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人源 E3 蛋白 Cbl-b 的自身抑制和磷酸化激活机制:与癌症和自身免疫性疾病相关。

Autoinhibition and phosphorylation-induced activation mechanisms of human cancer and autoimmune disease-related E3 protein Cbl-b.

机构信息

Department of Structural Biology, Faculty of Advanced Life Science, and Graduate School of Life Science, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan.

出版信息

Proc Natl Acad Sci U S A. 2011 Dec 20;108(51):20579-84. doi: 10.1073/pnas.1110712108. Epub 2011 Dec 7.

DOI:10.1073/pnas.1110712108
PMID:22158902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3251137/
Abstract

Cbl-b is a RING-type E3 ubiquitin ligase that functions as a negative regulator of T-cell activation and growth factor receptor and nonreceptor-type tyrosine kinase signaling. Cbl-b dysfunction is related to autoimmune diseases and cancers in humans. However, the molecular mechanism regulating its E3 activity is largely unknown. NMR and small-angle X-ray scattering analyses revealed that the unphosphorylated N-terminal region of Cbl-b forms a compact structure by an intramolecular interaction, which masks the interaction surface of the RING domain with an E2 ubiquitin-conjugating enzyme. Phosphorylation of Y363, located in the helix-linker region between the tyrosine kinase binding and the RING domains, disrupts the interdomain interaction to expose the E2 binding surface of the RING domain. Structural analysis revealed that the phosphorylated helix-RING region forms a compact structure in solution. Moreover, the phosphate group of pY363 is located in the vicinity of the interaction surface with UbcH5B to increase affinity by reducing their electrostatic repulsion. Thus, the phosphorylation of Y363 regulates the E3 activity of Cbl-b by two mechanisms: one is to remove the masking of the RING domain from the tyrosine kinase binding domain and the other is to form a surface to enhance binding affinity to E2.

摘要

Cbl-b 是一种 RING 型 E3 泛素连接酶,作为 T 细胞激活和生长因子受体及非受体型酪氨酸激酶信号的负调控因子发挥作用。Cbl-b 功能障碍与人类的自身免疫性疾病和癌症有关。然而,调节其 E3 活性的分子机制在很大程度上尚不清楚。NMR 和小角度 X 射线散射分析表明,未磷酸化的 Cbl-b N 端区域通过分子内相互作用形成一个紧凑的结构,从而掩盖了 RING 结构域与 E2 泛素连接酶的相互作用表面。位于酪氨酸激酶结合和 RING 结构域之间的螺旋连接区的 Y363 磷酸化破坏了结构域间相互作用,从而暴露 RING 结构域的 E2 结合表面。结构分析表明,磷酸化的螺旋-RING 区域在溶液中形成一个紧凑的结构。此外,pY363 的磷酸基团位于与 UbcH5B 的相互作用表面附近,通过减少静电排斥来增加亲和力。因此,Y363 的磷酸化通过两种机制调节 Cbl-b 的 E3 活性:一种是去除 RING 结构域与酪氨酸激酶结合结构域的掩蔽作用,另一种是形成一个表面以增强与 E2 的结合亲和力。

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