Reply to: Does the KDEL receptor cycle between the Golgi and the ER?
作者信息
Denecke Jurgen
机构信息
Centre for Plant Sciences, School of Biology, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, UK.
出版信息
Nat Commun. 2024 Mar 20;15(1):2454. doi: 10.1038/s41467-024-45850-7.
Abstract
摘要
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Reply to: Does the KDEL receptor cycle between the Golgi and the ER?回复：KDEL 受体是否在高尔基体和内质网之间循环？
Nat Commun. 2024 Mar 20;15(1):2454. doi: 10.1038/s41467-024-45850-7.
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Does the KDEL receptor cycle between the Golgi and the ER?KDEL 受体是否在高尔基体和内质网之间循环？
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Computational Modeling of C-Terminal Tails to Predict the Calcium-Dependent Secretion of Endoplasmic Reticulum Resident Proteins.用于预测内质网驻留蛋白钙依赖性分泌的C末端尾巴的计算模型
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A signal capture and proofreading mechanism for the KDEL-receptor explains selectivity and dynamic range in ER retrieval.KDEL 受体的信号捕获和校对机制解释了内质网回收中的选择性和动态范围。
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A Model for ERD2 Function in Higher Plants.高等植物中ERD2功能的一种模型。
Front Plant Sci. 2020 Mar 25;11:343. doi: 10.3389/fpls.2020.00343. eCollection 2020.
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A signal motif retains Arabidopsis ER-α-mannosidase I in the cis-Golgi and prevents enhanced glycoprotein ERAD.一个信号基序将拟南芥内质网-α-甘露糖苷酶 I 保留在顺面高尔基体内，并防止糖蛋白 ERAD 增强。
Nat Commun. 2019 Aug 16;10(1):3701. doi: 10.1038/s41467-019-11686-9.
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Structural basis for pH-dependent retrieval of ER proteins from the Golgi by the KDEL receptor.KDEL 受体介导内质网蛋白从高尔基体 pH 依赖性回收的结构基础。
Science. 2019 Mar 8;363(6431):1103-1107. doi: 10.1126/science.aaw2859.
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KDEL Receptors Are Differentially Regulated to Maintain the ER Proteome under Calcium Deficiency.KDEL 受体在钙离子缺乏时被差异化调控以维持内质网蛋白质组。
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Predominant Golgi Residency of the Plant K/HDEL Receptor Is Essential for Its Function in Mediating ER Retention.植物 K/HDEL 受体的主要高尔基体驻留对于其在介导内质网保留中的功能是必不可少的。
Plant Cell. 2018 Sep;30(9):2174-2196. doi: 10.1105/tpc.18.00426. Epub 2018 Aug 2.
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Arabidopsis p24δ5 and p24δ9 facilitate Coat Protein I-dependent transport of the K/HDEL receptor ERD2 from the Golgi to the endoplasmic reticulum.拟南芥 p24δ5 和 p24δ9 促进 K/HDEL 受体 ERD2 在有衣小泡蛋白 I 依赖性的情况下从高尔基体到内质网的运输。
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Fluorescence resonance energy transfer analysis of protein-protein interactions in single living cells by multifocal multiphoton microscopy.利用多焦点多光子显微镜对单个活细胞中蛋白质-蛋白质相互作用进行荧光共振能量转移分析。
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