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基于通路表达谱分析方法估算吡咯-咪唑聚酰胺结合的全基因组脱靶效应。

Estimating genome-wide off-target effects for pyrrole-imidazole polyamide binding by a pathway-based expression profiling approach.

机构信息

Laboratory of Cancer Genetics, Chiba Cancer Center Research Institute, Chuo-ku, Chiba, Japan.

Artificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology (AIST), Koto-ku, Tokyo, Japan.

出版信息

PLoS One. 2019 Apr 9;14(4):e0215247. doi: 10.1371/journal.pone.0215247. eCollection 2019.

Abstract

In the search for new pharmaceutical leads, especially with DNA-binding molecules or genome editing methods, the issue of side and off-target effects have always been thorny in nature. A particular case is the investigation into the off-target effects of N-methylpyrrole-N-methylimidazole polyamides, a naturally inspired class of DNA binders with strong affinity to the minor-groove and sequence specificity, but at < 20 bases, their relatively short motifs also insinuate the possibility of non-unique genomic binding. Binding at non-intended loci potentially lead to the rise of off-target effects, issues that very few approaches are able to address to-date. We here report an analytical method to infer off-target binding, via expression profiling, based on probing the relative impact to various biochemical pathways; we also proposed an accompanying side effect prediction engine for the systematic screening of candidate polyamides. This method marks the first attempt in PI polyamide research to identify elements in biochemical pathways that are sensitive to the treatment of a candidate polyamide as an approach to infer possible off-target effects. Expression changes were then considered to assess possible outward phenotypic changes, manifested as side effects, should the same PI polyamide candidate be administered clinically. We validated some of these effects with a series of animal experiments, and found agreeable corroboration in certain side effects, such as changes in aspartate transaminase levels in ICR and nude mice post-administration.

摘要

在寻找新的药物先导物,特别是与 DNA 结合分子或基因组编辑方法相关时,副反应和脱靶效应一直是一个棘手的问题。一个特殊的例子是对 N-甲基吡咯-N-甲基咪唑聚酰胺的脱靶效应的研究,这类聚酰胺是一类受自然启发的 DNA 结合物,对小沟和序列特异性具有很强的亲和力,但长度小于 20 个碱基,它们相对较短的基序也暗示了非独特基因组结合的可能性。在非预期的靶标结合处潜在地导致脱靶效应的产生,这是迄今为止极少数方法能够解决的问题。在这里,我们报告了一种通过表达谱探测各种生化途径的相对影响来推断脱靶结合的分析方法;我们还提出了一个伴随的副作用预测引擎,用于对候选聚酰胺进行系统筛选。这种方法标志着 PI 聚酰胺研究中首次尝试识别生化途径中的元素,这些元素对候选聚酰胺的处理敏感,作为推断可能的脱靶效应的一种方法。然后考虑表达变化,以评估如果相同的 PI 聚酰胺候选物在临床上给药,是否可能出现外在表型变化,表现为副作用。我们通过一系列动物实验验证了其中的一些效应,并在某些副作用中发现了可接受的佐证,例如 ICR 和裸鼠给药后天冬氨酸转氨酶水平的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ec9/6456183/e5f78b01cf5b/pone.0215247.g001.jpg

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