Sphingosine 1-phosphate lyase enzyme assay using a BODIPY-labeled substrate

被引:25
作者
Bandhuvula, Padmavathi [1 ]
Li, Zaiguo [2 ]
Bittman, Robert [2 ]
Saba, Julie D. [1 ]
机构
[1] Childrens Hosp Oakland, Res Inst, Canc Biol Lab, Oakland, CA 94609 USA
[2] CUNY Queens Coll, Dept Chem & Biochem, Flushing, NY 11367 USA
基金
美国国家卫生研究院;
关键词
Sphingosine 1-phosphate lyase; Sphingosine; 1-phosphate; BODIPY; Fluorescent; Sphingolipid; NBD; Assay; FLUORESCENCE DETECTION METHOD; SPHINGOSINE-1-PHOSPHATE LYASE; SPHINGOLIPID METABOLISM; 1ST SYNTHESIS; CHOLESTEROL; DERIVATIVES; PHOSPHOLIPIDS; CERAMIDE;
D O I
10.1016/j.bbrc.2009.01.106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Sphingosine 1-phosphate lyase (SPL) is responsible for the irreversible catabolism of sphingosine 1-phosphate, which signals through five membrane receptors to mediate cell stress responses, angiogenesis, and lymphocyte trafficking. The standard assay for SPL activity utilizes a radioactive clihydrosphingosine 1-phosphate substrate and is expensive and Cumbersome. In this study, we describe an SPL assay that employs an omega-labeled BODIPY-sphingosine 1-phosphate substrate, allowing fluorescent product detection by HPLC and incorporating advantages of the BODIPY fluorophore. The major aldehyde product is confirmed by reaction with 2,4-dinitrophenylhydrazine. The SPL-catalyzed reaction is linear over a 30 min time period and yields a K-m of 35 mu M for BODIPY-sphingosine 1-phosphate. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:366 / 370
页数:5
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