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无序肽寻找其天然环境:CB1内源性大麻素受体与肽聚糖结合的结构基础

Disordered Peptides Looking for Their Native Environment: Structural Basis of CB1 Endocannabinoid Receptor Binding to Pepcans.

作者信息

Emendato Alessandro, Guerrini Remo, Marzola Erika, Wienk Hans, Boelens Rolf, Leone Serena, Picone Delia

机构信息

Department of Chemical Sciences, University of Naples Federico II, Naples, Italy.

Department of Chemical and Pharmaceutical Sciences, University of Ferrara, Ferrara, Italy.

出版信息

Front Mol Biosci. 2018 Nov 16;5:100. doi: 10.3389/fmolb.2018.00100. eCollection 2018.

Abstract

Endocannabinoid peptides, or "pepcans," are endogenous ligands of the CB1 cannabinoid receptor. Depending on their length, they display diverse activity: For instance, the nona-peptide Pepcan-9, also known as hemopressin, is a powerful inhibitor of CB1, whereas the longer variant Pepcan-12, which extends by only three amino acid residues at the N-terminus, acts on both CB1 and CB2 as an allosteric modulator, although with diverse effects. Despite active research on their pharmacological applications, very little is known about structure-activity relationships of pepcans. Different structures have been proposed for the nona-peptide, which has also been reported to form fibrillar aggregates. This might have affected the outcome and reproducibility of bioactivity studies. In an attempt of elucidating the determinants of both biological activity and aggregation propensity of Pepcan-9 and Pepcan-12, we have performed their structure characterization in solvent systems characterized by different polarity and pH. We have found that, while disordered in aqueous environment, both peptides display helical structure in less polar environment, mimicking the proteic receptor milieu. In the case of Pepcan-9, this structure is fully consistent with the observed modulation of the CB1. For Pepcan-12, whose allosteric binding site is still unknown, the presented structure is compatible with the binding at one of the previously proposed allosteric sites on CB1. These findings open the way to structure-driven design of selective peptide modulators of CB1.

摘要

内源性大麻素肽,即“pepcans”,是CB1大麻素受体的内源性配体。根据其长度,它们表现出不同的活性:例如,九肽Pepcan-9,也称为血加压素,是CB1的强效抑制剂,而较长的变体Pepcan-12,其在N端仅延伸三个氨基酸残基,作为变构调节剂作用于CB1和CB2,尽管具有不同的作用效果。尽管对其药理学应用进行了积极研究,但关于pepcans的构效关系却知之甚少。对于九肽已经提出了不同的结构,据报道它还会形成纤维状聚集体。这可能影响了生物活性研究的结果和可重复性。为了阐明Pepcan-9和Pepcan-12的生物活性和聚集倾向的决定因素,我们在具有不同极性和pH值的溶剂系统中对它们进行了结构表征。我们发现,虽然这两种肽在水性环境中无序,但在极性较小的环境中都呈现螺旋结构,模拟了蛋白质受体环境。就Pepcan-9而言,这种结构与观察到的对CB1的调节完全一致。对于变构结合位点仍未知的Pepcan-12,所呈现的结构与先前提出的CB1上的一个变构位点的结合是相容的。这些发现为CB1选择性肽调节剂的结构驱动设计开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7a1/6250848/1bec4bd4bb43/fmolb-05-00100-g0001.jpg

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