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P4-ATP 酶磷脂翻转酶 ATP8A2 的 N 端和 C 端片段的结构与功能特性

Structural and functional properties of the N- and C-terminal segments of the P4-ATPase phospholipid flippase ATP8A2.

作者信息

Matsell Eli, Mazaheri Moloud, Andersen Jens Peter, Molday Robert S

机构信息

Department of Biochemistry & Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada.

Department of Biomedicine, Aarhus University, Aarhus, Denmark.

出版信息

J Biol Chem. 2025 Jan;301(1):108065. doi: 10.1016/j.jbc.2024.108065. Epub 2024 Dec 9.

Abstract

ATP8A2 is a P4-ATPase that actively flips phosphatidylserine and to a lesser extent phosphatidylethanolamine across cell membranes to generate and maintain transmembrane phospholipid asymmetry. The importance of this flippase is evident in the finding that loss-of-function mutations in ATP8A2 are known to cause the neurodevelopmental disease known as cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4 (CAMRQ4) in humans and related neurodegenerative disorders in mice. Although significant progress has been made in understanding mechanisms underlying phospholipid binding and transport across the membrane domain, little is known about the structural and functional properties of the cytosolic N- and C-terminal segments of this flippase. In addition, there has been uncertainty regarding the methionine start site of ATP8A2 and accordingly the size of the N-terminal segment. Here, we have used mass spectrometry to show that bovine ATP8A2 like its human counterpart has an extended N-terminal segment not apparent in the mouse ortholog. This segment greatly enhances the expression of ATP8A2 without affecting its cellular localization or phosphatidylserine-activated ATPase activity. Using a cleavable C-terminal protein and site-directed mutagenesis, we further show that the conserved GYAFS motif in the C-terminal segment plays a role in autoinhibition as well as efficient folding of ATP8A2 into a functional protein.

摘要

ATP8A2是一种P4-ATP酶,它能主动将磷脂酰丝氨酸以及在较小程度上的磷脂酰乙醇胺翻转穿过细胞膜,以产生并维持跨膜磷脂不对称性。这种翻转酶的重要性在以下发现中得以体现:已知ATP8A2功能丧失突变会导致人类患神经发育疾病,即小脑共济失调、智力障碍和失衡综合征4(CAMRQ4),以及小鼠患相关神经退行性疾病。尽管在理解磷脂结合和跨膜结构域转运的潜在机制方面已取得显著进展,但对于这种翻转酶胞质N端和C端片段的结构和功能特性却知之甚少。此外,关于ATP8A2的甲硫氨酸起始位点以及相应的N端片段大小一直存在不确定性。在这里,我们利用质谱表明,牛ATP8A2与其人类对应物一样,具有在小鼠直系同源物中不明显的延长N端片段。该片段极大地增强了ATP8A2的表达,而不影响其细胞定位或磷脂酰丝氨酸激活的ATP酶活性。通过使用可切割的C端蛋白和定点诱变,我们进一步表明,C端片段中保守的GYAFS基序在自抑制以及ATP8A2有效折叠成功能蛋白方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a1f/11750469/406845dbbac1/gr1.jpg

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