Byung-Chun Lee
Korea University · Biochemistry, Genetics and Molecular Biology
About the Lab
Professor Byung-Chun Lee's research lab focuses on the molecular mechanisms of redox regulation in aging, metabolic health, and stress responses, with a central emphasis on selenium biology and selenoproteins. The lab investigates how selenoproteins—particularly those with oxidoreductase functions—maintain cellular redox homeostasis and protect against oxidative damage in conditions such as osteoarthritis and age-related degeneration. Additional research explores the role of post-translational modifications, including methionine oxidation and reduction by selenoproteins like MsrB1, in regulating cytoskeletal dynamics and cellular signaling. The lab also examines the broader implications of micronutrient metabolism, such as selenium's role in mitigating trace element toxicity in plants and its potential in nutritional interventions for healthy aging.
Research Overview
Research Output Trend
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Selected Papers
15Selenium is a vital trace element present as selenocysteine (Sec) in proteins that are, thus, known as selenoproteins. Humans have 25 selenoproteins, most of which are functionally characterized as oxidoreductases, where the Sec residue plays a catalytic role in redox regulation and antioxidant activity. Glutathione peroxidase plays a pivotal role in scavenging and inactivating hydrogen and lipid peroxides, whereas thioredoxin reductase reduces oxidized thioredoxins as well as non-disulfide subs
Aging and mechanical overload are prominent risk factors for osteoarthritis (OA), which lead to an imbalance in redox homeostasis. The resulting state of oxidative stress drives the pathological transition of chondrocytes during OA development. However, the specific molecular pathways involved in disrupting chondrocyte redox homeostasis remain unclear. Here, we show that selenophosphate synthetase 1 (SEPHS1) expression is downregulated in human and mouse OA cartilage. SEPHS1 downregulation impai
Dietary restriction (DR) without malnutrition is associated with longevity in various organisms. However, it has also been shown that reduced calorie intake is often ineffective in extending life span. Selecting optimal dietary regimens for DR studies is complicated, as the same regimen may lead to different outcomes depending on genotype and environmental factors. Recent studies suggested that interventions such as moderate protein restriction with or without adequate nutrition (e.g., particula
SIGNIFICANCE: Protein structure and function can be regulated via post-translational modifications by numerous enzymatic and nonenzymatic mechanisms. Regulation involving oxidation of sulfur-containing residues emerged as a key mechanism of redox control. Unraveling the participants and principles of such regulation is necessary for understanding the biological significance of redox control of cellular processes. RECENT ADVANCES: Reversible oxidation of methionine residues by monooxygenases of t
Selenium (Se) is an essential micronutrient for humans and animals and can have beneficial effects on plants. A low concentration of Se can improve plant growth; however, high concentrations can be toxic for plants. In addition, Se can counteract stresses from toxic trace elements in plants. Hence, improved knowledge of the mechanisms involved may contribute to more effective management of Se for reducing trace element stress in plants. Here, the mechanisms of Se-mediated reduction of trace elem
The purpose of this study is to empirically examine the effect of gamification on tourist psychological outcome and knowledge gain in the context of cultural heritage sites, which are popular cruise tourism destinations. A comprehensive literature review revealed the critical role of gamification in facilitating psychological (enjoyment, flow experience, and loyalty) and behavioral outcomes (knowledge gain) at cultural heritage sites. Using a field experiment, this study employed a gamified app
Post-translational redox modification of methionine residues often triggers a change in protein function. Emerging evidence points to this reversible protein modification being an important regulatory mechanism under various physiological conditions. Reduction of oxidized methionine residues is catalyzed by methionine sulfoxide reductases (Msrs). Here, we show that one of these enzymes, a selenium-containing MsrB1, is highly expressed in immune-activated macrophages and contributes to shaping ce
Numerous secreted virulence factors have been proposed to account for the fulminating and destructive nature of Vibrio vulnificus infections. A mutant of V. vulnificus that exhibited less cytotoxicity to INT-407 human intestinal epithelial cells was screened from a library of mutants constructed by random transposon mutagenesis. A transposon-tagging method was used to identify and clone an open reading frame encoding an RTX toxin secretion ATP binding protein, RtxE, from V. vulnificus. The deduc
Methionine is an essential amino acid in mammals at the junction of methylation, protein synthesis, and sulfur pathways. However, this amino acid is highly susceptible to oxidation, resulting in a mixture of methionine-S-sulfoxide and methionine-R-sulfoxide. Whether methionine is quantitatively regenerated from these compounds is unknown. Here we report that SK-Hep1 hepatocytes grew on methionine-S-sulfoxide and consumed this compound by import and methionine-S-sulfoxide reductase (MsrA)-depende
Research Areas
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