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DNA纳米阵列揭示电子诱导DNA链断裂的序列依赖性

Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays.

作者信息

Keller Adrian, Rackwitz Jenny, Cauët Emilie, Liévin Jacques, Körzdörfer Thomas, Rotaru Alexandru, Gothelf Kurt V, Besenbacher Flemming, Bald Ilko

机构信息

1] Interdisciplinary Nanoscience Center (iNANO) and Danish National Research Foundation: Centre for DNA Nanotechnology (CDNA), Aarhus University, 8000 Aarhus C, Denmark [2] Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf, Dresden, Germany.

Institute of Chemistry - Physical Chemistry, University of Potsdam, Potsdam, Germany.

出版信息

Sci Rep. 2014 Dec 9;4:7391. doi: 10.1038/srep07391.

Abstract

The electronic structure of DNA is determined by its nucleotide sequence, which is for instance exploited in molecular electronics. Here we demonstrate that also the DNA strand breakage induced by low-energy electrons (18 eV) depends on the nucleotide sequence. To determine the absolute cross sections for electron induced single strand breaks in specific 13 mer oligonucleotides we used atomic force microscopy analysis of DNA origami based DNA nanoarrays. We investigated the DNA sequences 5'-TT(XYX)3TT with X = A, G, C and Y = T, BrU 5-bromouracil and found absolute strand break cross sections between 2.66 · 10(-14) cm(2) and 7.06 · 10(-14) cm(2). The highest cross section was found for 5'-TT(ATA)3TT and 5'-TT(ABrUA)3TT, respectively. BrU is a radiosensitizer, which was discussed to be used in cancer radiation therapy. The replacement of T by BrU into the investigated DNA sequences leads to a slight increase of the absolute strand break cross sections resulting in sequence-dependent enhancement factors between 1.14 and 1.66. Nevertheless, the variation of strand break cross sections due to the specific nucleotide sequence is considerably higher. Thus, the present results suggest the development of targeted radiosensitizers for cancer radiation therapy.

摘要

DNA的电子结构由其核苷酸序列决定,例如在分子电子学中就利用了这一点。在此我们证明,低能电子(18 eV)诱导的DNA链断裂也取决于核苷酸序列。为了确定特定13聚体寡核苷酸中电子诱导单链断裂的绝对截面,我们对基于DNA折纸术的DNA纳米阵列进行了原子力显微镜分析。我们研究了5'-TT(XYX)3TT序列,其中X = A、G、C,Y = T、5-溴尿嘧啶(BrU),发现绝对链断裂截面在2.66·10⁻¹⁴ cm²至7.06·10⁻¹⁴ cm²之间。分别在5'-TT(ATA)3TT和5'-TT(ABrUA)3TT中发现了最高的截面。BrU是一种放射增敏剂,被认为可用于癌症放射治疗。将BrU替代研究的DNA序列中的T会导致绝对链断裂截面略有增加,序列依赖性增强因子在1.14至1.66之间。然而,由于特定核苷酸序列导致的链断裂截面变化要大得多。因此,目前的结果表明可开发用于癌症放射治疗的靶向放射增敏剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ce0/4260214/4822c108eb5f/srep07391-f1.jpg

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