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Differential proteomic analysis of acute contusive spinal cord injury in rats using iTRAQ reagent labeling and LC-MS/MS

  • Anshu Chen
  • , Shixin Sun
  • , Rangaswamyrao Ravikumar
  • , Nishant P. Visavadiya
  • , Joe E. Springer

Producción científica: Articlerevisión exhaustiva

10 Citas (Scopus)

Resumen

In this experimental study, differential labeling with isobaric tags for relative and absolute quantitation (iTRAQ) reagents followed by liquid chromatography (LC) and tandem mass spectrometry (MS/MS) proteomic approach was used to investigate differences in the proteome of rat spinal cord at 24 h following a moderate contusion injury. Spinal cord protein samples from the injury epicenter (or from sham controls) were trypsinized and differentially labeled with iTRAQ isotopic reagents. The differentially labeled samples were then combined into one sample mixture, separated by LC, and analyzed using MS/MS. Proteins were quantified by comparing the peak areas of iTRAQ reporter fragment ions in MS/MS spectra. The outcome of this analysis revealed that proteins involved in ubiquitination, endocytosis and exocytosis, energy metabolism, inflammatory response, oxidative stress, cytoskeletal disruption, and vascular damage were significantly altered at 24 h following spinal cord injury (SCI). This study demonstrates the utility of the iTRAQ method in proteomic studies and provides further insights into secondary events that occur during acute times following SCI.

Idioma originalEnglish
Páginas (desde-hasta)2247-2255
Número de páginas9
PublicaciónNeurochemical Research
Volumen38
N.º11
DOI
EstadoPublished - nov 2013

Nota bibliográfica

Funding Information:
Acknowledgments The authors gratefully acknowledge Dr. Melanie L. McEwen for technical support. This work was supported by the Craig H. Neilsen Foundation, the Morton Cure Paralysis Foundation, and an endowment from Cardinal Hill Rehabilitation Hospital.

Financiación

Acknowledgments The authors gratefully acknowledge Dr. Melanie L. McEwen for technical support. This work was supported by the Craig H. Neilsen Foundation, the Morton Cure Paralysis Foundation, and an endowment from Cardinal Hill Rehabilitation Hospital.

Financiadores
Cardinal Hill Rehabilitation Hospital
Morton Cure Paralysis Fund
Craig H. Neilsen Foundation

    ASJC Scopus subject areas

    • Biochemistry
    • Cellular and Molecular Neuroscience

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