Engstler M, Talhouk J W, Smith R E, Schauer R
Biochemisches Institut, Christian-Albrechts-Universität, Kiel, Germany.
Anal Biochem. 1997 Aug 1;250(2):176-80. doi: 10.1006/abio.1997.2205.
When compared to bacterial or viral sialidases, eukaryotic sialidases are expressed at lower levels and frequently show poor specific activities. The identification and characterization of sialidases from eukaryotes have been slowed down due to the limited sensitivity of available sialidase substrates. Therefore, we chemically synthesized a fluorogenic compound, 4-trifluoromethylumbelliferyl-alpha-D-N-acetylneuraminic acid (CF3MU-Neu5Ac), and tested its use as a substrate for eight different sialidases, including enzymes from viral, bacterial, and eukaryotic sources. Kinetic analysis revealed CF3MU-Neu5Ac to be a very sensitive sialidase substrate. Furthermore, this substance proves to be perfectly suitable for the in vivo examination of sialidases and for the detection of recombinant sialidase by means of expression cloning.
与细菌或病毒唾液酸酶相比,真核生物唾液酸酶的表达水平较低,且常常表现出较低的比活性。由于现有唾液酸酶底物的灵敏度有限,真核生物唾液酸酶的鉴定和特性研究进展缓慢。因此,我们化学合成了一种荧光化合物,4-三氟甲基伞形酮基-α-D-N-乙酰神经氨酸(CF3MU-Neu5Ac),并测试了它作为八种不同唾液酸酶底物的用途,这些唾液酸酶包括来自病毒、细菌和真核生物来源的酶。动力学分析表明CF3MU-Neu5Ac是一种非常灵敏的唾液酸酶底物。此外,该物质被证明完全适用于唾液酸酶的体内检测以及通过表达克隆检测重组唾液酸酶。