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通过定点诱变鉴定激素敏感性脂肪酶的活性位点丝氨酸

Identification of the active site serine of hormone-sensitive lipase by site-directed mutagenesis.

作者信息

Holm C, Davis R C, Osterlund T, Schotz M C, Fredrikson G

机构信息

Department of Medical and Physiological Chemistry, Lund University, Sweden.

出版信息

FEBS Lett. 1994 May 16;344(2-3):234-8. doi: 10.1016/0014-5793(94)00403-x.

Abstract

The consensus pentapeptide GXSXG is found in virtually all lipases/esterases and generally contains the active site serine. The primary sequence of hormone-sensitive lipase contains a single copy of this pentapeptide, surrounding Ser-423. We have analyzed the catalytic role of Ser-423 by site-directed mutagenesis and expression of the mutant hormone-sensitive lipase in COS cells. Substitution of Ser-423 by several different amino acids resulted in the complete abolition of both lipase and esterase activity, whereas mutation of other conserved serine residues had no effect on the catalytic activity. These results strongly suggest that Ser-423 is the active site serine of hormone-sensitive lipase.

摘要

共有五肽GXSXG几乎存在于所有脂肪酶/酯酶中,且通常包含活性位点丝氨酸。激素敏感性脂肪酶的一级序列含有该五肽的单拷贝,围绕着丝氨酸423。我们通过定点诱变以及在COS细胞中表达突变型激素敏感性脂肪酶,分析了丝氨酸423的催化作用。用几种不同氨基酸取代丝氨酸423导致脂肪酶和酯酶活性完全丧失,而其他保守丝氨酸残基的突变对催化活性没有影响。这些结果有力地表明,丝氨酸423是激素敏感性脂肪酶的活性位点丝氨酸。

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