Msr-blue
目录号 : GC61553Msr-blue是首个"Turn-on"型的甲硫氨酸亚砜还原酶(methioninesulfoxidereductase)荧光探针,具有超过100倍的荧光增量。Msr-blue用于监测活细胞中甲硫氨酸亚砜还原酶的活性(Λex=340nm,Λem=440nm)。
Cas No.:2966537-39-1
Sample solution is provided at 25 µL, 10mM.
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Msr-blue is a first turn-on fluorescent probe for methionine sulfoxide reductase with a more than 100-fold fluorescence increment. Msr-blue is used for monitoring the enzyme activity in live cells (Λex=340 nm, Λem=440 nm)[1].
Msr-blue is emited blue fluorescence after activation by methionine sulfoxide reductase A (Msr A). Msr-blue responded to Msr A in both a time- and dose-dependent manner, and more than a 100-fold increase in the emission is observed. Msr-blue is converted to its corresponding sulfide (15′) under catalysis by either the purified Msr A or a cell lysate[1]. The 6-OHDA-treated PC12 cells as a cellular model of Parkinson's disease (PD) is employed and applied Msr-blue to probe the function of Msrs in the cells. With the aid of Msr-blue, a decline of the Msr activity in a PD model was disclosed for the first time[1].
[1]. Liangwei Zhang, et al. A specific fluorescent probe reveals compromised activity of methionine sulfoxide reductases in Parkinson's disease. Chem Sci. 2017 Apr 1;8(4):2966-2972.
Cas No. | 2966537-39-1 | SDF | |
Canonical SMILES | CC(C1=CC=C(C=C1O2)S(C)=O)=CC2=O | ||
分子式 | C11H10O3S | 分子量 | 222.26 |
溶解度 | DMSO : 25 mg/mL (112.48 mM; Need ultrasonic) | 储存条件 | Store at -20°C |
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1 mM | 4.4992 mL | 22.4962 mL | 44.9924 mL |
5 mM | 0.8998 mL | 4.4992 mL | 8.9985 mL |
10 mM | 0.4499 mL | 2.2496 mL | 4.4992 mL |
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A specific fluorescent probe reveals compromised activity of methionine sulfoxide reductases in Parkinson's disease
Chem Sci 2017 Apr 1;8(4):2966-2972.PMID:28451363DOI:PMC5382841
Oxidation of methionine residues to methionine sulfoxide (MetSO) may cause changes in protein structure and function, and may eventually lead to cell damage. Methionine sulfoxide reductases (Msrs) are the only known enzymes that catalyze the reduction of MetSO back to methionine by taking reducing equivalents from the thioredoxin system, and thus protect cells from oxidative damage. Nonetheless, a lack of convenient assays for the enzymes hampers the exploration of their functions. We report the discovery of Msr-blue, the first turn-on fluorescent probe for Msr with a >100-fold fluorescence increment from screening a rationally-designed small library. Intensive studies demonstrated the specific reduction of Msr-blue by the enzymes. Msr-blue is ready to determine Msr activity in biological samples and live cells. Importantly, we disclosed a decline of Msr activity in a Parkinson's model, thus providing a mechanistic linkage between the loss of function of Msrs and the development of neurodegeneration. The strategy for the discovery of Msr-blue would also provide guidance for developing novel probes with longer excitation/emission wavelengths and specific probes for Msr isoforms.