Araque J C, Robert M A
Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, USA.
Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas 77005, USA.
J Chem Phys. 2016 Mar 28;144(12):125101. doi: 10.1063/1.4943577.
Because oligonucleotides are short sequences of nucleic acid bases, their association in solution with complementary strands (hybridization) is often seen to conform to a simple two-state model. However, experimental evidence suggests that, despite their short length, oligonucleotides may hybridize through multiple states involving intermediates. We investigate whether these apparently contradictory scenarios are possible by imposing different levels of sequence specificity on a lattice model of oligonucleotides in solution, which we introduced in Part I [J. C. Araque et al., J. Chem. Phys. 134, 165103 (2011)]. We find that both multiple-intermediate (weakly cooperative) and two-state (strongly cooperative) transitions are possible and that these are directly linked to the level of sequence specificity. Sequences with low specificity hybridize (base-by-base) by way of multiple stable intermediates with increasing number of paired bases. Such intermediate states are weakly cooperative because the energetic gain from adding an additional base pair is outweighed by the conformational entropy loss. Instead, sequences with high specificity hybridize through multiple metastable intermediates which easily bridge the configurational and energetic gaps between single- and double-stranded states. These metastable intermediates interconvert with minimal loss of conformational entropy leading to a strongly cooperative hybridization. The possibility of both scenarios, multiple- and two-states, is therefore encoded in the specificity of the sequence which in turn defines the level of cooperativity.
由于寡核苷酸是核酸碱基的短序列,它们在溶液中与互补链的结合(杂交)通常被认为符合简单的两态模型。然而,实验证据表明,尽管寡核苷酸长度较短,但它们可能通过涉及中间体的多个状态进行杂交。我们通过对溶液中寡核苷酸的晶格模型施加不同程度的序列特异性来研究这些明显相互矛盾的情况是否可能,该晶格模型我们在第一部分中已经介绍过[J. C. Araque等人,《化学物理杂志》134, 165103 (2011)]。我们发现多中间体(弱协同)和两态(强协同)转变都是可能的,并且这些直接与序列特异性水平相关。特异性低的序列通过具有越来越多配对碱基的多个稳定中间体(逐个碱基地)进行杂交。这些中间状态是弱协同的,因为添加额外碱基对所获得的能量增益被构象熵损失所抵消。相反,特异性高的序列通过多个亚稳态中间体进行杂交,这些中间体很容易弥合单链和双链状态之间的构型和能量差距。这些亚稳态中间体以最小的构象熵损失相互转化,导致强协同杂交。因此,多态和两态这两种情况的可能性都编码在序列的特异性中,而序列特异性又反过来定义了协同程度。