Janus-like behavior of intrinsically disordered regions in reticulophagy.

Autophagy Pub Date : 2025-03-01 Epub Date: 2025-01-03 DOI:10.1080/15548627.2024.2437652
Sergio Alejandro Poveda-Cuevas, Kateryna Lohachova, Borna Markusic, Ivan Dikic, Gerhard Hummer, Ramachandra M Bhaskara
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Abstract

Intrinsically disordered regions (IDRs) are crucial to homeostatic and organellar remodeling pathways. In reticulophagy/ER-phagy, long cytosolic IDR-containing receptors (e.g. RETREG1/FAM134B) house the LC3-interacting region (LIR) motif to recruit the phagophore. The precise functions of the IDR beyond engaging the autophagic machinery are unclear. Here, we comment on the role of the RETREG1-IDR based on our recent computer modeling and molecular dynamics (MD) simulations. Extensive analysis of the RETREG1-IDR indicates a continuum of conformations between expanded and compact structures, displaying a Janus-like feature. Using an adapted MARTINI model, we find that the IDR ensemble properties vary widely depending on the membrane anchor. IDRs alone are sufficient to promote and sense membrane curvature and can act as entropic tethers. When anchored to the Reticulon homology domain (RHD), they adopt compact collapsed conformations, acting as effector scaffolds that amplify RHD membrane remodeling properties, enhancing receptor-clustering and accelerating spontaneous budding. These findings expand the operational scope of IDRs within reticulophagy, offering fresh insights into a mechanistic understanding of membrane remodeling.

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网状吞噬中内在无序区域的双面样行为。
内在紊乱区(IDRs)是稳态和细胞器重塑途径的关键。在网状吞噬/ er吞噬中,长胞质含idr受体(如RETREG1/FAM134B)容纳lc3相互作用区(LIR)基序以招募吞噬细胞。除了参与自噬机制外,IDR的确切功能尚不清楚。在这里,我们基于我们最近的计算机建模和分子动力学(MD)模拟来评论RETREG1-IDR的作用。对RETREG1-IDR的广泛分析表明,在扩展结构和紧凑结构之间存在连续的构象,显示出类似两面星的特征。利用一个自适应的MARTINI模型,我们发现IDR系综性质随着膜锚的不同而变化很大。仅idr就足以促进和感知膜曲率,并可作为熵系绳。当锚定在RHD上时,它们采用紧凑的折叠构象,作为效应支架,增强RHD膜重塑特性,增强受体聚集并加速自发出芽。这些发现扩大了idr在网状吞噬中的作用范围,为膜重塑的机制理解提供了新的见解。
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