Proteomic identification of altered proteins in skeletal muscle during chronic potassium depletion: Implications for hypokalemic myopathy

J Proteome Res. 2006 Dec;5(12):3326-35. doi: 10.1021/pr060136h.

Abstract

Prolonged potassium depletion is a well-known cause of myopathy. The pathophysiology of hypokalemic myopathy, however, remains unclear. We performed a gel-based, differential proteomics study to define altered proteins in skeletal muscles during chronic potassium depletion. BALB/c mice were fed with normal chow (0.36% K+) or K+-depleted (KD) diet (<0.001% K+) for 8 weeks (n = 5 in each group). Left gastrocnemius muscles were surgically removed from each animal. Histopathological examination showed mild-degree infiltration of polymornuclear and mononuclear cells at the interstitium of the KD muscles. Extracted proteins were resolved with two-dimensional electrophoresis (2-DE), and visualized with Coomassie Brilliant Blue R-250 stain. Quantitative intensity analysis revealed 16 up-regulated protein spots in the KD muscles, as compared to the controls. These differentially expressed proteins were subsequently identified by peptide mass fingerprinting and by quadrupole time-of-flight tandem mass spectrometry (Q-TOF MS/MS). Most of the altered proteins induced by chronic potassium depletion were muscle enzymes that play significant roles in several various metabolic pathways. Other up-regulated proteins included myosin-binding protein H, alpha-B Crystallin, and translationally controlled tumor protein (TCTP). These findings may lead to a new roadmap for research on hypokalemic myopathy, to better understanding of the pathophysiology of this medical disease, and to biomarker discovery.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blotting, Western
  • Electrophoresis, Gel, Two-Dimensional
  • Gene Expression Regulation*
  • Hypokalemic Periodic Paralysis / metabolism*
  • Male
  • Mass Spectrometry
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Muscle, Skeletal / metabolism*
  • Peptide Mapping
  • Potassium Deficiency / metabolism*
  • Proteins / genetics
  • Proteins / metabolism*
  • Proteomics
  • Sequence Analysis, DNA
  • Tumor Protein, Translationally-Controlled 1

Substances

  • Proteins
  • Tpt1 protein, mouse
  • Tumor Protein, Translationally-Controlled 1