Arttamangkul S, Bhalgat M K, Haugland R P, Diwu Z, Liu J, Klaubert D H, Haugland R P
Molecular Probes, Inc., 4849 Pitchford Avenue, Eugene, Oregon 97402-9165, USA.
Anal Biochem. 1999 May 1;269(2):410-7. doi: 10.1006/abio.1999.4044.
5-(Pentafluorobenzoylamino)fluorescein (PFB-F), a new thiol-reactive molecule was synthesized to improve the detection limits and specificity of the assays for glutathione S-transferase (GST) activity and glutathione (GSH). A rapid assay method to measure GSH concentration or GST activity and the simultaneous analysis of multiple samples is possible because the glutathione adduct, GS-TFB-F, is separated from PFB-F by thin-layer chromatography (TLC) and can be quantitated by a fluorescence scanner. The detection limits for GSH and for GST activity using TLC were found to be as low as 10 pmol/microl and 1 ng/microl using equine liver GST, respectively. Determination of GSH concentration or GST activity in bovine pulmonary artery endothelial (BPAE) cell lysates gave a linear response for samples corresponding to 500-2500 cells. PFB-F could also measure GST activities of GST fusion proteins and prove to be a suitable substrate for determining the activities of human GST isozymes and other sources of mammalian GST. The selectivity of PFB-F with GSH was proven by comparing trace amount of the adducts that formed with cysteine and beta-galactosidase to that formed with GSH. The HPLC profile of a reaction mixture where cell lysate was used in place of purified GST, also shows only two main peaks, corresponding to GS-TFB-F and unreacted PFB-F. The selectivity of PFB-F for GSH was further confirmed by exposing BPAE cells to dl-buthionine-[S,R]-sulfoximine (BSO). Our results of GS-TFB-F determination indicate that 12-, 24-, or 36-h incubations with BSO caused 2-, 6-, or 7.6-fold reductions in GSH levels, respectively.
5-(五氟苯甲酰氨基)荧光素(PFB-F)是一种新的硫醇反应性分子,其合成目的是提高谷胱甘肽S-转移酶(GST)活性和谷胱甘肽(GSH)检测方法的检测限及特异性。由于谷胱甘肽加合物GS-TFB-F可通过薄层色谱(TLC)与PFB-F分离,并能用荧光扫描仪进行定量,因此能够实现一种快速测定GSH浓度或GST活性以及同时分析多个样品的方法。使用TLC时,发现马肝GST对GSH和GST活性的检测限分别低至10 pmol/微升和1 ng/微升。测定牛肺动脉内皮(BPAE)细胞裂解物中的GSH浓度或GST活性时,对应于500 - 2500个细胞的样品呈现线性响应。PFB-F还可测量GST融合蛋白的GST活性,并被证明是测定人GST同工酶及其他哺乳动物GST来源活性的合适底物。通过比较与半胱氨酸和β-半乳糖苷酶形成的加合物与与GSH形成的加合物的痕量,证明了PFB-F对GSH的选择性。使用细胞裂解物代替纯化的GST的反应混合物的高效液相色谱图谱也仅显示两个主峰,分别对应于GS-TFB-F和未反应的PFB-F。通过将BPAE细胞暴露于dl-丁硫氨酸-[S,R]-亚砜亚胺(BSO),进一步证实了PFB-F对GSH的选择性。我们对GS-TFB-F的测定结果表明,与BSO孵育12、24或三十六小时分别导致GSH水平降低2、6或7.6倍。