Zhang Wenbing, Chen Shi-Jie
Department of Physics and Astronomy and Department of Biochemistry, University of Missouri, Columbia, Missouri, USA.
Biophys J. 2006 Feb 1;90(3):778-87. doi: 10.1529/biophysj.105.062950. Epub 2005 Nov 4.
The complexity of RNA hairpin folding arises from the interplay between the loop formation, the disruption of the slow-breaking misfolded states, and the formation of the slow-forming native base stacks. We investigate the general physical mechanism for the dependence of the RNA hairpin folding kinetics on the sequence and the length of the hairpin loop and the helix stem. For example, 1), the folding would slow down when a stable GC basepair moves to the middle of the stem; 2), hairpin with GC basepair near the loop would fold/unfold faster than the one with GC near the tail of the stem; 3), within a certain range of the stem length, a longer stem can cause faster folding; and 4), certain misfolded states can assist folding through the formation of scaffold structures to lower the entropic barrier for the folding. All our findings are directly applicable and quantitatively testable in experiments. In addition, our results can be useful for molecular design to achieve desirable fast/slow-folding hairpins, hairpins with/without specific misfolded intermediates, and hairpins that fold along designed pathways.
RNA发夹折叠的复杂性源于环形成、缓慢破坏的错误折叠状态的瓦解以及缓慢形成的天然碱基堆积之间的相互作用。我们研究了RNA发夹折叠动力学对发夹环和螺旋茎的序列及长度依赖性的一般物理机制。例如,1)当一个稳定的GC碱基对移至茎的中部时,折叠会减慢;2)环附近有GC碱基对的发夹比茎尾部附近有GC碱基对的发夹折叠/解折叠更快;3)在茎长度的一定范围内,较长的茎可导致更快的折叠;4)某些错误折叠状态可通过形成支架结构来辅助折叠,以降低折叠的熵垒。我们所有的发现都可直接应用于实验且能进行定量测试。此外,我们的结果对于实现所需的快速/缓慢折叠发夹、有/无特定错误折叠中间体的发夹以及沿设计途径折叠的发夹的分子设计可能是有用的。