A new entropy model for RNA: part I. A critique of the standard Jacobson-Stockmayer model applied to multiple cross links

Submitted: 30 May 2011
Accepted: 6 February 2012
Published: 24 July 2012
Abstract Views: 3302
PDF: 603
APPENDICES: 3
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The Jacobson-Stockmayer (JS) model is used in a number of standard programs for calculating the conformational entropy of RNA (and proteins). However, it is shown in this study that, in certain limiting cases, the current form of this model can lead to highly unphysical conclusions. The origin of this behavior can be traced to misunderstandings that occurred during the development of the model as applied to folded, single-stranded RNA. Here we show that an alternative model known as the cross linking entropy (CLE) model can overcome these issues. The principal object that causes entropy loss on a global scale in the CLE model is the stem, the primary measure of structural order in such coarse-grained calculations. The principal objects in the JS-model are various types of loops, and, with the exception of the hairpin loop, they are topologically local in character. To extract experimentally measurable variables, a simplified version of the CLE model is developed that resembles many features of the contact order model used in RNA and protein folding. These modifications are then applied to single molecule force-extension experiments (molecular tweezers) to extract quantitative information. It is further shown that a crude derivative of the CLE model itself can be derived directly from the JS-model when the misunderstandings are examined and corrected.

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Supporting Agencies

Japan International Science and Technology Exchange Center (JISTEC) and Ministry of Education, Culture, Sports, Science and Technology (MEXT)

How to Cite

Dawson, W., Yamamoto, K., & Kawai, G. (2012). A new entropy model for RNA: part I. A critique of the standard Jacobson-Stockmayer model applied to multiple cross links. Journal of Nucleic Acids Investigation. https://doi.org/10.4081/jnai.2650