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Related Concept Videos

Proteomics01:33

Proteomics

8.7K
A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term...
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Temporomandibular Joint Pain Measurement by Bite Force and Von Frey Filament Assays in Mice
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Proteomic Expression Profile in Human Temporomandibular Joint Dysfunction.

Andrea Duarte Doetzer1, Roberto Hirochi Herai1, Marília Afonso Rabelo Buzalaf2

  • 1Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba 80215-901, Brazil.

Diagnostics (Basel, Switzerland)
|April 3, 2021
PubMed
Summary

This study analyzed protein expression in temporomandibular joint dysfunction (TMD) patients. Different protein profiles were found in anterior disc displacement without reduction, condylar hyperplasia, and mandibular dislocation, aiding targeted treatment.

Keywords:
protein expressiontemporomandibular jointtemporomandibular joint dysfunction

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Area of Science:

  • Biochemistry
  • Proteomics
  • Oral and Maxillofacial Surgery

Background:

  • Temporomandibular joint dysfunction (TMD) is a complex, multifactorial condition impacting quality of life.
  • Common TMD types include anterior disc displacement without reduction (DDWoR), condylar hyperplasia (CH), and mandibular dislocation (MD).
  • The precise etiology and distinct pathological mechanisms of these TMD subtypes remain incompletely understood.

Purpose of the Study:

  • To investigate and compare the proteomic profiles of synovial fluid and temporomandibular joint disc tissue.
  • To identify specific protein expression differences among patients with DDWoR, CH, and MD.
  • To enhance the understanding of the molecular basis underlying different TMD pathologies.

Main Methods:

  • Proteomic analysis using label-free nLC-MS/MS on synovial fluid and joint disc samples.
  • Collection of samples from nine patients diagnosed with DDWoR (n=3), CH (n=4), and MD (n=2).
  • Bioinformatics analysis for protein identification and functional annotation.

Main Results:

  • Distinct protein expression profiles were observed across the three TMD conditions.
  • Novel proteins were identified in both synovial fluid and temporomandibular joint disc samples.
  • The findings highlight molecular differences between DDWoR, CH, and MD.

Conclusions:

  • The proteomic analysis reveals unique molecular signatures for different TMD subtypes.
  • Identifying these proteins offers insights into the pathogenesis and progression of specific TMDs.
  • This research may facilitate the development of more targeted and effective treatment strategies for TMD patients.