Spatial Proteomic Approach to Characterize Skeletal Muscle Myofibers

被引:9
|
作者
Fomchenko, Katherine M. [1 ]
Walsh, Elise M. [1 ]
Yang, Xiaoping [1 ]
Verma, Rohan X. [1 ]
Lin, Brian L. [2 ]
Nieuwenhuis, Tim O. [1 ]
Patil, Arun H. [1 ]
Fox-Talbot, Karen [1 ]
McCall, Matthew N. [3 ]
Kass, David A. [2 ]
Rosenberg, Avi Z. [1 ]
Halushka, Marc K. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Dept Med, Div Cardiol, Sch Med, Baltimore, MD 21205 USA
[3] Univ Rochester, Dept Biostat & Computat Biol, Med Ctr, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
Human Protein Atlas; proteomics; skeletal muscle; twitch; SLOW;
D O I
10.1021/acs.jproteome.0c00673
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Skeletal muscle myofibers have differential protein expression resulting in functionally distinct slow- and fast-twitch types. While certain protein classes are well-characterized, the depth of all proteins involved in this process is unknown. We utilized the Human Protein Atlas (HPA) and the HPASubC tool to classify mosaic expression patterns of staining across 49,600 unique tissue microarray (TMA) images using a visual proteomic approach. We identified 2164 proteins with potential mosaic expression, of which 1605 were categorized as "likely" or "real." This list included both well-known fiber-type-specific and novel proteins. A comparison of the 1605 mosaic proteins with a mass spectrometry (MS)-derived proteomic dataset of single human muscle fibers led to the assignment of 111 proteins to fiber types. We additionally used a multiplexed immunohistochemistry approach, a multiplexed RNA-ISH approach, and STRING v11 to further assign or suggest fiber types of newly characterized mosaic proteins. This visual proteomic analysis of mature skeletal muscle myofibers greatly expands the known repertoire of twitch-type-specific proteins.
引用
收藏
页码:888 / 894
页数:7
相关论文
共 50 条
  • [21] Proteomic analysis of bovine skeletal muscle hypertrophy
    Bouley, J
    Meunier, B
    Chambon, C
    De Smet, S
    Hocquette, JF
    Picard, B
    PROTEOMICS, 2005, 5 (02) : 490 - 500
  • [22] Biochemical and proteomic profiling of diabetic skeletal muscle
    Mullen, Edel
    Ohlendieck, Kay
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2009, 24 : S6 - S6
  • [23] Proteomic responses of skeletal and cardiac muscle to exercise
    Burniston, Jatin G.
    Hoffman, Eric P.
    EXPERT REVIEW OF PROTEOMICS, 2011, 8 (03) : 361 - 377
  • [24] Proteomic identification of biomarkers of skeletal muscle disorders
    Ohlendieck, Kay
    BIOMARKERS IN MEDICINE, 2013, 7 (01) : 169 - 186
  • [25] Proteomic approach to characterize biochemistry of meat quality defects
    Schilling, M. W.
    Suman, S. P.
    Zhang, X.
    Nair, M. N.
    Desai, M. A.
    Cai, K.
    Ciaramella, M. A.
    Allen, P. J.
    MEAT SCIENCE, 2017, 132 : 131 - 138
  • [26] Current Methodologies for Inducing Aligned Myofibers in Tissue Constructs for Skeletal Muscle Tissue Regeneration
    Sicherer, Sydnee T.
    Haque, Noor
    Parikh, Yash
    Grasman, Jonathan M.
    ADVANCES IN WOUND CARE, 2025, 14 (02) : 114 - 131
  • [27] Classification of myofibers using statistics of the helix angle: a novel approach to characterize the structure of the human heart
    Mekkaoui C.
    Huang S.
    Dai G.
    Reese T.G.
    Thiagalingham A.
    Hoffmann U.
    Jackowski M.P.
    Sosnovik D.E.
    Journal of Cardiovascular Magnetic Resonance, 13 (Suppl 1)
  • [28] Skeletal Muscle Myofibers Directly Contribute to LPS-Induced Systemic Inflammatory Tone
    Bivona, Joseph J., III
    Mank, Madeleine M.
    Stapleton, Renee D.
    Files, D. Clark
    Toth, Michael J.
    Poynter, Matthew E.
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [29] Optimization of a proteomic approach for evidencing and identifying oxidized proteins during human skeletal muscle aging
    Santos, S.
    Baraibar, M.
    Le Boulch, M.
    Larsson, L.
    Friguet, B.
    EXPERIMENTAL GERONTOLOGY, 2013, 48 (07) : 687 - 688
  • [30] PEROXISOMES IN REGENERATING HUMAN SKELETAL MYOFIBERS
    WAKAYAMA, Y
    ACTA ANATOMICA, 1989, 136 (02): : 121 - 124