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DNA发夹中内环的大小会影响它们与部分互补链的靶向作用。

The size of the internal loop in DNA hairpins influences their targeting with partially complementary strands.

作者信息

Prislan Iztok, Lee Hui-Ting, Lee Cynthia, Marky Luis A

机构信息

Department of Pharmaceutical Sciences, University of Nebraska Medical Center , 986025 Nebraska Medical Center, Omaha, Nebraska 68198-6025, United States.

出版信息

J Phys Chem B. 2015 Jan 8;119(1):96-104. doi: 10.1021/jp510131c. Epub 2014 Dec 19.

Abstract

Targeting of noncanonical DNA structures, such as hairpin loops, may have significant diagnostic and therapeutic potential. Oligonucleotides can be used for binding to mRNA, forming a DNA/RNA hybrid duplex that inhibits translation. This kind of modulation of gene expression is called the antisense approach. In order to determine the best strategy to target a common structural motif in mRNA, we have designed a set of stem-loop DNA molecules with sequence: d(GCGCTnGTAAT5GTTACTnGCGC), where n = 1, 3, or 5, "T5" is an end loop of five thymines. We used a combination of calorimetric and spectroscopy techniques to determine the thermodynamics for the reaction of a set of hairpins containing internal loops with their respective partially complementary strands. Our aim was to determine if internal- and end-loops are promising regions for targeting with their corresponding complementary strands. Indeed, all targeting reactions were accompanied by negative changes in free energy, indicating that reactions proceed spontaneously. Further investigation showed that these negative free energy terms result from a net balance of unfavorable entropy and favorable enthalpy contributions. In particular, unfolding of hairpins and duplexes is accompanied by positive changes in heat capacity, which may be a result of exposure of hydrophobic groups to the solvent. This study provides a new method for the targeting of mRNA in order to control gene expression.

摘要

靶向非经典DNA结构,如发夹环,可能具有显著的诊断和治疗潜力。寡核苷酸可用于与mRNA结合,形成抑制翻译的DNA/RNA杂交双链体。这种基因表达的调控方式称为反义方法。为了确定靶向mRNA中常见结构基序的最佳策略,我们设计了一组茎环DNA分子,其序列为:d(GCGCTnGTAAT5GTTACTnGCGC),其中n = 1、3或5,“T5”是由五个胸腺嘧啶组成的末端环。我们使用量热法和光谱技术相结合的方法,来确定一组含有内部环的发夹与其各自部分互补链反应的热力学。我们的目的是确定内部环和末端环是否是与其相应互补链靶向结合的有前景的区域。事实上,所有的靶向反应都伴随着自由能的负变化,表明反应是自发进行的。进一步的研究表明,这些负自由能项是由不利的熵和有利的焓贡献的净平衡导致的。特别是,发夹和双链体的解折叠伴随着热容的正变化,这可能是疏水基团暴露于溶剂的结果。这项研究为靶向mRNA以控制基因表达提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ba/4291056/6e5ae069a4a1/jp-2014-10131c_0004.jpg

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