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生成和表征 DNA-GCN4 寡核苷酸-肽缀合物:DNA/蛋白质相互作用对 DNA 敏化的影响。

Generation and Characterization of a DNA-GCN4 Oligonucleotide-Peptide Conjugate: The Impact DNA/Protein Interactions on the Sensitization of DNA.

机构信息

Faculty of Chemistry, University of Gdańsk, Wita Stwosza 63, 80-308 Gdańsk, Poland.

Faculty of Chemistry, Gdańsk University of Technology, Narutowicza 11/12, 80-233 Gdańsk, Poland.

出版信息

Molecules. 2020 Aug 10;25(16):3630. doi: 10.3390/molecules25163630.

Abstract

Radiotherapy, the most common therapy for the treatment of solid tumors, exerts its effects by inducing DNA damage. To fully understand the extent and nature of this damage, DNA models that mimic the in vivo situation should be utilized. In a cellular context, genomic DNA constantly interacts with proteins and these interactions could influence both the primary radical processes (triggered by ionizing radiation) and secondary reactions, ultimately leading to DNA damage. However, this is seldom addressed in the literature. In this work, we propose a general approach to tackle these shortcomings. We synthesized a protein-DNA complex that more closely represents DNA in the physiological environment than oligonucleotides solution itself, while being sufficiently simple to permit further chemical analyses. Using click chemistry, we obtained an oligonucleotide-peptide conjugate, which, if annealed with the complementary oligonucleotide strand, forms a complex that mimics the specific interactions between the GCN4 protein and DNA. The covalent bond connecting the oligonucleotide and peptide constitutes a part of substituted triazole, which forms due to the click reaction between the short peptide corresponding to the specific amino acid sequence of GCN4 protein (yeast transcription factor) and a DNA fragment that is recognized by the protein. DNAse footprinting demonstrated that the part of the DNA fragment that specifically interacts with the peptide in the complex is protected from DNAse activity. Moreover, the thermodynamic characteristics obtained using differential scanning calorimetry (DSC) are consistent with the interaction energies calculated at the level of metadynamics. Thus, we present an efficient approach to generate a well-defined DNA-peptide conjugate that mimics a real DNA-peptide complex. These complexes can be used to investigate DNA damage under conditions very similar to those present in the cell.

摘要

放射疗法是治疗实体瘤最常用的疗法,它通过诱导 DNA 损伤来发挥作用。为了充分了解这种损伤的程度和性质,应该使用模拟体内情况的 DNA 模型。在细胞环境中,基因组 DNA 不断与蛋白质相互作用,这些相互作用可能会影响初级自由基过程(由电离辐射引发)和次级反应,最终导致 DNA 损伤。然而,这在文献中很少被提及。在这项工作中,我们提出了一种解决这些缺点的一般方法。我们合成了一种蛋白质-DNA 复合物,它比寡核苷酸溶液本身更能代表生理环境中的 DNA,同时又足够简单,可以进行进一步的化学分析。使用点击化学,我们获得了一个寡核苷酸-肽缀合物,如果与互补的寡核苷酸链退火,就会形成一个模拟 GCN4 蛋白与 DNA 之间特定相互作用的复合物。连接寡核苷酸和肽的共价键构成了取代三唑的一部分,该三唑是由于 GCN4 蛋白(酵母转录因子)的特定氨基酸序列的短肽与被该蛋白质识别的 DNA 片段之间的点击反应而形成的。DNAse 足迹实验表明,在复合物中与肽特异性相互作用的 DNA 片段部分免受 DNAse 活性的影响。此外,使用差示扫描量热法(DSC)获得的热力学特性与在元动力学水平上计算的相互作用能一致。因此,我们提出了一种有效的方法来生成一种定义明确的 DNA-肽缀合物,该缀合物模拟真实的 DNA-肽复合物。这些复合物可用于在非常类似于细胞内存在的条件下研究 DNA 损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed0/7466028/65cbcf0c1971/molecules-25-03630-g001.jpg

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