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同型半胱氨酸硫内酯解毒酶与阿尔茨海默病。

Homocysteine Thiolactone Detoxifying Enzymes and Alzheimer's Disease.

机构信息

Department of Biochemistry and Biotechnology, University of Life Sciences, 60-637 Poznań, Poland.

Department of Microbiology, Biochemistry and Molecular Genetics, New Jersey Medical School, Rutgers University, International Center for Public Health, Newark, NJ 07103, USA.

出版信息

Int J Mol Sci. 2024 Jul 25;25(15):8095. doi: 10.3390/ijms25158095.

Abstract

Elevated levels of homocysteine (Hcy) and related metabolites are associated with Alzheimer's disease (AD). Severe hyperhomocysteinemia causes neurological deficits and worsens behavioral and biochemical traits associated with AD. Although Hcy is precluded from entering the Genetic Code by proofreading mechanisms of aminoacyl-tRNA synthetases, and thus is a non-protein amino acid, it can be attached to proteins via an -homocysteinylation reaction mediated by Hcy-thiolactone. Because -homocysteinylation is detrimental to a protein's function and biological integrity, Hcy-thiolactone-detoxifying enzymes-PON1, BLMH, BPHL-have evolved. This narrative review provides an account of the biological function of these enzymes and of the consequences of their impairments, leading to the phenotype characteristic of AD. Overall, accumulating evidence discussed in this review supports a hypothesis that Hcy-thiolactone contributes to neurodegeneration associated with a dysregulated Hcy metabolism.

摘要

同型半胱氨酸(Hcy)和相关代谢物水平升高与阿尔茨海默病(AD)有关。严重的高同型半胱氨酸血症可导致神经功能缺损,并加重与 AD 相关的行为和生化特征。尽管同型半胱氨酸被氨酰-tRNA 合成酶的校对机制排除在遗传密码之外,因此是一种非蛋白氨基酸,但它可以通过 Hcy-硫内酯介导的 -同型半胱氨酸化反应与蛋白质结合。由于 -同型半胱氨酸化会损害蛋白质的功能和生物完整性,因此进化出了 Hcy-硫内酯解毒酶-PON1、BLMH、BPHL。本综述叙述了这些酶的生物学功能及其功能障碍的后果,导致 AD 的表型特征。总的来说,本综述中讨论的累积证据支持了同型半胱氨酸硫内酯与 Hcy 代谢失调相关的神经退行性变有关的假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eba6/11312131/2b7b859c3081/ijms-25-08095-g001.jpg

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