High-intensity interval training remodels the proteome and acetylome of human skeletal muscle

  1. Morten Hostrup  Is a corresponding author
  2. Anders Krogh Lemminger
  3. Ben Stocks
  4. Alba Gonzalez-Franquesa
  5. Jeppe Kjærgaard Larsen
  6. Julia Prats Quesada
  7. Martin Thomassen
  8. Brian Tate Weinert
  9. Jens Bangsbo
  10. Atul Shahaji Deshmukh  Is a corresponding author
  1. Section of Integrative Physiology, Department of Nutrition, Exercise and Sports, University of Copenhagen, Denmark
  2. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark
  3. The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Denmark
  4. The Novo Nordisk Foundation Center for Protein Research, Clinical Proteomics, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark
8 figures, 1 table and 11 additional files

Figures

Figure 1 with 2 supplements
Physiological adaptations to HIIT.

(A) Experimental overview. (B). Subject characteristics. (C). Five weeks of HIIT increased maximal oxygen uptake (V̇O2max) and incremental peak power output (iPPO). (D) HIIT increased whole-body fat oxidation during submaximal exercise (50–150 W) without altering (E). carbohydrate oxidation. (F). HIIT increased mitochondrial respiration in skeletal muscle (LN: leak respiration, FAO: fatty acid oxidation, CID: submaximal CI respiration, PD: submaximal CI +II respiration, P: oxidative phosphorylation capacity, E: electron transport system capacity, ECII: succinate-supported electron transport system capacity). (G). HIIT increased skeletal muscle citrate synthase (CS) activity. (H). Analytical workflow. Summary statistics are mean ± SEM (n=8). * p<0.05, ** p<0.01, *** p<0.001.

Figure 1—figure supplement 1
CONSORT flow diagram of enrolled participants.
Figure 1—figure supplement 2
Proteome quality control.

(A) Quantified proteins from each sample. (B). Representative Pearson correlation between biological replicates (Pre 4 v Pre 5). (C). Cellular compartment (GOCC) coverage of the proteome. (D). Principal component analysis of the proteome. P: participant.

Figure 2 with 1 supplement
HIIT increases mitochondrial proteins and reduces a subset of contractile fiber associated proteins.

(A) Volcano plot displaying 102 upregulated and 24 downregulated proteins following HIIT (FDR <0.05). (B). Fisher’s exact tests identified the enrichment of mitochondrial terms within the differentially regulated proteins (enrichment analysis FDR <0.02). (C). Hierarchical clustering and enrichment analysis (enrichment analysis FDR <0.02) on differentially regulated proteins identified that mitochondrial terms are enriched within the upregulated proteins, while cytoplasm (UniProt Keyword) is enriched amongst the downregulated proteins. (D). Summed total protein abundances for different organelles (UniProt Keyword) shows upregulation of the mitochondrial protein content. (E–G). Summed total protein abundances display upregulation of electron transport chain complexes (E), mitochondrially encoded proteins (F) and proteins with a transit peptide (G). Summary statistics are mean ± SEM (n=8). * p<0.05, ** p<0.01, *** p<0.001.

Figure 2—figure supplement 1
HIIT increases electron transport chain subunits.

Immunoblotting analyses confirmed the upregulation of electron transport chain proteins. Representative images confirming equal loading are displayed in Figure 5—figure supplement 2. Summary statistics are mean ± SEM (n=8). * p<0.05, ** p<0.01, *** p<0.001.

Figure 2—figure supplement 1—source data 1

Full image and annotation of OXPHOS immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig2-figsupp1-data1-v1.pdf
Figure 2—figure supplement 1—source data 2

Raw ImageLab file of OXPHOS immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig2-figsupp1-data2-v1.zip
Figure 2—figure supplement 1—source data 3

Raw quantification data of OXPHOS immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig2-figsupp1-data3-v1.xlsx
Figure 3 with 1 supplement
HIIT regulates proteins involved in skeletal muscle calcium sensitivity and handling HIIT did not alter the abundance of myosin heavy chain (MYH1: MyHC2x, MYH2: MyHC2a, MYH4: MyHC2x, MYH7: MyHCβ; A) or light chain (B) isoforms.

(C). HIIT regulates proteins controlling myosin phosphorylation. (D). HIIT reduces abundance of subunits of the dihydropyridine receptor. (E). Summed total protein abundances display downregulation of the dihydropyridine receptor. (F). HIIT does not alter the abundance of ryanodine receptor 1. Summary statistics are mean ± SEM (n=8). ^ FDR <0.05. * p<0.05, ** p<0.01, *** p<0.001.

Figure 3—figure supplement 1
HIIT decreases MYLK2 abundance.

(A) Immunoblotting analysis confirms the downregulation of MYLK2. Representative images confirming equal loading are displayed in Figure 5—figure supplement 2. (B). No change in the abundance of sarcoplasmic/endoplasmic reticulum calcium ATPases 1–3 (SERCAs). Summary statistics are mean ± SEM (n=8). * p<0.05, ** p<0.01, *** p<0.001.

Figure 3—figure supplement 1—source data 1

Full image and annotation of MYLK2 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig3-figsupp1-data1-v1.pdf
Figure 3—figure supplement 1—source data 2

Raw ImageLab file of MYLK2 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig3-figsupp1-data2-v1.zip
Figure 3—figure supplement 1—source data 3

Raw quantification data of MYLK2 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig3-figsupp1-data3-v1.xlsx
Figure 4 with 1 supplement
The human skeletal muscle acetylome displays higher stoichiometry on mitochondrial proteins and lower stoichiometry on contractile proteins.

(A) We quantified 1263 acetyl-sites corresponding to 464 proteins (n=7). Of these, 421 proteins were also quantified in the proteome with 1232 of the quantified acetyl-sites located on these 421 proteins. (B). Distribution of acetyl-sites on proteins within the pre-HIIT acetylome. (C). Top 10 highest intensity acetylated proteins (acetyl-peptide intensities were summed for each protein) within the pre-HIIT acetylome. (D). Cumulative protein abundance and rank within the proteome (the top 10 highest intensity acetyl-proteins are highlighted). (E). One-dimensional enrichment analysis of acetylated protein intensity identified mitochondrial proteins, particularly those involved in carboxylic acid metabolism and monovalent inorganic cation transport (e.g. complex V) as having systematically high acetylation intensities (enrichment analysis FDR <0.02). (F). Top 10 acetyl-sites with highest abundance-corrected intensities (ACIs). (G). One-dimensional enrichment analysis of acetyl-site ACIs identified mitochondrial and carboxylic acid catabolic proteins as higher stoichiometry (positive enrichment factor), while contractile fiber cytosolic and plasma membrane proteins were enriched as lower stoichiometry negative enrichment factor; (enrichment analysis FDR <0.02; enrichment performed on leading protein IDs). (H). Histogram depicting the ACI distribution of the total acetylome (blue), the mitochondrial acetyl-sites (green) and the contractile fiber acetyl-sites (yellow). Mitochondrial proteins were distributed at higher ACI values and contractile fiber proteins at lower ACI values than the total acetylome.

Figure 4—figure supplement 1
Acetylome quality control.

(A) Overlap between identified acetyl-site with those identified in human skeletal muscle by Lundby et al., 2012. (B). Quantified acetyl-sites from each sample. (C). Representative Pearson correlation between biological replicates (Pre 4 v Pre 5). (D). Cellular compartment (GOCC) coverage of the acetylome. (E). Principal component analysis of the acetylome. P: participant.

Figure 5 with 2 supplements
HIIT increases acetylation of mitochondrial and TCA cycle proteins concomitantly with an increase in SIRT3 abundance.

(A) Volcano plot displaying 20 upregulated (filled red circles) and 1 downregulated (filled blue circle) acetyl-sites following HIIT at an FDR <0.05, while 257 acetyl-sites were upregulated (red circles) and 26 downregulated (blue circles) at Π<0.05 (n=7). (B). Scatter plot indicating that HIIT-induced changes in acetyl-site intensity typically exceeded that of the corresponding protein. (C). Fisher’s exact tests identified the enrichment of mitochondrial and TCA cycle terms within the differentially regulated acetyl-proteins (enrichment analysis FDR <0.02; enrichment performed on leading protein IDs). (D). IceLogo motif enrichment (p<0.01) for the upregulated sites displayed a predominance of proximal cysteine residues relative to the acetylated lysine (position 0). (E). Immunoblotting analysis identified the upregulation of the deacetylases SIRT3, SIRT5, and SIRT6, but no change in SIRT1, whilst the mitochondrial acetyltransferase GCN5L1 remained unchanged following HIIT (n=7–8). Representative images confirming equal loading are displayed in Figure 5—figure supplement 2. * p<0.05, ** p<0.01, *** p<0.001.

Figure 5—source data 1

Full image and annotation of SIRT1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data1-v1.pdf
Figure 5—source data 2

Raw ImageLab file of SIRT1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data2-v1.zip
Figure 5—source data 3

Raw quantification data of SIRT1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data3-v1.xlsx
Figure 5—source data 4

Full image and annotation of SIRT3 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data4-v1.pdf
Figure 5—source data 5

Raw ImageLab file of SIRT3 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data5-v1.zip
Figure 5—source data 6

Raw quantification data of SIRT3 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data6-v1.xlsx
Figure 5—source data 7

Full image and annotation of SIRT5 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data7-v1.pdf
Figure 5—source data 8

Raw ImageLab file of SIRT5 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data8-v1.zip
Figure 5—source data 9

Raw quantification data of SIRT5 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data9-v1.xlsx
Figure 5—source data 10

Full image and annotation of SIRT6 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data10-v1.pdf
Figure 5—source data 11

Raw ImageLab file of SIRT6 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data11-v1.zip
Figure 5—source data 12

Raw quantification data of SIRT6 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data12-v1.xlsx
Figure 5—source data 13

Full image and annotation of GCN5L1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data13-v1.pdf
Figure 5—source data 14

Raw ImageLab file of GCN5L1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data14-v1.zip
Figure 5—source data 15

Raw quantification data of GCN5L1 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-data15-v1.xlsx
Figure 5—figure supplement 1
HIIT increases protein acetylation.

(A) Immunoblotting analysis confirmed the upregulation of acetylation following HIIT (n=7). (B) Immunoblotting analysis confirmed the upregulation of acetylation on K68 (n=8) and K122 (n=7) of SOD2 following HIIT. Representative images confirming equal loading are displayed in Figure 5—figure supplement 2. * p<0.05, ** p<0.01, *** p<0.001.

Figure 5—figure supplement 1—source data 1

Full image and annotation of Pan-acetyl immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data1-v1.pdf
Figure 5—figure supplement 1—source data 2

Raw ImageLab file of Pan-acetyl immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data2-v1.zip
Figure 5—figure supplement 1—source data 3

Raw quantification data of Pan-acetyl immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data3-v1.xlsx
Figure 5—figure supplement 1—source data 4

Full image and annotation of ac-SOD2 K68 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data4-v1.pdf
Figure 5—figure supplement 1—source data 5

Raw ImageLab file of ac-SOD2 K68 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data5-v1.zip
Figure 5—figure supplement 1—source data 6

Raw quantification data of ac-SOD2 K68 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data6-v1.xlsx
Figure 5—figure supplement 1—source data 7

Full image and annotation of ac-SOD2 K122 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data7-v1.pdf
Figure 5—figure supplement 1—source data 8

Raw ImageLab file of ac-SOD2 K122 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data8-v1.zip
Figure 5—figure supplement 1—source data 9

Raw quantification data of ac-SOD2 K122 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp1-data9-v1.xlsx
Figure 5—figure supplement 2
Representative images of equal loading for immunoblot analyses.

(A) Coomassie stain for n=8 immunoblots of human skeletal muscle (Figure 5E (SIRT1-6), Figure 7E, Figure 2—figure supplement 1, and Figure 3—figure supplement 1). (B). Stain-free image for n=7 immunoblots of human skeletal muscle (Figure 5E (GCN5L1), and Figure 5—figure supplement 1A). (C). Stain-free image for EP300 KD immunoblots (Figure 7F).

Figure 5—figure supplement 2—source data 1

Full image and annotation of n=8 Coomassie stain.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data1-v1.pdf
Figure 5—figure supplement 2—source data 2

Raw ImageLab file of n=8 Coomassie stain.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data2-v1.zip
Figure 5—figure supplement 2—source data 3

Full image and annotation of n=7 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data3-v1.pdf
Figure 5—figure supplement 2—source data 4

Raw ImageLab file of n=7 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data4-v1.zip
Figure 5—figure supplement 2—source data 5

Full image and annotation of C2C12 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data5-v1.pdf
Figure 5—figure supplement 2—source data 6

Raw ImageLab file of C2C12 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig5-figsupp2-data6-v1.zip
Individual acetyl-site regulation of mitochondrial, TCA cycle and contractile proteins following HIIT.

Regulation of acetyl-sites on (A). electron transport chain complex subunits (annotated by HUGO), (B) TCA cycle proteins (annotated by KEGG) and (C) muscle contraction proteins (annotated by REACTOME).

Figure 7 with 1 supplement
HIIT increases acetylation on specific histone acetyl-sites.

HIIT increased acetylation on (A). H1.5 K48, (B). H2B type 2F K16/20 and (C). H3 K23. (D). HIIT did not alter H4 acetylation (n=7). (E) Immunoblotting analysis identified the upregulation of the nuclear-localized acetyltransferase EP300 (n=8, mean of three technical replicates; participant 1 was excluded as an outlier from statistical analysis (pre, post and fold-change values were all >3 median absolute deviations from the respective median), data for participant 1 is shown in the translucent data points). (F) Knockdown of EP300 reduces acetylation of H2B K20 but not H3 K23 in C2C12 myotubes (n=3). Representative images confirming equal loading are displayed in Figure 5—figure supplement 2. Summary statistics are mean ± SEM. † Π<0.05. * p<0.05, ** p<0.01, *** p<0.001.

Figure 7—source data 1

Full image and annotation of H2B immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data1-v1.pdf
Figure 7—source data 2

Raw ImageLab file of H2B immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data2-v1.zip
Figure 7—source data 3

Full image and annotation of H2B K20 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data3-v1.pdf
Figure 7—source data 4

Raw ImageLab file of H2B K20 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data4-v1.zip
Figure 7—source data 5

Raw quantification data of H2B K20/H2B immunoblots.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data5-v1.xlsx
Figure 7—source data 6

Full image and annotation of H3 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data6-v1.pdf
Figure 7—source data 7

Raw ImageLab file of H3 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data7-v1.zip
Figure 7—source data 8

Full image and annotation of H3 K23 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data8-v1.pdf
Figure 7—source data 9

Raw ImageLab file of H3 K23 immunoblot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data9-v1.zip
Figure 7—source data 10

Raw quantification data of H3 K20/H3 immunoblots.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data10-v1.xlsx
Figure 7—source data 11

Full image and annotation of EP300 immunoblots (human skeletal muscle).

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data11-v1.pdf
Figure 7—source data 12

Raw ImageLab file of EP300 immunoblots (human skeletal muscle, replicate 1).

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data12-v1.zip
Figure 7—source data 13

Raw ImageLab file of EP300 immunoblots (human skeletal muscle, replicates 2 & 3).

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data13-v1.zip
Figure 7—source data 14

Raw quantification data of EP300 immunoblot (human skeletal muscle).

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-data14-v1.xlsx
Figure 7—figure supplement 1
Normalization of EP300.

Normalization of EP300. EP300 displays a similar increase following HIIT without normalization (A) or when normalized to a stain-free blot (B). Data taken from replicate 1 of EP300 immunoblotting. (C) Images of EP300 immunoblot and stain-free blot for replicate 1 of EP300 immunoblotting.

Figure 7—figure supplement 1—source data 1

Full image and annotation of EP300 (human skeletal muscle) replicate 1 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-figsupp1-data1-v1.pdf
Figure 7—figure supplement 1—source data 2

Raw ImageLab file of EP300 (human skeletal muscle) replicate 1 stain-free blot.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-figsupp1-data2-v1.zip
Figure 7—figure supplement 1—source data 3

Raw quantification data of EP300 (human skeletal muscle) replicate 1 with and without normalization.

https://cdn.elifesciences.org/articles/69802/elife-69802-fig7-figsupp1-data3-v1.xlsx
Author response image 1
No change in (A) pan-lysine acetylation, or (B) H2B K20 acetylation following 24 hours of electrical pulse stimulation in C2C12 myotubes (n = 6/ group).

Tables

Appendix 1—key resources table
Reagent type (species) or resourceDesignationSource or referenceIdentifiersAdditional information
AntibodyMYLK2 Antibody, rabbit polyclonal
InvitrogenCat#PA5-29324
RRID: AB_2546800
(1:1000)
AntibodyTotal OXPHOS Human WB Antibody Cocktail, mouse monoclonalAbcamCat#ab110411
RRID: AB_2756818
(1:1000)
AntibodySirt1(Sir2) Antibody, rabbit polyclonalMillipore SigmaCat#07–131
RRID: AB_10067921
(1:1000)
AntibodySirt3 (D22A3) Antibody, rabbit monoclonalCell Signaling TechnologiesCat#5490
RRID: AB_10828246
(1:2000)
AntibodySirt5 Antibody, rabbit monoclonalCell Signaling TechnologiesCat#8782
RRID: AB_2716763
(1:1000)
AntibodySirt6 Antibody, rabbit monoclonalCell Signaling TechnologiesCat#12486
RRID: AB_2636969
(1:1000)
AntibodyAcetyl-lysine Antibody, rabbit polyclonalCell Signaling TechnologiesCat#9441
RRID: AB_331805
(1:1000)
AntibodyAc-SOD2 K68 Antibody, rabbit monoclonalAbcamCat#ab13737
RRID: AB_2784527
(1:1000)
AntibodyAc-SOD2 K122 Antibody, rabbit monoclonalAbcamCat#ab214675
RRID: AB_2892634
(1:1000)
AntibodyP300 Mouse Antibody, mouse monoclonalSanta Cruz BiotechnologiesCat#sc48343
RRID: AB_628075
(1:200)
AntibodyP300 Mouse Antibody, mouse monoclonalSanta Cruz BiotechnologiesCat#sc32244
RRID: AB_628076
(1:500)
AntibodyAc-H2B K20 Antibody, rabbit monoclonalAbcamCat#ab177430(1:1000)
AntibodyH2B Antibody, rabbit monoclonalCell Signaling TechnologiesCat#12364
RRID: AB_2714167
(1:3000)
AntibodyAc-H3 K23 Antibody, rabbit monoclonalCell Signaling TechnologiesCat#14932
RRID: AB_2798650
(1:1000)
AntibodyH3 Antibody, rabbit monoclonalCell Signaling TechnologiesCat#4499
RRID: AB_10544537
(1:3000)
AntibodyGoat Anti-Rabbit Ig, Human ads-HRP, goat polyclonalSouthern BiotechCat#4010–05
RRID: AB_2632593
(1:5000)
AntibodyGoat Anti-Mouse, goat polyclonalDako (Agilent)Cat# P0447
RRID: AB_2617137
(1:5000)
Biological sample (human)Human skeletal muscle (vastus lateralis)This paperNot externally available
Cell line (mouse)C2C12 (ATCC CRL-1772)ATCCCat#1722
RRID: CVCL_0188
Authenticated by ATCC – CO1 assay. Tested in-house for mycoplasma – negative.
Chemical compound, drugGlycerolMillipore SigmaCat# G5516; CAS# 56-81-5
Chemical compound, drugSodium pyrophosphate decahydrateMillipore SigmaCat# 221368; CAS# 13472-36-1
Chemical compound, drugSodium chlorideMillipore SigmaCat# S9888; CAS# 7647-14-5
Chemical compound, drugHEPESMillipore SigmaCat# H3375; CAS# 7365-45-9
Chemical compound, drugIGEPAL CA-630, NP-40Millipore SigmaCat# I8896; CAS# 9002-93-1
Chemical compound, drugβ-Glycerophosphate disodium salt hydrateMillipore SigmaCat# G9422; CAS# 154804-51-0
Chemical compound, drugSodium orthovanadateMillipore SigmaCat# S6508; CAS# 13721-39-6
Chemical compound, drugSodium fluorideMillipore SigmaCat# S1504; CAS# 7681-49-4
Chemical compound, drugPhenylmethanesulfonyl fluorideMillipore SigmaCat# P7626; CAS# 329-98-6
Chemical compound, drugEDTA (for electrophoresis)Millipore SigmaCat# E5134; CAS# 6381-92-6
Chemical compound, drugEGTAMillipore SigmaCat# E4378; CAS# 67-42-5
Chemical compound, drugAprotinin from bovine lungMillipore SigmaCat# A1153; CAS# 9087-70-1
Chemical compound, drugLeupeptinMillipore SigmaCat# L2884; CAS# 103476-89-7
Chemical compound, drugBenzamidine hydrochloride hydrateMillipore SigmaCat# B6506; CAS# 206752-36-5
Chemical compound, drugBovine serum albuminMillipore SigmaCat# A7906; CAS# 9048-46-8
Chemical compound, drugTrizma baseMillipore SigmaCat# T1503; CAS# 77-86-1
Chemical compound, drugDL-DithiothreitolMillipore SigmaCat# D0632 and 43819; CAS# 3483-12-3
Chemical compound, drugSodium dodecyl sulfateMillipore SigmaCat# L3771; CAS# 151-21-3
Chemical compound, drugBromophenol Blue sodium saltMillipore SigmaCat# B8026; CAS# 34725-61-6
Chemical compound, drugTween 20Millipore SigmaCat# P9416; CAS# 9005-64-5
Chemical compound, drugSkimmed milk powderEasisCat# 801,300
Chemical compound, drugGlycineMillipore SigmaCat# G7126; CAS# 56-40-6
Chemical compound, drug2-propanolMillipore SigmaCat# 109634; CAS# 67-63-0
Chemical compound, drugEthanol 96%PlumCat# 201146; CAS# 64-17-5
Chemical compound, drugBrilliant Blue RMillipore SigmaCat# B7920; CAS# 6104-59-2
Chemical compound, drugAcetic acid (glacial) 100%Millipore SigmaCat# 100063; CAS# 64-19-7
Chemical compound, drugPrecision plus all blueBioRadCat# 1610373
Chemical compound, drugPrecision plus dual colorBioRadCat# 1610374
Chemical compound, drugImmobilon Forte Western HRP substrateMillipore SigmaCat# WBLUF 0500
Chemical compound, drugBovine Serum Albumin StandardThermo Fisher ScientificCat# 23,209
Chemical compound, drugBCA Protein Assay Reagent AThermo Fisher ScientificCat# 23,223
Chemical compound, drugBCA Protein Assay Reagent BThermo Fisher ScientificCat# 23,224
Chemical compound, drugPotassium phosphate dibasic trihydrateMillipore SigmaCat# P9666; CAS# 16788-57-1
Chemical compound, drugPotassium dihydrogen phosphateMillipore SigmaCat# 1.04873; CAS# 7778-77-0
Chemical compound, drugBCA Protein Assay KitThermo Fisher ScientificCat# 23,225
Chemical compound, drugTrizma hydrochlorideMillipore SigmaCat# T3253; CAS# 1185-53-1
Chemical compound, drugEDTAMillipore SigmaCat# E9884; CAS# 60-00-4
Chemical compound, drugNADMillipore SigmaCat# NAD100-RO; CAS# 53-84-9
Chemical compound, drugL-(−)-Malic acid sodium saltMillipore SigmaCat# M1125; CAS# 68303-40-2
Chemical compound, drugAcetyl-Coenzyme AMillipore SigmaCat# ACOA-RO
Chemical compound, drugL-Malate Dehydrogenase (L-MDH)Millipore SigmaCat# LMDH-RO
Chemical compound, drugNADHMillipore SigmaCat# 10107735001
Chemical compound, drugSucroseMillipore SigmaCat# S7903; CAS# 57-50-1
Chemical compound, drugMagnesium chloride hexahydrateMillipore SigmaCat# M2670; CAS# 7791-18-6
Chemical compound, drugTaurineMillipore SigmaCat# T0625; CAS# 107-35-7
Chemical compound, drugPotassium Dihydrogen PhosphateMillipore SigmaCat# P9791; CAS# 7778-77-0
Chemical compound, drugHEPESMillipore SigmaCat# H3375; CAS# 7365-45-9
Chemical compound, drugBovine serum albumin (fatty acid free)Millipore SigmaCat# A7030; CAS# 9048-46-8
Chemical compound, drugCatalase from bovine liverMillipore SigmaCat# C9322; CAS# 9001-05-2
Chemical compound, drugLactobionic acidMillipore SigmaCat# 153516; CAS# 96-82-2
Chemical compound, drugMES potassium saltMillipore SigmaCat# M0895; CAS# 39946-25-3
Chemical compound, drugATPMillipore SigmaCat# A3377; CAS# 34369-07-8
Chemical compound, drugSodium creatine phosphate dibasic tetrahydrateMillipore SigmaCat# 27920; CAS# 71519-72-7
Chemical compound, drugImidazoleMillipore SigmaCat# I0250; CAS# 288-32-4
Chemical compound, drugPotassium hydroxideMillipore SigmaCat# P1767; CAS# 1310-58-3
Chemical compound, drugCalcium carbonateMillipore SigmaCat# C4830; CAS# 471-34-1
Chemical compound, drugSaponin from quillaja barkMillipore SigmaCat# S7900; CAS# 8047-15-2
Chemical compound, drugL-(−)-Malic acid sodium saltMillipore SigmaCat# M1125; CAS# 68303-40-2
Chemical compound, drugOctanoyl-L-carnitineMillipore SigmaCat# 50892; CAS# 25243-95-2
Chemical compound, drugADPMillipore SigmaCat# A5285; CAS# 72696-48-1
Chemical compound, drugL-glutamic acid monosodium salt monohydrateMillipore SigmaCat# 49621; CAS# 6106-04-3
Chemical compound, drugSodium succinate dibasic hexahydrateMillipore SigmaCat# S2378; CAS# 6106-21-4
Chemical compound, drugCytochrome c from equine heartMillipore SigmaCat# C2506; CAS# 9007-43-6
Chemical compound, drugFCCPMillipore SigmaCat# C2920; CAS# 370-86-5
Chemical compound, drugRotenoneMillipore SigmaCat# R8875; CAS# 83-79-4
Chemical compound, drugMalonic acidMillipore SigmaCat# M1296; CAS# 141-82-2
Chemical compound, drugMyxothiazolMillipore SigmaCat# T5580; CAS# 76706-55-3
Chemical compound, drugAntimycin A from Streptomyces sp.Millipore SigmaCat# A8674; CAS# 1397-94-0
Chemical compound, drugSodium deoxycholateSigma-AldrichCat# D6750
CAS# 302-95-4
Chemical compound, drugTris(2-carboxyethyl)phosphine hydrochlorideSigma-AldrichCat# C4706
CAS# 51805-45-9
Chemical compound, drug2-ChloroacetamideSigma-AldrichCat# 22,790
CAS# 79-07-2
Chemical compound, drugTrypsinSigma-AldrichCat# T7575
Chemical compound, drugLysineWakoCat# 124–06871
Chemical compound, drugDMEM high glucoseGibcoCat# 41965039
Chemical compound, drugFetal bovine serum(FBS)Sigma-AldrichCat# F7524
Chemical compound, drugPenicillin-Streptomycin, liquidGibcoCat# 15070–063
Chemical compound, drugOpti-MEM I Reduced Serum MediumGibcoCat# 31985062
Chemical compound, drugTransIT-X2 Dynamic Delivery SystemMirus BioCat# MIR6003
Sequence-based reagentEP300 siRNAMerck SigmaCat# SASI_Mm01_00159721
Commercial assay or kitPTMScan Acetyl-Lysine Motif [Ac-K] KitCell Signaling TechnologiesCat#13,416
Software, algorithm,Graphpad Prism 8.0https://www.graphpad.com/RRID: SCR_002798
Software, algorithmMaxQuant 1.5.3.30https://maxquant.org/RRID: SCR_014485
Software, algorithmSpectronaut v14https://biognosys.com/shop/spectronaut
Software, algorithmPerseus 1.6.10.50http://www.coxdocs.org/doku.php?id=perseus:startRRID: SCR_015753
Software, algorithmR Studiohttps://rstudio.com/RRID: SCR_000432
Software, algorithmCytoscape v3.7.2https://www.cytoscape.orgRRID: SCR_003032
Software, algorithmiceLogohttps://iomics.ugent.be/icelogoserver/RRID: SCR_012137
Software, algorithmAdobe Illustrator 24.3https://www.adobe.com/products/illustratorRRID: SCR_010279
Software, algorithmBio-Rad Image Studiohttps://www.licor.com/bio/products/Software, algorithm/image_studio/RRID: SCR_014210
Software, algorithmOroboros DatLab 6 V. 6.1.0.7https://www.oroboros.at/index.php/product/datlab/
OtherStainless Steel Beads 5 mmQiagenCat# 69989Lysis reagent
OtherStuart Rotator Drive STR4Stuart-equipmentCat# STR4Lysis reagent
OtherHettich universal 320 R centrifugeAndrea Hettich GmbH, GermanyCat# 1406Lysis reagent
OtherEmax precision microplate readerMolecular DevicesCat# LR88026Protein concentration quantification
OtherWhite 96-Well Immuno PlatesFischer ScientificCat# 10415985Protein concentration quantification
OtherFluoroskan, Microplate Fluorometer, one dispenserFischer ScientificCat# 5200111Protein concentration quantification
OtherMultiskan FC Microplate PhotometerFischer ScientificCat# 11500695Protein concentration quantification
OtherPowerPac HC Power SupplyBioRadCat# 1645052Immunoblotting reagent
OtherTE 77 ECL Semi-Dry Transfer UnitAmersham BiosciencesCat# 80-6211-86Immunoblotting reagent
OtherChemiDoc MP Imaging SystemBioRadCat# 731BR00119Immunoblotting reagent
Other10% Criterion TGX Stain-Free gelBioRadCat# 567–8035Immunoblotting reagent
Other16.5% Criterion Tris-Tricine/Peptide gelBioRadCat# 345–0065Immunoblotting reagent
OtherImmobilon-P PVDF membraneMillipore SigmaCat# IPVH00010Immunoblotting reagent
OtherWhatman cellulose chromatography papersMillipore SigmaCat# WHA3030917Immunoblotting reagent
OtherSep-Pak C18 CartrigeWatersCat# WAT054955Proteomic sample preparation
OtherNon-treated 96-Well MicroplatesFischer ScientificCat# 10252711Proteomic sample preparation

Additional files

Supplementary file 1

Identified proteins.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp1-v1.xlsx
Supplementary file 2

Quantified proteins and their regulation by HIIT.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp2-v1.xlsx
Supplementary file 3

Fisher’s exact test of HIIT-regulated proteins (FDR <0.05).

https://cdn.elifesciences.org/articles/69802/elife-69802-supp3-v1.xlsx
Supplementary file 4

Identified acetyl-sites.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp4-v1.xlsx
Supplementary file 5

Quantified acetyl-sites and their regulation by HIIT.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp5-v1.xlsx
Supplementary file 6

Summed acetylation intensity per protein.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp6-v1.xlsx
Supplementary file 7

One-dimensional enrichment analysis of summed acetylation intensity.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp7-v1.xlsx
Supplementary file 8

Abundance corrected intensities (ACIs) of acetyl-sites pre-HIIT.

https://cdn.elifesciences.org/articles/69802/elife-69802-supp8-v1.xlsx
Supplementary file 9

One-dimensional enrichment analysis of pre-HIIT acetyl-site ACI (Leading protein ID was used for relative enrichment).

https://cdn.elifesciences.org/articles/69802/elife-69802-supp9-v1.xlsx
Supplementary file 10

Fisher’s exact test of HIIT-regulated (Π<0.05) acetyl-sites (Leading protein ID was used for relative enrichment).

https://cdn.elifesciences.org/articles/69802/elife-69802-supp10-v1.xlsx
Transparent reporting form
https://cdn.elifesciences.org/articles/69802/elife-69802-transrepform1-v1.docx

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  1. Morten Hostrup
  2. Anders Krogh Lemminger
  3. Ben Stocks
  4. Alba Gonzalez-Franquesa
  5. Jeppe Kjærgaard Larsen
  6. Julia Prats Quesada
  7. Martin Thomassen
  8. Brian Tate Weinert
  9. Jens Bangsbo
  10. Atul Shahaji Deshmukh
(2022)
High-intensity interval training remodels the proteome and acetylome of human skeletal muscle
eLife 11:e69802.
https://doi.org/10.7554/eLife.69802