enzyme

RNA-mediated modulation of cell metabolism

RNA-mediated modulation of cell metabolism

The perception of RNA–protein interactions is currently changing from a protein-centric approach, in which proteins regulate the expression and activity of RNA, to a more complex view, in which RNA molecules can directly regulate protein's function and thus cell behavior, in a process called riboregulation.

Nitric oxide does not inhibit but is metabolized by the cytochrome bcc-aa3 supercomplex

Nitric oxide (NO) is a well-known active site ligand and inhibitor of respiratory terminal oxidases. Here, we investigated the interaction of NO with a purified chimeric bcc-aa3 supercomplex composed of Mycobacterium tuberculosis cytochrome bcc and Mycobacterium smegmatis aa3-type terminal oxidase. Strikingly, we found that the enzyme in turnover with O2 and reductants is resistant to inhibition by the ligand, being able to metabolize NO at 25◦C with an apparent turnover number as high as ≈303 mol NO (mol enzyme)−1 min−1 at 30 µM NO.

Screening pyridine derivatives against human hydrogen sulfide-synthesizing enzymes by orthogonal methods

Biosynthesis of hydrogen sulfide (H2S), a key signalling molecule in human (patho)physiology, is mostly accomplished by the human enzymes cystathionine β-synthase (CBS), cystathionine γ-lyase (CSE) and 3-mercaptopyruvate sulfurtransferase (MST). Several lines of evidence have shown a close correlation between increased H2S production and human diseases, such as several cancer types and amyotrophic lateral sclerosis. Identifying compounds selectively and potently inhibiting the human H2S-synthesizing enzymes may therefore prove beneficial for pharmacological applications.

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