Abstract:Hydrogen sulfide (H(2)S) is a synaptic modulator as well as a neuroprotectant. Currently, pyridoxal-5'-phosphate (PLP)-dependent cystathionine beta-synthase (CBS) is thought to be the major H(2)S-producing enzyme in the brain. We recently found that brain homogenates of CBS-knockout mice, even in the absence of PLP, produce H(2)S at levels similar to those of wild-type mice, suggesting the presence of another H(2)S-producing enzyme. Here we show that 3-mercaptopyruvate sulfurtransferase (3MST) in combination w… Show more
“…Following release, hydrogen sulfide can be stored in cells as bound sulfane sulfur that can be released by reducing conditions (44). Bound sulfane sulfur is the major determinant of physiological functions of hydrogen sulfide (45)(46)(47). Recent studies indicate that hydrogen sulfide has diverse effects on cell function including cell survival, hemodynamics, and inflammation (44); however, its role in protein synthesis has not been examined in detail.…”
“…Following release, hydrogen sulfide can be stored in cells as bound sulfane sulfur that can be released by reducing conditions (44). Bound sulfane sulfur is the major determinant of physiological functions of hydrogen sulfide (45)(46)(47). Recent studies indicate that hydrogen sulfide has diverse effects on cell function including cell survival, hemodynamics, and inflammation (44); however, its role in protein synthesis has not been examined in detail.…”
“…H 2 S, or aqueous sulphide, elicits diverse physiological responses, including modulation of blood pressure and reduction of ischemia reperfusion injury [3][4][5] , exertion of anti-inflammatory effects 6 and reduction of metabolic rate 7 . The production of H 2 S is catalysed by the two pyridoxal 5′-phosphate-dependent enzymes, cystathionine β-synthase (CBS) 8 , and cystathionine γ-lyase 9 , and indirectly, via a pyridoxal 5′-phosphateindependent enzyme, 3-mercaptopyruvate sulphurtransferase 10 .…”
Aqueous sulphides, including hydrogen sulphide, have important roles in biological signalling and metabolic processes. Here we develop a selective sulphide-trapping strategy involving sulphide addition to an aldehyde; the resulting hemithioacetal undergoes a michael addition with an adjacent unsaturated acrylate ester to form a thioacetal at neutral pH in aqueous solution. Employing this new strategy, two sulphide-selective fluorescent probes, sFP-1 and sFP-2, were synthesized on the basis of two different fluorophore templates. These probes exhibit an excellent fluorescence increase and an emission maximum shift (sFP-1) in response to na 2 s and H 2 s in a high thiol background as found under physiological conditions. We show the utility of the probes for the selective detection of sulphides, and the capacity of our probes to monitor enzymatic H 2 s biogenesis and image free sulphide in living cells.
“…Hydrogen sulfide (H 2 S) is synthesized by three enzymes: cystathionine -synthase (CBS), 2 cystathionine ␥-lyase (CSE), and 3-mercaptopyruvate sulfurtransferase (3MST) along with cysteine aminotransferase (CAT) (1)(2)(3)(4)(5)(6). 3MST produces H 2 S from 3-mercaptopyruvate (3MP), which is produced from cysteine and ␣-ketoglutarate (␣-KG) by CAT that is identical with aspartate aminotransferase (4,7,8).…”
mentioning
confidence: 99%
“…3MST produces H 2 S from 3-mercaptopyruvate (3MP), which is produced from cysteine and ␣-ketoglutarate (␣-KG) by CAT that is identical with aspartate aminotransferase (4,7,8). In the central nervous system, CBS is mainly localized to astrocytes, and 3MST to neurons (4,9,10).…”
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