{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/06/PXD033198/20210608_Myo19.xlsx"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/06/PXD033198/20210608_Myo19_2_1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/06/PXD033198/20210608_con_1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/06/PXD033198/20210608_Myo19_1_1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2022/06/PXD033198/20210608_con_2.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["congyingwu@bjmu.edu.cn"],"submitter":["Xiaoyu Ren"],"technology_type":["Affinity purification coupled with mass spectrometry proteomics","Mass Spectrometry"],"software":["Not available"],"submitter_keywords":["Myo19 ip-ms"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD033198"],"tissue":["Cell Culture"],"sample_protocol":["Lysis->Myo19 antibody->protein A/G beads ->SDS-PAGE gels->MS"],"repository":["Pride"],"modification":[""],"quantification_method":["Not available"],"data_protocol":["MS/MS spectra data were acquired in the Orbitrap as well with a resolution of 15,000 (FWHM) at m/z 200 Da and AGC target value for fragment spectra was set at 100% with a maximum IT of 22 ms. Isolation width was 1.6 m/z. Normalized collision energy was set at 30%. FAIMS CV were set as -45V and -65V. The MS data were aligned with UniProtKB/Swiss-Prot reviewed human proteome database."],"omics_type":["Proteomics"],"labhead":["Congying Wu"],"instrument_platform":[""],"labhead_affiliation":["Institute of Systems Biomedicine, Peking University Health Science Center, Beijing 100191, China."],"species":["Homo Sapiens (human)"],"submission_type":["PARTIAL"],"publication":["35562374 Shi P, Ren X, Meng J, Kang C, Wu Y, Rong Y, Zhao S, Jiang Z, Liang L, He W, Yin Y, Li X, Liu Y, Huang X, Sun Y, Li B, Wu C. Mechanical instability generated by Myosin 19 contributes to mitochondria cristae architecture and OXPHOS. Nat Commun. 2022 13(1):2673 10.1038/s41467-022-30431-3"],"submitter_mail":["xiaoyuren@pku.edu.cn"],"submitter_affiliation":["Institute of Systems Biomedicine, Peking University Health Science Center, Beijing 100191, China."],"submitter_country":["China"],"pubmed_abstract":["The folded mitochondria inner membrane-cristae is the structural foundation for oxidative phosphorylation (OXPHOS) and energy production. By mechanically simulating mitochondria morphogenesis, we speculate that efficient sculpting of the cristae is organelle non-autonomous. It has long been inferred that folding requires buckling in living systems. However, the tethering force for cristae formation and regulation has not been identified. Combining electron tomography, proteomics strategies, super resolution live cell imaging and mathematical modeling, we reveal that the mitochondria localized actin motor-myosin 19 (Myo19) is critical for maintaining cristae structure, by associating with the SAM-MICOS super complex. We discover that depletion of Myo19 or disruption of its motor activity leads to altered mitochondria membrane potential and decreased OXPHOS. We propose that Myo19 may act as a mechanical tether for effective ridging of the mitochondria cristae, thus sustaining the energy homeostasis essential for various cellular functions."],"pubmed_title":["Mechanical instability generated by Myosin 19 contributes to mitochondria cristae architecture and OXPHOS."],"pubmed_authors":["Shi Peng P, Ren Xiaoyu X, Meng Jie J, Kang Chenlu C, Wu Yihe Y, Rong Yingxue Y, Zhao Shujuan S, Jiang Zhaodi Z, Liang Ling L, He Wanzhong W, Yin Yuxin Y, Li Xiangdong X, Liu Yong Y, Huang Xiaoshuai X, Sun Yujie Y, Li Bo B, Wu Congying C"],"sample_synonyms":["RGD1559961, Peptide P-C, Proactivator polypeptide, sodium dodecyl sulphate–polyacrylamide gel electrophoresis., Parotid double-band protein, Pa, Saposin-A, Parotid isoelectric focusing variant protein, Gel Electrophoresis, B-cell receptor complex, PRP-3|PRP-4, Co-beta-glucosidase, antibodies, SDS polyacrylamide gel electrophoresis of proteins, antibody, Db-s, Sodium Dodecyl Sulfate PAGE, BCR complex, Parotid acidic protein, Polyacrylamide Gel Electrophoresis, SDS-PAGE, bacteriocin activity, Sphingolipid activator protein 2, immunoglobulin complex, A1 activator, opsonin activity, MYOHD1, Salivary acidic proline-rich phosphoprotein 1|2, PRP-1|PRP-2, Pr1|Pr2, Polyacrylamide, holin, Salivary acidic proline-rich phosphoprotein 3|4, Sphingolipid activator protein 1, SDS-PAGE electrophoresis, Sodium Dodecyl Sulfate-PAGE, membrane bound, Parotid proline-rich protein 1|2, Saposin-B-Val, Dispersin, SDS polyacrylamide gel electrophoresis, CSAct, SAP-1, SAP-2, Staphylococcal, immunoglobulin, Cerebroside sulfate activator, Component C, lysin activity, 1110055A02Rik, B cell receptor accessory molecule complex, Protein C, Saposin-D, Saposin-C, Protein A, Saposin-B, B lymphocyte receptor complex, PIF-F, bacteriolytic toxin activity, Myohd1, B cell receptor activity, Sulfatide|GM1 activator, autolysin activity, necrosis, Db-F, Sodium Dodecyl Sulfate-PAGEs, B-lymphocyte receptor complex, PIF-S, Glucosylceramidase activator, SDS PAGE"],"name_synonyms":["Myohd1, Protein Gene Products, Gene Products, Proteins, MYOHD1, Gene Proteins, Gene, RGD1559961, 1110055A02Rik, Protein., Protein"],"data_synonyms":["phapii, FAIMS CV, IPP2A2, human being, Modern, igaad, StF-IT-1, total expressed protein, Th, Data Base., thomson, not genetically inherited, PHAPII, group, mass-to-charge ratio, Human, 5730420M11Rik, Homo sapiens, I-2PP2A, Dm I-2, I2PP2A, FWHM, Man, tandem MS, SET, HLA-DR-associated protein II, Man (Taxonomy), ensemble, DI-2, TAF-I, MS/MS, MS2, I-2Dm, ipp2a2, 2pp2a, CG4299, CG10574, human, DmelCG4299, I-2PP1, IGAAD, set, dSET/TAF-Ibeta, 2610030F17Rik, TAF-IBETA, 2PP2A, DmelCG10574, taf-ibeta, Modern Man, dSET, dSet, TAF-Ibeta, AA407739, i2pp2a, Proteomes"],"description_synonyms":["act57b, Act5c, DmelCG5178, l(1)G0010, act 87E, DmelCG7478, Act87e, ACT5C, Gene, beta-Actin, CG12051, Mitochondrial Contractions, anon-EST:CL2c12, Act5, l(1)G0420, act57B, DmelCG12051, l(1)G0025, CG30294, act57A, act 88F, Act88f, gamma Actin, Gene Products, Mitochondrion, actin-12, 143060_f_at, alpha-Actin, A, rsd, C, D, act5C, E, N Actin, cyt5C, DmelCG10067, M, Contraction, F-Actin, mus79B, Act57, beta Actin, act88F, anon-EST:fe2D2, Act42a, Isoactin, CG18290, N-Actin, act 42A, Ac5C, CG4027, T10, Act, T11, G-Actin, DmelCG18290, Act-5C, act87E, alpha Actin, l(1)G0177, Ifm(3)7, 42A, RGD1559961, l(1)G0330, Actin/BAP47, act 79B, Proteins, alpha Isoactin, act, BEST:RE38067, act42A, Contractions, ACTIN, beta-actin, AFFX-Dros-ACTIN_M_r_at, Protein, M32055, actin, Act42, CG7478, CG5178, CG10067, Act57A, l(1)G0079, MYOHD1, Mitochondrial, G Actin, DmelCG4027, Act88-F, l(1)G0117, act 57A, 1110055A02Rik., act 5C, Actin, gamma-Actin, beta-actin/Bap47, Act57b, mus87E, alpha-Isoactin, Protein Gene Products, Mitochondrial Contraction, l(1)G0486, act79B, Gene Proteins, l(1)G0245, actin5C, mitochondria, l(1)G0009, Act(88F), F Actin, Myohd1, BAP47, Bap47, Actin5C"],"pubmed_abstract_synonyms":["DmelCG5178, act 87E, DmelCG7478, l(3)Ca, Activity, 2410041A17Rik, ACTG, Motor Activity, Membrane Potential, ACTE, Physical, morphogenesis, beta-Actin, Imaging, d-titin, fs(1)M34, Organelle, Foundation, Mitochondrial Contractions, Act5, csp2, Social Controls, l(1)G0420, DmelCG12051, dmTAF[[II]]230, Actin Activated, Membrane Tissues, Motor, act 88F, Oxidative, gamma Actin, motor activity, DmelCG1915, HEL-176, CG4601, Transmembrane Potential Differences, present in fewer numbers in organism, Formal Social Controls, Ket, A, rsd, C, D, E, N Actin, cyt5C, TFIID TAF250, Motor Activities, pre-mortem, DHO, cel, M, S-adenosylmethionine, Differences, long, membrane region, Tissue, Myosin ATPase, CG18572, beta-particle, regulation of energy homeostasis., S-(5'-deoxyadenosin-5'-yl)-L-methionine, beta Actin, act88F, ket, Fast, Social, Delta Psi, Isoactin, e, decreased, Adenosinetriphosphatase, e-, N-Actin, act 42A, Transmembrane Potentials, Ac5C, CG4027, ACT, Act, MHC16, G-Actin, DmelCG18290, act87E, inner salt, Membrane Tissue, dTAF[[II]]230, l(1)G0330, OXPHOS, Actin/BAP47, Difference, Resting Potential, CTE-II, NMHC-II-C, AACT, cristae, alpha Isoactin, titin, mitochondrial cristae, TAF200, Actin Activated ATPase, CTE-IIa, integral to membrane, act, Ach1, hBACH, ACH1, Positrons, 0020/01, negative regulation of energy homeostasis, TAFII-250, TAF250/230, LACH1, act42A, SAMe, GIG25, ACTIN, TAFII250, Su(b), Alpha-1-antichymotrypsin His-Pro-less, AFFX-Dros-ACTIN_M_r_at, GIG24, Fast Electron, DFNA26, actin, NMHC II-C, CG7478, CG5178, LACH, GAT, DFNA20, CG10067, Act57A, DFNA4, Phosphorylation, Mitochondrial, Potential Differences, DmelCG4027, l(1)G0117, Myosin Adenosine Triphosphatase, Control, Actin, gamma-Actin, Electron, Controls, CG17603, TAF[[II]], beta-actin/Bap47, 5-dideoxy-beta-D-ribofuranos-5-yl][(3S)-3-amino-3-carboxypropyl](methyl)sulfonium, Act57b, beta(-), l(1)G0486, act79B, Activities, l(1)G0245, living, CG1915, actin5C, 1110055A02Rik, l(1)G0009, Taf250, ACTL3, SR3-5, Resting Potentials, Lach1, CG18242, Resting Membrane Potentials, Regulation, BACH, TAF230, CG18245, act57b, l(1)Ab, Regulations, Act5c, d230, l(1)G0010, Transmembrane, localised, Act87e, DFNA4A, Myosin Adenosinetriphosphatase, conformation, Peptidomics, Potential, e(-), ACT5C, CG12051, dTAFII250, electron, Potential Difference, Serpin A3, [1-(adenin-9-yl)-1, EfW1, anon-EST:CL2c12, SLS, Sls, Bach, Locomotor, act57B, l(1)G0025, CG30294, Tomographies, act57A, MYH17, Act88f, myosin 1, Actin-Activated ATPase, reduced, dmTAF1, Taf230, subnumerary, integral component of membrane, AdoMet, Mitochondrion, actin-12, Cell growth-inhibiting gene 24|25 protein, Titin, anon-CREST, 143060_f_at, l(3)j1D7, TAF250, alpha-Actin, Taf200, act5C, dTAF[[II]]250, localized, DmelCG10067, Transmembrane Electrical Potential Difference, Tissues, cell, Transmembrane Potential, Contraction, BRWS2, Elektron, F-Actin, mus79B, Taf1p, Act57, positive regulation of energy homeostasis, Locomotor Activity, CG18857, decreased number, respiratory-chain phosphorylation, fs(1)829, dTAF250, anon-EST:fe2D2, Act42a, l(3)dre8, Oxidative Phosphorylations, ATPase, 1700027G07Rik, embryogenesis and morphogenesis, CG18290, myosin, DmelCG18572, S-Adenosylmethionine, KZ, region of membrane, T10, l(3)rL182, T11, TAF, Act-5C, MCP, Cte-II, alpha Actin, Electrons, Positron, l(1)G0177, Ifm(3)7, membrane, anatomical structure organization, 42A, TAF[[II]]250, RGD1559961, CPS, Actomyosin Adenosinetriphosphatase, Formal Social Control, act 79B, Negatron, dJ393D12.2, Phosphorylations, l(3)84Ab, Negatrons, l(3)62Ca, BG:DS00004.13, Myosin, (3S)-5'-[(3-amino-3-carboxypropyl)methylsulfonio]-5'-deoxyadenosine, BEST:RE38067, Cell, dTAF230, Contractions, kettin, CAD, Social Control, beta-actin, p230, M32055, whole membrane, TAF[[II]]250/230, TFIID, Act42, ACTA3, Fast Electrons, SAM, D-titin, Taf[[II]]250, l(1)G0079, MYOHD1, PNMHH, transmembrane, MYOSIN, G Actin, TAF[[II]]230, Adenosine Triphosphatase, Acylcarnitine, negatron, Act88-F, Locomotor Activities, Resting, PYR1, act 57A, VSCM, act 5C, TAF[II]250, Actomyosin ATPase, D-Titin, Membrane, mus87E, beta, sam, alpha-Isoactin, sal, Mitochondrial Contraction, Actomyosin, Transmembrane Potential Difference, mitochondria, DmelCG17603, Physical Activities, CT41299, Act(88F), F Actin, Myohd1, l(3)S002001, DRORUD, Potentials, Resting Membrane Potential, regulation, BAP47, Membrane Potentials, ACTSG, Bap47, Actin5C, Actin-Activated, TAF1"],"pubmed_title_synonyms":["DFNA4, PNMHH, Mitochondrial, MYOSIN, Adenosine Triphosphatase, Actomyosin Adenosinetriphosphatase, OXPHOS., DFNA4A, Myosin Adenosinetriphosphatase, Contraction, NMHC-II-C, cristae, Myosin Adenosine Triphosphatase, Actin Activated ATPase, mitochondrial cristae, Myosin ATPase, Actomyosin ATPase, Myosin, Mitochondrial Contractions, Mitochondrial Contraction, Actin Activated, Contractions, Actomyosin, MYH17, ATPase, mitochondria, Adenosinetriphosphatase, myosin 1, Actin-Activated ATPase, myosin, Mitochondrion, NMHC II-C, MHC16, Actin-Activated"],"additional_accession":[]},"is_claimable":false,"name":"Myo19 Interacting Proteins IP-MS","description":"This project is aimed to detect the interacting proteins of mitochondria-tageting actin motor 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