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通过计算和实验研究揭示的TLR7与秋水仙碱衍生物之间的新型相互作用

A Novel Interaction Between the TLR7 and a Colchicine Derivative Revealed Through a Computational and Experimental Study.

作者信息

Gentile Francesco, Deriu Marco A, Barakat Khaled, Danani Andrea, Tuszynski Jack

机构信息

Department of Physics, University of Alberta, AB T6G 2E1 Edmonton, Canada.

Istituto Dalle Molle di Studi Sull'intelligenza Artificiale (IDSIA), Scuola Universitaria Professionale della Svizzera Italiana (SUPSI), Università della Svizzera Italiana (USI), CH-6928 Manno, Switzerland.

出版信息

Pharmaceuticals (Basel). 2018 Feb 16;11(1):22. doi: 10.3390/ph11010022.

Abstract

The Toll-Like Receptor 7 (TLR7) is an endosomal membrane receptor involved in the innate immune system response. Its best-known small molecule activators are imidazoquinoline derivatives such as imiquimod (R-837) and resiquimod (R-848). Recently, an interaction between R-837 and the colchicine binding site of tubulin was reported. To investigate the possibility of an interaction between structural analogues of colchicine and the TLR7, a recent computational model for the dimeric form of the TLR7 receptor was used to determine a possible interaction with a colchicine derivative called CR42-24, active as a tubulin polymerization inhibitor. The estimated values of the binding energy of this molecule with respect to the TLR7 receptor were comparable to the energies of known binders as reported in a previous study. The binding to the TLR7 was further assessed by introducing genetic transformations in the TLR7 gene in cancer cell lines and exposing them to the compound. A negative shift of the IC50 value in terms of cell growth was observed in cell lines carrying the mutated TLR7 gene. The reported study suggests a possible interaction between TLR7 and a colchicine derivative, which can be explored for rational design of new drugs acting on this receptor by using a colchicine scaffold for additional modifications.

摘要

Toll样受体7(TLR7)是一种参与先天性免疫系统反应的内体膜受体。其最知名的小分子激活剂是咪唑喹啉衍生物,如咪喹莫特(R-837)和瑞喹莫特(R-848)。最近,有报道称R-837与微管蛋白的秋水仙碱结合位点之间存在相互作用。为了研究秋水仙碱结构类似物与TLR7之间相互作用的可能性,最近使用了一种TLR7受体二聚体形式的计算模型,来确定与一种名为CR42-24的秋水仙碱衍生物的可能相互作用,该衍生物作为微管蛋白聚合抑制剂具有活性。相对于TLR7受体,该分子结合能的估计值与先前研究中报道的已知结合剂的能量相当。通过在癌细胞系的TLR7基因中引入基因转化并使其暴露于该化合物,进一步评估了其与TLR7的结合。在携带突变TLR7基因的细胞系中,观察到细胞生长方面IC50值的负向变化。所报道的研究表明TLR7与秋水仙碱衍生物之间可能存在相互作用,这可以通过使用秋水仙碱支架进行额外修饰来探索用于合理设计作用于该受体的新药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a7/5874718/676edb9843e1/pharmaceuticals-11-00022-g001.jpg

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