Structure of human phospholipase D3, a single-strand exonuclease associated with Alzheimer's disease

IF 4.2 The FEBS journal Pub Date : 2024-11-08 DOI:10.1111/febs.17319
Aleksandar Bijelic, Peter Macheroux
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Abstract

Phospholipase D3 (PLD3) has emerged as an important 5′-exonuclease in charge of removing single-stranded DNA in lysosomes. Rare genetic variants of the gene encoding PLD3 have been implicated in late-onset Alzheimer's disease (AD). Ishii et al. have produced the soluble domain of human PLD3 with the aim of determining its three-dimensional structure using X-ray crystallography. The high-resolution structure (2.3 Å) provides new insights into the biochemical properties of the enzyme and paves the way to a deeper understanding of amino acid replacements affecting the stability and activity of the enzyme.

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与阿尔茨海默病有关的单链外切酶--人类磷脂酶 D3 的结构。
磷脂酶D3(PLD3)已成为一种重要的5'-外切酶,负责清除溶酶体中的单链DNA。编码 PLD3 基因的罕见遗传变异与晚发性阿尔茨海默病(AD)有关。Ishii 等人制作了人类 PLD3 的可溶性结构域,目的是利用 X 射线晶体学确定其三维结构。该高分辨率结构(2.3 Å)为了解该酶的生化特性提供了新的视角,并为深入理解影响该酶稳定性和活性的氨基酸替换铺平了道路。
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