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PKN1 相关丝氨酸/苏氨酸蛋白激酶 N1 (PKN1)内的脂质结合区域对其调节所必需的。

Lipid-Binding Regions within PKC-Related Serine/Threonine Protein Kinase N1 (PKN1) Required for Its Regulation.

机构信息

Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan.

Department of Biochemistry and Molecular Biology, University of Melbourne, Victoria 3010, Australia.

出版信息

Biochemistry. 2024 Mar 19;63(6):743-753. doi: 10.1021/acs.biochem.4c00009. Epub 2024 Mar 5.

Abstract

PKC-related serine/threonine protein kinase N1 (PKN1) is a protease/lipid-activated protein kinase that acts downstream of the RhoA and Rac1 pathways. PKN1 comprises unique regulatory, hinge region, and PKC homologous catalytic domains. The regulatory domain harbors two homologous regions, i.e., HR1 and C2-like. HR1 consists of three heptad repeats (HR1a, HR1b, and HR1c), with PKN1-(HR1a) hosting an amphipathic high-affinity cardiolipin-binding site for phospholipid interactions. Cardiolipin and C18:1 oleic acid are the most potent lipid activators of PKN1. PKN1-(C2) contains a pseudosubstrate sequence overlapping that of C20:4 arachidonic acid. However, the cardiolipin-binding site(s) within PKN1-(C2) and the respective binding properties remain unclear. Herein, we reveal (i) that the primary PKN1-(C2) sequence contains conserved amphipathic cardiolipin-binding motif(s); (ii) that trimeric PKN1-(C2) predominantly adopts a β-stranded conformation; (iii) that two distinct types of cardiolipin (or phosphatidic acid) binding occur, with the hydrophobic component playing a key role at higher salt levels; (iv) the multiplicity of C18 fatty acid binding to PKN1-(C2); and (v) the relevance of our lipid-binding parameters for PKN1-(C2) in terms of kinetic parameters previously determined for the full-length PKN1 enzyme. Thus, our discoveries create opportunities to design specific mammalian cell inhibitors that disrupt the localization of membrane-associated PKN1 signaling molecules.

摘要

蛋白激酶 C 相关丝氨酸/苏氨酸蛋白激酶 N1(PKN1)是一种位于 RhoA 和 Rac1 通路下游的蛋白酶/脂激活蛋白激酶。PKN1 由独特的调节、铰链区和蛋白激酶 C 同源催化结构域组成。调节结构域包含两个同源区域,即 HR1 和 C2 样结构域。HR1 由三个七肽重复(HR1a、HR1b 和 HR1c)组成,PKN1-(HR1a)含有一个亲脂性高亲和力心磷脂结合位点,用于与磷脂相互作用。心磷脂和 C18:1 油酸是 PKN1 最有效的脂质激活剂。PKN1-(C2)包含一个重叠 C20:4 花生四烯酸的伪底物序列。然而,PKN1-(C2)内的心磷脂结合位点及其相应的结合特性尚不清楚。在此,我们揭示了:(i)PKN1-(C2)的主要序列包含保守的两亲性心磷脂结合模体;(ii)三聚体 PKN1-(C2)主要采用β-折叠构象;(iii)发生两种不同类型的心磷脂(或磷脂酸)结合,其中疏水性成分在较高盐水平下起关键作用;(iv)多种 C18 脂肪酸与 PKN1-(C2)结合;以及(v)我们的脂质结合参数对于 PKN1-(C2)在先前确定的全长 PKN1 酶的动力学参数方面的相关性。因此,我们的发现为设计特定的哺乳动物细胞抑制剂提供了机会,这些抑制剂可以破坏膜相关 PKN1 信号分子的定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad47/10956426/daf5982db0c1/bi4c00009_0001.jpg

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