Department of Biochemistry, Emory University School of Medicine, 1510 Clifton Road, Atlanta, GA, 30322, USA.
Huffington Center on Aging and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
Sci Rep. 2019 Jul 10;9(1):9966. doi: 10.1038/s41598-019-46230-8.
The lysosome plays a crucial role in the regulation of longevity. Lysosomal degradation is tightly coupled with autophagy that is induced by many longevity paradigms and required for lifespan extension. The lysosome also serves as a hub for signal transduction and regulates longevity via affecting nuclear transcription. One lysosome-to-nucleus retrograde signaling pathway is mediated by a lysosome-associated fatty acid binding protein LBP-8 in Caenorhabditis elegans. LBP-8 shuttles lysosomal lipids into the nucleus to activate lipid regulated nuclear receptors NHR-49 and NHR-80 and consequently promote longevity. However, the structural basis of LBP-8 action remains unclear. Here, we determined the first 1.3 Å high-resolution structure of this life-extending protein LBP-8, which allowed us to identify a structurally conserved nuclear localization signal and amino acids involved in lipid binding. Additionally, we described the range of fatty acids LBP-8 is capable of binding and show that it binds to life-extending ligands in worms such as oleic acid and oleoylethanolamide with high affinity.
溶酶体在寿命调控中起着至关重要的作用。溶酶体降解与自噬紧密偶联,自噬由许多长寿模型诱导,并延长寿命所必需的。溶酶体还作为信号转导的枢纽,通过影响核转录来调节寿命。溶酶体到核的逆向信号通路是由秀丽隐杆线虫中的溶酶体相关脂肪酸结合蛋白 LBP-8 介导的。LBP-8 将溶酶体脂质转运到核内,激活脂质调节的核受体 NHR-49 和 NHR-80,从而促进长寿。然而,LBP-8 作用的结构基础仍不清楚。在这里,我们确定了这种延长寿命蛋白 LBP-8 的第一个 1.3 Å 高分辨率结构,这使我们能够识别出一个结构保守的核定位信号和参与脂质结合的氨基酸。此外,我们描述了 LBP-8 能够结合的脂肪酸范围,并表明它以高亲和力结合线虫中的延长寿命配体,如油酸和油酰乙醇胺。