Concept and application of circulating proteasomes.

Autor: Choi WH; BK21 FOUR Biomedical Science Program, Seoul National University College of Medicine, Seoul, 03080, Korea.; Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, 03080, Korea., Kim S; BK21 FOUR Biomedical Science Program, Seoul National University College of Medicine, Seoul, 03080, Korea.; Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, 03080, Korea.; Department of Biomedical Sciences, Seoul National University Graduate School, Seoul, 03080, Korea., Park S; Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, 03080, Korea., Lee MJ; BK21 FOUR Biomedical Science Program, Seoul National University College of Medicine, Seoul, 03080, Korea. minjlee@snu.ac.kr.; Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, 03080, Korea. minjlee@snu.ac.kr.; Department of Biomedical Sciences, Seoul National University Graduate School, Seoul, 03080, Korea. minjlee@snu.ac.kr.
Jazyk: angličtina
Zdroj: Experimental & molecular medicine [Exp Mol Med] 2021 Oct; Vol. 53 (10), pp. 1539-1546. Date of Electronic Publication: 2021 Oct 27.
DOI: 10.1038/s12276-021-00692-x
Abstrakt: Proteostasis is primarily a function of protein synthesis and degradation. Although the components and processes involved in intracellular proteostasis have been studied extensively, it is apparent that extracellular proteostasis is equitably crucial for the viability of organisms. The 26S proteasome, a unique ATP-dependent proteolytic complex in eukaryotic cells, contributes to the majority of intracellular proteolysis. Accumulating evidence suggests the presence of intact 20S proteasomes in the circulatory system (c-proteasomes), and similar to other plasma proteins, the levels of these c-proteasomes may vary, potentially reflecting specific pathophysiological conditions. Under normal conditions, the concentration of c-proteasomes has been reported to be in the range of ~0.2-2 μg/mL, which is ~2-4-fold lower than that of functional plasma proteins but markedly higher than that of signaling proteins. The characterization of c-proteasomes, such as their origin, structure, role, and clearance, has been delayed mainly due to technical limitations. In this review, we summarize the current perspectives pertaining to c-proteasomes, focusing on the methodology, including our experimental understanding. We believe that once the pathological relevance of c-proteasomes is revealed, these unique components may be utilized in the diagnosis and prognosis of diverse human diseases.
(© 2021. The Author(s).)
Databáze: MEDLINE
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