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环磷酸腺苷磷酸二酯酶4(PDE4)在活细胞中的二聚化需要位于UCR1和催化单元结构域中的界面。

Dimerization of cAMP phosphodiesterase-4 (PDE4) in living cells requires interfaces located in both the UCR1 and catalytic unit domains.

作者信息

Bolger Graeme B, Dunlop Allan J, Meng Dong, Day Jon P, Klussmann Enno, Baillie George S, Adams David R, Houslay Miles D

机构信息

Departments of Medicine and Pharmacology, University of Alabama, Birmingham, AL 35294, USA.

Institute of Cardiovascular and Medical Science, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, Scotland, United Kingdom.

出版信息

Cell Signal. 2015 Apr;27(4):756-69. doi: 10.1016/j.cellsig.2014.12.009. Epub 2014 Dec 27.

Abstract

PDE4 family cAMP phosphodiesterases play a pivotal role in determining compartmentalised cAMP signalling through targeted cAMP breakdown. Expressing the widely found PDE4D5 isoform, as both bait and prey in a yeast 2-hybrid system, we demonstrated interaction consistent with the notion that long PDE4 isoforms form dimers. Four potential dimerization sites were uncovered using a scanning peptide array approach, where a recombinant purified PDE4D5 fusion protein was used to probe a 25-mer library of overlapping peptides covering the entire PDE4D5 sequence. Key residues involved in PDE4D5 dimerization were defined using a site-directed mutagenesis programme directed by an alanine scanning peptide array approach. Critical residues stabilising PDE4D5 dimerization were defined within the regulatory UCR1 region found in long, but not short, PDE4 isoforms, namely the Arg(173), Asn(174) and Asn(175) (DD1) cluster. Disruption of the DD1 cluster was not sufficient, in itself, to destabilise PDE4D5 homodimers. Instead, disruption of an additional interface, located on the PDE4 catalytic unit, was also required to convert PDE4D5 into a monomeric form. This second dimerization site on the conserved PDE4 catalytic unit is dependent upon a critical ion pair interaction. This involves Asp(463) and Arg(499) in PDE4D5, which interact in a trans fashion involving the two PDE4D5 molecules participating in the homodimer. PDE4 long isoforms adopt a dimeric state in living cells that is underpinned by two key contributory interactions, one involving the UCR modules and one involving an interface on the core catalytic domain. We propose that short forms do not adopt a dimeric configuration because, in the absence of the UCR1 module, residual engagement of the remaining core catalytic domain interface provides insufficient free energy to drive dimerization. The functioning of PDE4 long and short forms is thus poised to be inherently distinct due to this difference in quaternary structure.

摘要

磷酸二酯酶4(PDE4)家族的环磷酸腺苷(cAMP)磷酸二酯酶通过靶向性cAMP分解在决定区域化cAMP信号传导中起关键作用。在酵母双杂交系统中,我们将广泛存在的PDE4D5亚型同时作为诱饵和猎物进行表达,证实了其相互作用,这与长链PDE4亚型形成二聚体的观点一致。我们采用扫描肽阵列方法发现了四个潜在的二聚化位点,其中使用重组纯化的PDE4D5融合蛋白来探测覆盖整个PDE4D5序列的25聚体重叠肽文库。通过由丙氨酸扫描肽阵列方法指导的定点诱变程序确定了参与PDE4D5二聚化的关键残基。在长链而非短链PDE4亚型中发现的调节性UCR1区域内确定了稳定PDE4D5二聚化的关键残基,即精氨酸(173)、天冬酰胺(174)和天冬酰胺(175)(DD1)簇。DD1簇的破坏本身并不足以使PDE4D5同型二聚体不稳定。相反,还需要破坏位于PDE4催化单元上的另一个界面,才能将PDE4D5转化为单体形式。保守的PDE4催化单元上的第二个二聚化位点依赖于关键的离子对相互作用。这涉及PDE4D5中的天冬氨酸(463)和精氨酸(499),它们以反式相互作用,涉及参与同型二聚体的两个PDE4D5分子。PDE4长链亚型在活细胞中呈二聚体状态,这由两个关键的促成相互作用所支撑,一个涉及UCR模块,另一个涉及核心催化结构域上的一个界面。我们认为短链形式不采用二聚体构型,因为在没有UCR1模块的情况下,剩余核心催化结构域界面的残余结合提供的自由能不足以驱动二聚化。由于这种四级结构的差异,PDE4长链和短链形式的功能因此必然不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c233/4371794/08e7c350c7be/gr1.jpg

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