Isolation and purification of high molecular weight adiponectin from human plasma fraction

•Adiponectin represents a potential therapeutic target for metabolic diseases.•Challenges in producing high molecular weight (HMW) adiponectin have hindered clinical translation.•We proposed a method capable of isolating and purifying biologically active human HMW adiponectin from discarded plasma f...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2024-05, Vol.1238, p.124111-124111, Article 124111
Hauptverfasser: Hyun Boo, Kyung, Woo Kim, Jin, Song, Minkyung
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Sprache:eng
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Zusammenfassung:•Adiponectin represents a potential therapeutic target for metabolic diseases.•Challenges in producing high molecular weight (HMW) adiponectin have hindered clinical translation.•We proposed a method capable of isolating and purifying biologically active human HMW adiponectin from discarded plasma fractions. Adiponectin, a crucial protein hormone originating from adipose tissue, regulates key metabolic processes, including lipid metabolism, mitochondrial activity, and insulin sensitivity. These pleiotropic roles of adiponectin, along with its inverse correlation with metabolic disorders such as obesity, type II diabetes, and atherosclerosis, establish this protein as a potential therapeutic target. However, due to this complexity, challenges have arisen in its production with a natural conformation in bacterial or mammalian expression systems, hindering clinical translation. Furthermore, while inducers for adiponectin secretion or chemical agonists targeting adiponectin receptors have shown promise in laboratory settings, clinical studies with these agents have not yet been conducted. This study proposes a method for isolating and purifying natural high molecular weight (HMW) adiponectin from discarded plasma fractions during the conventional pharmaceutical protein manufacturing process. The process involved Cohn-Oncley fractionation, initial chromatography using reduced cellufine formyl, and subsequent purification via DEAE Sepharose chromatography. Characterization involved gel electrophoresis and biological assays on a hepatocyte cell-line. The purification process effectively captured adiponectin from the I + III paste, demonstrating that this fraction contained a significant portion of total plasma adiponectin. The two-step chromatography led to highly purified HMW adiponectin, confirmed by native-PAGE showing a 780 kDa multimeric complex. Biological assessments demonstrated normal downstream signaling, with HMW adiponectin inducing AMPK phosphorylation. This study demonstrates the feasibility of obtaining purified HMW adiponectin by repurposing plasma fractionation processes. It offers a promising avenue for the HMW adiponectin production, tapping into HMW adiponectin’s therapeutic potential against metabolic disorders while optimizing plasma resource utilization in healthcare.
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2024.124111