Cheng Y K, Pettitt B M
Chemistry Department, University of Houston, TX 77204-5641.
Prog Biophys Mol Biol. 1992;58(3):225-57. doi: 10.1016/0079-6107(92)90007-s.
In this selected literature survey, we have seen that the stabilities of duplexes and triplexes are governed by the vertical base stacking, the horizontal specific base-paired H-bonding and the environmental parameters. The entropic contribution in the solvation/desolvation process is important in driving the aggregation of NA strands and duplex formation, but base stacking and specific H-bonding maintain the helical order. Triplex formation shares most of the physical environmental prerequisites with those of duplex NAs. However, some additional environmental conditions are often needed. Only in low pH solution is the polycytidylic strand protonated and, thus, it is possible for the strand to bind to a G.C duplex sequence to give the C+(G.C) triplex. High ionic strength is often necessary for the screening of inter-phosphate repulsion due to the high linear charge density in triplexes. The presence of specific counterions is important for complexation. In the absence of negative supercoiling, existence of an intramolecular triplex is rare except under very acidic conditions for the formation of C+(G.C)-type intramolecular triplex. As expected, the stabilities of both inter- and intramolecular triplexes increase with sequence length. The thermodynamic principles of helix-coil transition of oligo-duplex may be described by the van't Hoff relationship, which assumes a two-state cooperative melting profile. Thus, the enthalpy, entropy and free energy of transition can be evaluated from the experimental melting curves (e.g. OD, DSC). For polynucleotides, because of the non-two-state nature of transition, the simple van't Hoff relationship is no longer valid, and direct calorimetry is needed to obtain reliable thermodynamic parameters. The pH and salt concentration dependence of duplex stability can be formulated and derived from a van't Hoff equation. Base-stacking patterns are simple in duplexes but not so in triplexes due to the diversity in triplet schemes. The sequence dependence of base stacking for duplexes has been characterized and employed to predict the stability of an arbitrary sequence. In conclusion, the stability of duplex is relatively well-characterized by thermodynamic data in terms of both base stacking and specific H-bonding. Thermodynamic studies of triplexes have been far fewer in number. Oligonucleotides have found application in the detection and localization of a mRNA or its gene, the detection of bacterial or viral sequences, and the inhibition of the translation of mRNA and the transcription and replication of DNA (Englisch and Gauss, 1991). In a different approach, oligonucleotides have been targeted directly to a DNA duplex motif of a gene in order to inhibit the expression at the beginning of the transcriptional process.(ABSTRACT TRUNCATED AT 400 WORDS)
在本次文献综述中,我们发现双链和三链的稳定性受垂直碱基堆积、水平特异性碱基配对氢键以及环境参数的影响。溶剂化/去溶剂化过程中的熵贡献对于驱动核酸链聚集和双链形成很重要,但碱基堆积和特异性氢键维持了螺旋结构。三链形成与双链核酸有许多共同的物理环境前提条件。然而,通常还需要一些额外的环境条件。只有在低pH溶液中,聚胞苷链才会质子化,因此该链有可能与G.C双链序列结合形成C+(G.C)三链。由于三链中线性电荷密度高,通常需要高离子强度来屏蔽磷酸间的斥力。特定抗衡离子的存在对于形成复合物很重要。在没有负超螺旋的情况下,分子内三链很少存在,除非在非常酸性的条件下形成C+(G.C)型分子内三链。不出所料,分子间和分子内三链的稳定性都随序列长度增加。寡聚双链螺旋-线圈转变的热力学原理可用范特霍夫关系来描述,该关系假设为两态协同解链曲线。因此,转变的焓、熵和自由能可从实验解链曲线(如OD、DSC)中评估。对于多核苷酸,由于转变的非两态性质,简单的范特霍夫关系不再有效,需要直接量热法来获得可靠的热力学参数。双链稳定性对pH和盐浓度的依赖性可以从范特霍夫方程推导得出。双链中的碱基堆积模式很简单,但由于三联体方案的多样性,三链中的碱基堆积模式并非如此。双链碱基堆积的序列依赖性已得到表征,并用于预测任意序列的稳定性。总之,就碱基堆积和特异性氢键而言,双链的稳定性通过热力学数据得到了较好的表征。对三链的热力学研究数量要少得多。寡核苷酸已应用于mRNA或其基因的检测和定位、细菌或病毒序列的检测以及mRNA翻译以及DNA转录和复制的抑制(Englisch和Gauss,1991)。另一种方法是,寡核苷酸直接靶向基因的DNA双链基序,以在转录过程开始时抑制表达。(摘要截取自400字)