847 Meprin A subunit beta Mep1b 2 7.1821 0.00095 1.4
P12658 Calbindin Calb1 2 5.1746 0.01903 1.4
Q9CPY7 Cytosol aminopeptidase Lap3 3 10.4237 0.02227 1.4
Q9DCY0 Glycine N-acyltransferase-like protein Keg1 Keg1 2 4.7402 0.00128 1.39
Q9CR67 Transmembrane protein 33 Tmem33 2 6.1302 0.00735 1.38
Q61207 Prosaposin Psap 2 5.1656 0.00022 1.37
Q8JZZ0 UDP-glucuronosyltransferase 3A2 Ugt3a2 2 6.4221 0.02672 1.37
Q9DBX3 Sushi domain-containing protein 2 Susd2 4 14.5368 0.00470 1.37
Q9Z1J3 Cysteine desulfurase, mitochondrial Nfs1 2 11.6958 1.28E-05 1.36
Q3U9G9 Lamin-B receptor Lbr 2 7.4723 0.00013 1.36
Q9CQH7 Transcription factor BTF3 homolog 4 Btf3l4 2 8.2813 3.81E-05 1.34
Q9CYH2 Redox-regulatory protein FAM213A Fam213a 2 6.9334 0.00034 1.34
Q05920 Pyruvate carboxylase, mitochondrial Pc 2 5.6710 0.00120 1.32
Q05793 Basement membrane-specific heparan sulfate proteoglycan core protein Hspg2 2 5.5448 0.00348 1.32
P12970 60S ribosomal protein L7a Rpl7a 2 6.4383 0.01017 1.32
P51885 Lumican Lum 2 7.6116 0.02121 1.32
Q00915 Retinol-binding protein 1 Rbp1 2 6.9546 0.00513 1.31
Q8BFW7 Lipoma-preferred partner homolog Lpp 2 5.7683 0.01836 1.31
Q8QZT1 Acetyl-CoA acetyltransferase, mitochondrial Acat1 2 8.9227 0.00886 1.3
O08638 Myosin-11 Myh11 13 44.8107 5.02E-05 1.3
P21107 Tropomyosin alpha-3 chain Tpm3 2 7.0891 2.93E-05 1.29
Q99JB2 Stomatin-like protein 2, mitochondrial Stoml2 2 7.7193 4.81E-05 1.29
Q32MW3 Acyl-coenzyme A thioesterase 10, mitochondrial Acot10 3 11.9828 0.00043 1.28
P58774 Tropomyosin beta chain Tpm2 2 7.4480 0.00049 1.27
P37804 Transgelin Tagln 2 5.2768 0.01312 1.27
P21271 Unconventional myosin-Vb Myo5b 2 6.2358 0.02245 1.27
P09103 Protein disulfide-isomerase P4hb 2 5.3654 0.03115 1.27
Q9CR98 Protein FAM136A Fam136a 2 5.8057 0.00522 1.26
P28653 Biglycan Bgn 2 7.9254 0.00548 1.26
Q8BHN3 Neutral alpha-glucosidase AB Ganab 3 8.1991 0.00178 1.26
Q02257 Junction plakoglobin Jup 2 7.6926 0.01217 1.25
Q9D7X8 Gamma-glutamylcyclo-transferase Ggct 2 7.4681 0.01870 1.25
Q8BJ64 Choline dehydrogenase, mitochondrial Chdh 4 9.5358 0.00213 1.25
Q8CC88 von Willebrand factor A domain-containing protein 8 Vwa8 8 30.5625 0.01240 1.24
Q80X90 Filamin-B Flnb 18 64.3416 0.00358 1.24
P51174 Long-chain specific acyl-CoA dehydrogenase, mitochondrial Acadl 2 5.1602 0.00186 1.23
Q78IK4 MICOS complex subunit Mic27 Apool 2 5.9301 3.43E-06 1.22
Q06770 Corticosteroid-binding globulin Serpina6 2 7.0902 0.00323 1.22
Q7TPR4 Alpha-actinin-1 Actn1 2 5.6749 0.00332 1.22
Q91X72 Hemopexin Hpx 2 4.4037 0.03030 1.22
Q8QZY2 Glycerate kinase Glyctk 3 12.7538 0.00018 1.22
Q61543 Golgi apparatus protein 1 Glg1 3 12.1393 0.00718 1.21
Q3V3R4 Integrin alpha-1 Itga1 4 11.2984 0.00068 1.21
Q8VDD5 Myosin-9 Myh9 15 57.2338 0.00070 1.21
Q8BL66 Early endosome antigen 1 Eea1 3 13.5801 5.59E-05 1.2
Q64727 Vinculin Vcl 6 20.2663 0.00409 1.2

Table 3.

List of mass spectrometrically identified high-molecular-mass mouse kidney proteins that are covered by a large number of unique peptide sequences.

Accession Protein name Gene Peptides Unique peptides Coverage (%) Molecular mass (kDa)
A2ARV4 Low-density lipoprotein receptor-related protein 2 Lrp2 187 187 56 518.9
P16546 Spectrin alpha chain, non-erythrocytic 1 Sptan1 158 158 72 284.4
Q62261 Spectrin beta chain, non-erythrocytic 1 Sptbn1 143 137 70 274.1
Q8VDD5 Myosin-9 Myh9 125 103 64 226.2
Q9JHU4 Cytoplasmic dynein 1 heavy chain 1 Dync1h1 184 184 50 531.7
Q9QXS1 Plectin Plec 119 119 30 533.9
Q80X90 Filamin-B Flnb 116 108 65 277.7
Q8BTM8 Filamin-A Flna 108 99 60 281
P26039 Talin-1 Tln1 107 94 65 269.7
Q05793 Basement membrane-specific heparan sulfate proteoglycan core protein Hspg2 103 103 46 398
Q9QXZ0 Microtubule-actin cross-linking factor 1 Macf1 99 97 19 831.4
Q68FD5 Clathrin heavy chain 1 Cltc 90 90 74 191.4
Q9JLB4 Cubilin Cubilin 83 83 34 398.8
Q61001 Laminin subunit alpha-5 Lama5 84 84 38 403.8
O08638 Myosin-11 Myh11 89 68 50 226.9
Q61879 Myosin-10 Myh10 90 68 50 228.9
Q8CC88 von Willebrand factor A domain-containing protein 8 Vwa8 88 88 61 213.3
Q71LX4 Talin-2 Tln2 81 68 51 253.5

Table 4.

List of mass spectrometrically identified mouse kidney marker proteins with a characteristic cellular localization.

Accession Protein name Gene Coverage (%) Unique peptides Cellular localization
Q91X05 Podocin Nphs2 18 4 Glomeruli podocytes
Q9QZS7 Nephrin Nphs1 7 5 Glomeruli
P61148 Fibroblast growth factor FGF1 Fgf1 33 5 Glomeruli
Q9QXN5 Inositol oxygenase Miox 74 12 Proximal tubule cytoplasm
O70577 Solute carrier family 22 member 2 Slc22a2 10 4 Proximal tubule basolateral membrane
O88909 Solute carrier family 22 member 8 Slc22a8 20 10 Proximal tubule basolateral membrane
Q60825 Sodium-dependent phosphate transport protein 2A Slc34a1 28 12 Proximal tubule luminal membrane
Q8CFZ5 Solute carrier family 22 member 12 Slc22a12 19 12 Proximal tubule luminal membrane
O88576 Sodium-dependent neutral amino acid transporter B(0)AT3 Slc6a18 14 7 Proximal tubule luminal membrane
Q6A4L0 Solute carrier family 22 member 13 Slc22a13 12 6 Proximal tubule luminal membrane
Q91X17 Uromodulin Umod 33 18 Distal tubule cytoplasm
O88335 ATP-sensitive inward rectifier potassium channel 1 Kcnj1 10 3 Distal tubule luminal membrane
P55014 Solute carrier family 12 member 1 Slc12a1 40 32 Distal tubule luminal membrane
P59158 Solute carrier family 12 member 3 Slc12a3 29 20 Distal tubule luminal membrane
P56402 Aquaporin-2 Aqp2 13 3 Collecting duct luminal membrane

Table 5.

List of mass spectrometrically identified mouse kidney marker proteins with characteristic physiological functions in ion homeostasis.

Accession Protein name Gene Coverage (%) Peptides Unique Peptides Molecular mass [kDa]
P70414 Sodium/calcium exchanger 1 Slc8a1 6 5 5 108
Q8K596 Sodium/calcium exchanger 2 Slc8a2 4 2 1 100.6
Q8C3K6 Sodium/glucose cotransporter 1 Slc5a1 22 13 13 73.4
Q923I7 Sodium/glucose cotransporter 2 Slc5a2 16 10 9 73
Q8VDT1 Sodium/glucose cotransporter 4 Slc5a9 18 8 7 75
Q5SWY8 Sodium/glucose cotransporter 5 Slc5a10 20 8 8 64.7
G5E829 Plasma membrane calcium-transporting ATPase 1 Atp2b1 30 27 17 134.7
Q6Q477 Plasma membrane calcium-transporting ATPase 4 Atp2b4 25 22 12 133
Q8VDN2 Sodium/potassium-transporting ATPase subunit alpha-1 Atp1a1 50 47 31 112.9
Q6PIE5 Sodium/potassium-transporting ATPase subunit alpha-2 Atp1a2 21 17 1 112.1
Q6PIC6 Sodium/potassium-transporting ATPase subunit alpha-3 Atp1a3 24 17 2 111.6
P14094 Sodium/potassium-transporting ATPase subunit beta-1 Atp1b1 52 15 15 35.2
P97370 Sodium/potassium-transporting ATPase subunit beta-3 Atp1b3 19 4 4 31.8
O55143 Sarcoplasmic/endoplasmic reticulum calcium ATPase 2 Atp2a2 46 43 36 104.4
Q64518 Sarcoplasmic/endoplasmic reticulum calcium ATPase 3 Atp2a3 16 14 7 103.8
Q80XR2 Calcium-transporting ATPase type 2C member 1 Atp2c1 10 6 6 91.8
Q06138 Calcium-binding protein 39 Cab39 40 14 10 34.1
Q64374 Regucalcin Rgn 33 8 8 29.9
P0DP27 Calmodulin-2 Calm2 72 10 10 14.9
Q9DB16 Calcium-binding protein 39-like Cab39l 28 10 6 33.7
P12658 Calbindin Calb1 67 20 20 30
P97816 Protein S100-G S100g 71 8 8 9
P14211 Calreticulin Calr 68 19 19 48
O08532 Voltage-dependent calcium channel subunit alpha-2/delta-1 Cacna2d1 17 14 14 110.3
Q02789 Voltage-dependent L-type calcium channel subunit alpha-1S Cacna1s 1 1 1 188.0
Q921L3 Calcium load-activated calcium channel Tmco1 12 2 2 21.2
Q60932 Voltage-dependent anion-selective channel protein 1 Vdac1 73 18 17 32.3
Q60930 Voltage-dependent anion-selective channel protein 2 Vdac2 57 11 11 31.7
Q60931 Voltage-dependent anion-selective channel protein 3 Vdac3 52 10 9 30.7
Q9EPK8 Transient receptor potential cation channel subfamily V member 4 Trpv4 15 9 9 98
O88335 ATP-sensitive inward rectifier potassium channel 1 Kcnj1 10 3 3 42.7
O88932 ATP-sensitive inward rectifier potassium channel 15 Kcnj15 6 3 3 42.6
Q9Z307 Inward rectifier potassium channel 16 Kcnj16 9 4 4 48
Q9WUB7 Chloride channel protein ClC-Ka Clcnka 11 6 4 68.7
Q9WUB6 Chloride channel protein ClC-Kb Clcnkb 13 6 4 68.7
Q99LI2 Chloride channel CLIC-like protein 1 Clcc1 12 4 4 53.9
Q9Z1Q5 Chloride intracellular channel protein 1 Clic1 74 14 14 27
Q9QYB1 Chloride intracellular channel protein 4 Clic4 71 15 15 28.7
Q8BXK9 Chloride intracellular channel protein 5 Clic5 57 11 9 28.3

Table 6.

List of mass spectrometrically identified fatty acid binding proteins from mouse kidney.

Accession Protein Gene Coverage (%) Peptides Unique Peptides Molecular mass (kDa)
P12710 Fatty acid-binding protein FABP1, liver Fabp1 43 5 5 14.2
P11404 Fatty acid-binding protein FABP3, heart Fabp3 53 7 7 14.8
P04117 Fatty acid-binding protein FABP4, adipocyte Fabp4 65 8 8 14.6
Q05816 Fatty acid-binding protein FABP5, epidermal tisssue Fabp5 73 9 9 15.1
P51880 Fatty acid-binding protein FABP7, brain Fabp7 14 1 1 14.9

Table 7.

List of mass spectrometrically identified mouse kidney dystrophin and associated proteins.

Accession Protein Gene Coverage (%) Peptides Unique Peptides Molecular mass (kDa)
P11531 Dystrophin Dp140 Dmd 3 8 8 140
Q62165 Dystroglycan Dag1 14 12 12 96.8
Q61234 Alpha-1-syntrophin Snta1 22 8 8 53.6
Q61235 Beta-2-syntrophin Sntb2 34 13 13 56.3
O70258 Epsilon-sarcoglycan Sgce 3 1 1 49.7
Q9D2N4 Alpha-dystrobrevin Dtna 3 2 1 84
O70585 Beta-dystrobrevin Dtnb 16 6 5 74.4

2. Experimental design, materials, and methods

2.1. Biological samples and materials

The systematic cataloguing of the assessable kidney proteome was carried out with 12-month old wild type C57/BL6 mice and age-matched dystrophic mdx-4cv mice [9]. Animals were obtained from the Bioresource Unit of the University of Bonn [10] and kept under standard conditions and all procedures adhered to German legislation on the use of animals in experimental research.

For kidney protein extraction, protein digestion and the mass spectrometric analysis of the renal proteome, general materials and analytical grade reagents were purchased from Bio-Rad Laboratories (Hemel-Hempstead, Hertfordshire, UK), GE Healthcare (Little Chalfont, Buckinghamshire, UK) and Sigma Chemical Company (Dorset, UK). For the filter-aided sample preparation procedure, filter units Vivacon 500 (product number: VN0H22) were purchased from Sartorius (Göttingen, Germany). Protein digestion was carried out with sequencing grade modified trypsin from Promega (Madison, WI, USA). Pierce C18 spin columns and Acclaim PepMap 100 columns were from Thermo Fisher Scientific (Dublin, Ireland).

2.2. Kidney protein extraction and mass spectrometric analysis

Crude protein extracts were prepared as described in detail in the accompanying research paper [1]. The filter-aided sample preparation method was used as described by Wiśniewski et al. [11]. For the mass spectrometric establishment of the assessable mouse kidney proteome, peptide characterization was carried out by reverse-phased capillary high pressure liquid chromatography using an UltiMate 3000 nano system from Thermo Scientific [12]. The liquid chromatographic separation of peptides was coupled directly in-line with a Orbitrap Fusion Tribrid Mass Spectrometer from Thermo Scientific. Data analysis was carried out as previously described in detail [13].

Acknowledgments

Research was supported by Medical Research Charities Group grant HRB/MRCG-2016-20 from the Health Research Board and Muscular Dystrophy Ireland, as well as funding from the Kathleen Lonsdale Institute for Human Health Research at Maynooth University. The Orbitrap Fusion Tribrid mass spectrometer was funded under a Science Foundation Ireland Infrastructure Award to Dublin City University (SFI 16/RI/3701).

Conflict of Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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