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激素原转化酶2对脑啡肽原及脑啡肽原相关底物的特异性

Specificity of prohormone convertase 2 on proenkephalin and proenkephalin-related substrates.

作者信息

Johanning K, Juliano M A, Juliano L, Lazure C, Lamango N S, Steiner D F, Lindberg I

机构信息

Department of Biochemistry and Molecular Biology, Louisiana State University Medical Center, School of Medicine, New Orleans, Louisiana 70112, USA.

出版信息

J Biol Chem. 1998 Aug 28;273(35):22672-80. doi: 10.1074/jbc.273.35.22672.

Abstract

In the central and peripheral nervous systems, the neuropeptide precursor proenkephalin must be endoproteolytically cleaved by enzymes known as prohormone convertases 1 and 2 (PC1 and PC2) to generate opioid-active enkephalins. In this study, we have investigated the specificity of recombinant mouse PC2 for proenkephalin-related internally quenched (IQ) peptides, for methylcoumarin amide-based fluorogenic peptides, and for recombinant rat proenkephalin. IQ peptides exhibited specificity constants (kcat/Km) between 9.4 x 10(4) M-1 s-1 (Abz-Val-Pro-Arg-Met-Glu-Lys-Arg-Tyr-Gly-Gly-Phe-Met-Gln-EDDnp+ ++; where Abz is ortho-aminobenzoic acid and EDDnp is N-(2, 4-dinitrophenyl)ethylenediamine)) and 0.24 x 10(4) M-1 s-1 (Abz-Tyr-Gly-Gly-Phe-Met-Arg-Arg-Val-Gly-Arg-Pro-Glu-EDDnp), with the peptide B to Met-enk-Arg-Phe cleavage preferred (Met-enk is met-enkephalin). Fluorogenic substrates with P1, P2, and P4 basic amino acids were hydrolyzed with specificity constants ranging between 2.0 x 10(3) M-1 s-1 (Ac-Orn-Ser-Lys-Arg-MCA; where MCA is methylcoumarin amide) and 1.8 x 10(4) M-1 s-1 (<Glu-Arg-Thr-Lys-Arg-MCA; where <Glu is pyroglutamic acid). Substrates containing only a single basic residue were not appreciably hydrolyzed, and substrates lacking a P4 Arg exhibited kcat of less than 0.05 s-1. Substitution of ornithine for Lys at the P4 position did not significantly affect the kcat but increased the Km 2-fold. Data from both sets of fluorogenic substrates supported the contribution of a P4 Arg to PC2 preference. Analysis of proenkephalin reaction products using immunoblotting and gel permeation chromatography demonstrated that PC2 can directly cleave proenkephalin and that the generation of small opioid peptides from intermediates is mediated almost entirely by PC2 rather than by PC1. These results are in accord with the analysis of PC2 knock-out brains, in which the amounts of three mature enkephalins were depleted by more than three-quarters.

摘要

在中枢和外周神经系统中,神经肽前体脑啡肽原必须被称为激素原转化酶1和2(PC1和PC2)的酶进行内蛋白水解切割,以生成具有阿片样活性的脑啡肽。在本研究中,我们研究了重组小鼠PC2对与脑啡肽原相关的内部淬灭(IQ)肽、基于甲基香豆素酰胺的荧光肽以及重组大鼠脑啡肽原的特异性。IQ肽的特异性常数(kcat/Km)在9.4×10⁴ M⁻¹ s⁻¹(Abz-Val-Pro-Arg-Met-Glu-Lys-Arg-Tyr-Gly-Gly-Phe-Met-Gln-EDDnp;其中Abz是邻氨基苯甲酸,EDDnp是N-(2,4-二硝基苯基)乙二胺)和0.24×10⁴ M⁻¹ s⁻¹(Abz-Tyr-Gly-Gly-Phe-Met-Arg-Arg-Val-Gly-Arg-Pro-Glu-EDDnp)之间,其中肽B至甲硫脑啡肽-精氨酸-苯丙氨酸的切割更受青睐(甲硫脑啡肽是甲硫脑啡肽)。具有P1、P2和P4碱性氨基酸的荧光底物以2.0×10³ M⁻¹ s⁻¹(Ac-Orn-Ser-Lys-Arg-MCA;其中MCA是甲基香豆素酰胺)至1.8×10⁴ M⁻¹ s⁻¹(<Glu-Arg-Thr-Lys-Arg-MCA;其中<Glu是焦谷氨酸)的特异性常数进行水解。仅含有单个碱性残基的底物未被明显水解,而缺乏P4精氨酸的底物的kcat小于0.05 s⁻¹。在P4位置用鸟氨酸取代赖氨酸对kcat没有显著影响,但使Km增加了2倍。两组荧光底物的数据都支持P4精氨酸对PC2偏好性的贡献。使用免疫印迹和凝胶渗透色谱法对脑啡肽原反应产物的分析表明,PC2可以直接切割脑啡肽原,并且从小肽中间体生成小的阿片样肽几乎完全由PC2介导,而不是由PC1介导。这些结果与对PC2基因敲除小鼠脑的分析一致,在该分析中,三种成熟脑啡肽的量减少了四分之三以上。

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