AP3B1 facilitates PDIA3/ERP57 function to regulate rabies virus glycoprotein selective degradation and viral entry.

Autophagy Pub Date : 2024-12-01 Epub Date: 2024-08-17 DOI:10.1080/15548627.2024.2390814
Yuelan Zhang, Xinyi Zhang, Xue Yang, Linyue Lv, Qinyang Wang, Shaowei Zeng, Zhuyou Zhang, Martin Dorf, Shitao Li, Ling Zhao, Bishi Fu
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Abstract

Rabies virus causes an estimated 59,000 annual fatalities worldwide and promising therapeutic treatments are necessary to develop. In this study, affinity tag-purification mass spectrometry was employed to delineate RABV glycoprotein and host protein interactions, and PDIA3/ERP57 was identified as a potential inhibitor of RABV infection. PDIA3 restricted RABV infection with follow mechanisms: PDIA3 mediated the degradation of RABV G protein by targeting lysine 332 via the selective macroautophagy/autophagy pathway; The PDIA3 interactor, AP3B1 (adaptor related protein complex 3 subunit beta 1) was indispensable in PDIA3-triggered selective degradation of the G protein; Furthermore, PDIA3 competitively bound with NCAM1/NCAM (neural cell adhesion molecule 1) to block RABV G, hindering viral entry into host cells. PDIA3 190-199 aa residues bound to the RABV G protein were necessary and sufficient to defend against RABV. These results demonstrated the therapeutic potential of biologics that target PDIA3 or utilize PDIA3 190-199 aa peptide to treat clinical rabies.Abbreviation: aa: amino acids; ANXA2: annexin A2; AP-MS: affinity tag purification-mass spectrometry; AP3B1: adaptor related protein complex 3 subunit beta 1; ATP6V1A: ATPase H+ transporting V1 subunit A; ATP6V1H: ATPase H+ transporting V1 subunit H; BafA1: bafilomycin A1; CHX: cycloheximide; co-IP: co-immunoprecipitation; DDX17: DEAD-box helicase 17; DmERp60: drosophila melanogaster endoplasmic reticulum p60; EBOV: Zaire ebolavirus virus; EV: empty vector; GANAB: glucosidase II alpha subunit; G protein: glycoprotein; GRM2/mGluR2: glutamate metabotropic receptor 2; HsPDIA3: homo sapiens protein disulfide isomerase family A member 3; IAV: influenza virus; ILF2: interleukin enhancer binding factor 2; KO: knockout; MAGT1: magnesium transporter 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MmPDIA3: mus musculus protein disulfide isomerase associated 3; NCAM1/NCAM: neural cell adhesion molecule 1; NGFR/p75NTR: nerve growth factor receptor; NGLY1: N-glycanase 1; OTUD4: OTU deubiquitinase 4; PDI: protein disulfide isomerase; PPIs: protein-protein interactions; RABV: rabies virus; RUVBL2: RuvB like AAA ATPase 2; SCAMP3: secretory carrier membrane protein 3; ScPdi1: Saccharomyces cerevisiae s288c protein disulfide isomerase 1; SLC25A6: solute carrier family 25 member 6; SQSTM1/p62: sequestosome 1; VSV: vesicular stomatitis virus.

AP3B1 有助于 PDIA3/ERP57 发挥调节狂犬病病毒糖蛋白选择性降解和病毒进入的功能。
据估计,狂犬病病毒每年在全球造成 59,000 人死亡,因此有必要开发有前景的治疗方法。本研究采用亲和标记纯化质谱法阐明了 RABV 糖蛋白与宿主蛋白的相互作用,并确定 PDIA3/ERP57 为 RABV 感染的潜在抑制剂。PDIA3 通过以下机制限制 RABV 感染:PDIA3通过选择性大自噬/自噬途径靶向赖氨酸332,介导RABV G蛋白降解;PDIA3互作因子AP3B1(适配相关蛋白复合物3亚基β1)在PDIA3触发的G蛋白选择性降解中不可或缺;此外,PDIA3与NCAM1/NCAM(神经细胞粘附分子1)竞争性结合,阻断RABV G,阻碍病毒进入宿主细胞。与 RABV G 蛋白结合的 PDIA3 190-199 aa 残基是抵御 RABV 的必要和充分条件。这些结果表明,靶向 PDIA3 或利用 PDIA3 190-199 aa 肽的生物制剂具有治疗临床狂犬病的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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