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Updated: May 9, 2026

15:32
Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay
Published on: August 5, 2011
The proteomics and interactomics of human erythrocytes
Steven R Goodman1, Ovidiu Daescu, David G Kakhniashvili
1Department of Biochemistry & Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA. goodmans@upstate.edu
Experimental Biology and Medicine (Maywood, N.J.)
|July 17, 2013
Summary
This review details advances in human erythrocyte proteome and interactome research since 2007. New proteomics and interactomics tools reveal critical protein changes in blood disorders like sickle cell disease.
Area of Science:
- Biochemistry
- Molecular Biology
- Hematology
Background:
- The human erythrocyte proteome and interactome are crucial for understanding red blood cell function and disease.
- Significant advancements in proteomics and interactomics have expanded our knowledge since 2007.
Purpose of the Study:
- To review recent progress in characterizing the human erythrocyte proteome and interactome.
- To highlight the application of these tools in studying blood disorders, with a focus on sickle cell disease.
Main Methods:
- Proteomics and interactomics techniques were employed to identify and analyze erythrocyte proteins.
- Comparative analyses were performed to track changes in protein profiles over time and in disease states.
Main Results:
- The number of identified unique erythrocyte proteins has increased from 751 in 2007 to 2289.
- Proteomics and interactomics have identified biomarkers for sickle cell disease severity and erythrocyte membrane alterations.
- The pharmacoproteomic effects of hydroxyurea and key protein interaction network changes in sickle cell disease were elucidated.
Conclusions:
- Proteomics and interactomics are powerful tools for advancing our understanding of erythrocyte biology and blood disorders.
- Continued research in this area holds promise for identifying novel diagnostic markers and therapeutic targets.
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