From the Department of Pharmacology and Therapeutics and Cell Information Systems Group and.
Department of Biochemistry and Groupe de Recherche Axé sur la Structure des Protéines, McGill University, Montreal, Quebec H3G 0B1, Canada and.
J Biol Chem. 2018 Oct 5;293(40):15556-15568. doi: 10.1074/jbc.RA118.002640. Epub 2018 Aug 24.
In the last decade, intramembrane proteases have gained increasing attention because of their many links to various diseases. Nevertheless, our understanding as to how they function or how they are regulated is still limited, especially when it comes to human homologues. In this regard, here we sought to unravel mechanisms of regulation of the protease rhomboid-like protein-4 (RHBDL4), one of five active human serine intramembrane proteases. In view of our recent finding that human RHBDL4 efficiently cleaves the amyloid precursor protein (APP), a key protein in the pathology of Alzheimer's disease, we used established reagents to modulate the cellular cholesterol content and analyzed the effects of this modulation on RHBDL4-mediated processing of endogenous APP. We discovered that lowering membrane cholesterol levels increased the levels of RHBDL4-specific endogenous APP fragments, whereas high cholesterol levels had the opposite effect. Direct binding of cholesterol to APP did not mediate these modulating effects of cholesterol. Instead, using homology modeling, we identified two potential cholesterol-binding motifs in the transmembrane helices 3 and 6 of RHBDL4. Substitution of the essential tyrosine residues of the potential cholesterol-binding motifs to alanine increased the levels of endogenous APP C-terminal fragments, reflecting enhanced RHBDL4 activity. In summary, we provide evidence that the activity of RHBDL4 is regulated by cholesterol likely through a direct binding of cholesterol to the enzyme.
在过去的十年中,由于其与各种疾病的许多联系,跨膜蛋白酶受到了越来越多的关注。然而,我们对它们的功能或如何调节它们的理解仍然有限,特别是在涉及人类同源物时。在这方面,我们试图阐明蛋白酶类蛋白 RHBDL4 的调节机制,RHBDL4 是五种活跃的人类丝氨酸跨膜蛋白酶之一。鉴于我们最近发现人类 RHBDL4 能够有效地切割淀粉样前体蛋白(APP),APP 是阿尔茨海默病病理的关键蛋白,我们使用现有的试剂来调节细胞胆固醇含量,并分析这种调节对 RHBDL4 介导的内源性 APP 加工的影响。我们发现,降低膜胆固醇水平会增加 RHBDL4 特异性内源性 APP 片段的水平,而高胆固醇水平则会产生相反的效果。胆固醇与 APP 的直接结合并没有介导胆固醇的这种调节作用。相反,我们通过同源建模,在 RHBDL4 的跨膜螺旋 3 和 6 中鉴定出两个潜在的胆固醇结合基序。将潜在的胆固醇结合基序中的必需酪氨酸残基突变为丙氨酸会增加内源性 APP C 端片段的水平,反映出 RHBDL4 活性增强。总之,我们提供的证据表明,胆固醇可能通过直接与酶结合来调节 RHBDL4 的活性。