Free amino acids accelerate the time-dependent inactivation of rat liver nucleotide pyrophosphatase/phosphodiesterase Enpp3 elicited by EDTA

IF 3 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Amino Acids Pub Date : 2024-12-06 DOI:10.1007/s00726-024-03431-4
Ana Romero, Guadalupe Cumplido-Laso, Ascensión Fernández, Javier Moreno, José Canales, Rui Ferreira, Juan López-Gómez, João Meireles Ribeiro, María Jesús Costas, José Carlos Cameselle
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Abstract

Nucleotide-pyrophosphatases/phosphodiesterases (NPP/PDE) are membrane or secreted Zn2+-metallohydrolases of nucleoside-5´-monophosphate derivatives. They hydrolyze, for instance, ATP and 4-nitrophenyl-dTMP, and belong to the ecto-nucleotide pyrophosphatase/phosphodiesterase (ENPP) family that contains seven members (ENPP1-ENPP7). Earlier we had shown that an NPP/PDE activity solubilized and partially purified from rat liver membranes is inactivated by EDTA in a time-dependent fashion, an effect enhanced by glycine and blocked by the 4-nitrophenyl-dTMP. Here, we extended this observation to other free amino acids. Activity assays started after different incubation lengths with EDTA provided first-order, apparent inactivation constants (ki(ap)). With the exception of cysteine (a strong inhibitor) and histidine (itself evoking a time-dependent inactivation), free amino acids themselves did not affect activity but increased ki(ap). The results are compatible with a conformational change of NPP/PDE evoked by interaction with free amino acids. The enzyme preparation was analyzed to identify what ENPP family members were present. First, the hydrolytic activity on 2´,3´-cGAMP was assayed because until very recently ENPP1 was the only mammalian enzyme known to display it. 2´,3´-cGAMP hydrolase activity was clearly detected, but mass spectrometry data obtained by LC-MS/MS gave evidence that only rat Enpp3, Enpp4 and Enpp5 were present with low abundance. This finding coincided in time with a recent publication claiming that mouse Enpp3 hydrolyzes 2´,3´-cGAMP, and that Enpp1 and Enpp3 account for all the 2´,3´-cGAMP hydrolase activity in mice. So, our results are confirmatory of Enpp3 activity towards 2´,3´-cGAMP. Finally, the effect of amino acids could be relevant to NPP/PDE actions dependent on protein-protein interactions, like the known insulin-related effects of ENPP1 and possibly ENPP3.

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游离氨基酸加速了EDTA诱导的大鼠肝脏核苷酸焦磷酸酶/磷酸二酯酶Enpp3的时间依赖性失活。
核苷酸焦磷酸酶/磷酸二酯酶(NPP/PDE)是核苷-5′-单磷酸衍生物的膜或分泌的Zn2+-金属水解酶。例如,它们水解ATP和4-硝基苯基- dtmp,并且属于包含7个成员(ENPP1-ENPP7)的外核苷酸焦磷酸酶/磷酸二酯酶(ENPP)家族。先前我们已经证明,从大鼠肝膜中溶解和部分纯化的NPP/PDE活性被EDTA以一种时间依赖性的方式灭活,甘氨酸增强了这种作用,并被4-硝基苯基- dtmp阻断。在这里,我们将这一观察扩展到其他游离氨基酸。不同EDTA孵育时间后开始的活性测定提供了一级表观失活常数(ki(ap))。除了半胱氨酸(一种强抑制剂)和组氨酸(本身引起时间依赖性失活)外,游离氨基酸本身不影响活性,但增加了ki(ap)。结果与NPP/PDE与游离氨基酸相互作用引起的构象变化相一致。对酶制剂进行分析以确定ENPP家族成员的存在。首先,测定了2´,3´-cGAMP的水解活性,因为直到最近,ENPP1是唯一已知的具有这种水解活性的哺乳动物酶。2´,3´-cGAMP水解酶活性明显,但LC-MS/MS质谱数据显示,只有大鼠的Enpp3、Enpp4和Enpp5存在低丰度。这一发现与最近发表的一篇文章一致,该论文声称小鼠Enpp3可以水解2´,3´-cGAMP,并且Enpp1和Enpp3可以解释小鼠所有的2´,3´-cGAMP水解酶活性。因此,我们的结果证实了Enpp3对2´,3´-cGAMP的活性。最后,氨基酸的作用可能与依赖于蛋白质相互作用的NPP/PDE作用有关,如已知的ENPP1和可能的ENPP3的胰岛素相关作用。
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来源期刊
Amino Acids
Amino Acids 生物-生化与分子生物学
CiteScore
6.40
自引率
5.70%
发文量
99
审稿时长
2.2 months
期刊介绍: Amino Acids publishes contributions from all fields of amino acid and protein research: analysis, separation, synthesis, biosynthesis, cross linking amino acids, racemization/enantiomers, modification of amino acids as phosphorylation, methylation, acetylation, glycosylation and nonenzymatic glycosylation, new roles for amino acids in physiology and pathophysiology, biology, amino acid analogues and derivatives, polyamines, radiated amino acids, peptides, stable isotopes and isotopes of amino acids. Applications in medicine, food chemistry, nutrition, gastroenterology, nephrology, neurochemistry, pharmacology, excitatory amino acids are just some of the topics covered. Fields of interest include: Biochemistry, food chemistry, nutrition, neurology, psychiatry, pharmacology, nephrology, gastroenterology, microbiology
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