Article ; Online: Comprehensive Characterization of Protein Turnover by Comparative SILAC Labeling Analysis in 3T3-L1.
2023 Volume 22, Issue 6, Page(s) 1723–1733
Abstract: A balance between the synthesis and degradation of proteins is referred to as protein turnover, which is crucial for cellular protein homeostasis. Proteome-wide analysis of protein turnover in adipocytes, which are well-known for their role in energy ... ...
Abstract | A balance between the synthesis and degradation of proteins is referred to as protein turnover, which is crucial for cellular protein homeostasis. Proteome-wide analysis of protein turnover in adipocytes, which are well-known for their role in energy storage and their link to obesity and metabolism disorders, is yet to be conducted. Thus, with this objective in mind, our investigation utilized a comparative analysis of time-dependent SILAC labeling to assess protein turnover in 3T3-L1 adipocytes, spanning a period of 0 to 144 h. We observed that relatively faster or slower protein half-lives in several protein groups were associated with the PPARγ signaling pathway, energy metabolism, extracellular matrix, ubiquitin-proteasome system, RNA splicing, Golgi complex, and lysosome. It is anticipated that these protein half-life profiles will provide greater clarity on the life cycle of adipocyte proteome and shed light on how they maintain protein homeostasis. |
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MeSH term(s) | Animals ; Mice ; Proteome/genetics ; Proteome/metabolism ; 3T3-L1 Cells ; Adipocytes/metabolism ; Proteolysis ; Proteasome Endopeptidase Complex/metabolism ; Cell Differentiation |
Chemical Substances | Proteome ; Proteasome Endopeptidase Complex (EC 3.4.25.1) |
Language | English |
Publishing date | 2023-04-14 |
Publishing country | United States |
Document type | Journal Article ; Research Support, Non-U.S. Gov't |
ZDB-ID | 2078618-9 |
ISSN | 1535-3907 ; 1535-3893 |
ISSN (online) | 1535-3907 |
ISSN | 1535-3893 |
DOI | 10.1021/acs.jproteome.2c00763 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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