1-磷酸鞘氨醇转运蛋白同源物2(Spns2)抑制剂的测定。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yugesh Kharel , Tao Huang , Webster L. Santos , Kevin R. Lynch
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引用次数: 1

摘要

鞘氨醇-1-磷酸(S1P)途径仍然是药物发现的活跃研究领域,因为S1P调节剂是治疗自身免疫性疾病(如多发性硬化症和溃疡性结肠炎)的有效药物。因此,可以探测通路中的其他节点以寻找替代的候选治疗方法。由于S1P以“外-内”的方式激发其功能,靶向受体上游的转运蛋白Spns2引起了极大的兴趣。为了支持我们抑制S1P转运的药物化学活动,我们开发了一种基于哺乳动物细胞的检测方法。在该方案中,通过用抑制剂处理HeLa、U-937和THP-1细胞来评估Spns2的抑制作用,并通过LC-MS/MS定量在细胞外环境中输出的S1P。我们的研究表明,培养基中S1P的含量与抑制剂浓度成反比。我们的调查细节如下所述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assay of Sphingosine 1-phosphate Transporter Spinster Homolog 2 (Spns2) Inhibitors

The sphingosine-1-phosphate (S1P) pathway remains an active area of research for drug discovery because S1P modulators are effective medicine for autoimmune diseases such as multiple sclerosis and ulcerative colitis. As such, other nodes in the pathway can be probed for alternative therapeutic candidates. As S1P elicits its function in an ‘outside-in’ fashion, targeting the transporter, Spns2, which is upstream of the receptors, is of great interest. To support our medicinal chemistry campaign to inhibit S1P transport, we developed a mammalian cell-based assay. In this protocol, Spns2 inhibition is assessed by treating HeLa, U-937, and THP-1 cells with inhibitors and S1P exported in the extracellular milieu is quantified by LC-MS/MS. Our studies demonstrated that the amount of S1P in the media in inversely proportional to inhibitor concentration. The details of our investigations are described herein.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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