Ensemble Allosteric Model for the Modified Wobble Hypothesis
Source abstract
Abstract
The residue 2-thiouridine (s 2 U) provides a remarkable example for the “modified wobble” hypothesis, which postulates that some post-transcriptional modifications at the wobble position of tRNAs restrict recognition of degenerate codons. Through extensive molecular dynamics simulations using our χ IDRP force field parameters, we demonstrate how this modification shifts the conformational ensemble from a predominantly disordered, as in the case of an RNA pentamer (GUUUC), to a substantially ordered population in Gs 2 UUUC. Our simulations clearly showed that the van der Waals interaction of sulfur played a major role in driving the disorder-to-order transition. The conformational redistribution and the slowing down of the transition between the clusters within the population in the presence of s 2 U suggest ensemble allostery to be a key mechanism that may play a general role in the functioning of the wobble modifications of tRNAs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: RNA modifications and cancer · RNA and protein synthesis mechanisms · RNA Research and Splicing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Biophysics, Molecular Biology and Bioinformatics, University of Calcutta, 92, Acharya Prafulla Chandra Road, Kolkata 700 009, India
Institute of Bioorganic Chemistry, Polish Academy of Sciences, Z. Noskowskiego 12/14, 61-704 Poznan, Poland
Funding
Council of Scientific and Industrial Research · University Grants Commission · Science and Engineering Research Board · Department of Science and Technology, Ministry of Science and Technology
References (35)
Show source-provided references
1. 10.1016/0300-9084(91)90163-U10.1016/0300-9084(91)90163-U ↗
2. 10.1016/S0022-2836(66)80022-010.1016/S0022-2836(66)80022-0 ↗
3. Yokoyama S. · 1995 · 207
4. 10.1073/pnas.82.15.490510.1073/pnas.82.15.4905 ↗
5. 10.1021/ja00033a04410.1021/ja00033a044 ↗
6. 10.1021/ja00257a04410.1021/ja00257a044 ↗
7. 10.1021/ja00047a00510.1021/ja00047a005 ↗
8. 10.1093/nar/25.6.127210.1093/nar/25.6.1272 ↗
9. 10.1017/S135583820000091110.1017/S1355838200000911 ↗
10. 10.1016/0014-5793(83)81123-510.1016/0014-5793(83)81123-5 ↗
11. 10.1080/15476286.2017.135656210.1080/15476286.2017.1356562 ↗
12. 10.1063/1.44586910.1063/1.445869 ↗
13. Case D. A. · 2016
14. 10.1002/1096-987X(200009)21:12<1049::AID-JCC3>3.0.CO;2-F10.1002/1096-987X(200009)21:12<1049::AID-JCC3>3.0.CO;2-F ↗
15. 10.1529/biophysj.106.09778210.1529/biophysj.106.097782 ↗
16. 10.1021/ct200162x10.1021/ct200162x ↗
17. 10.1002/jcc.2437410.1002/jcc.24374 ↗
18. 10.1021/ct600329w10.1021/ct600329w ↗
19. 10.1021/ci400582a10.1021/ci400582a ↗
20. 10.1021/jp809762b10.1021/jp809762b ↗
21. 10.1021/ct500120v10.1021/ct500120v ↗
22. 10.1103/PhysRevLett.98.15810310.1103/PhysRevLett.98.158103 ↗
23. 10.1093/nar/gkv76110.1093/nar/gkv761 ↗
24. 10.1016/0022-2836(74)90361-110.1016/0022-2836(74)90361-1 ↗
25. 10.1021/ma50003a01910.1021/ma50003a019 ↗
26. 10.1006/jmbi.1998.223310.1006/jmbi.1998.2233 ↗
27. 10.1038/nature1300110.1038/nature13001 ↗
28. 10.1021/ja200955410.1021/ja2009554 ↗
29. 10.1016/j.sbi.2019.03.00910.1016/j.sbi.2019.03.009 ↗
30. 10.1021/jacs.7b0072710.1021/jacs.7b00727 ↗
31. Liljas A. · 200910.1142/6620 ↗
32. 10.1021/bi00661a03410.1021/bi00661a034 ↗
33. 10.1021/bi00628a03510.1021/bi00628a035 ↗
34. 10.1016/0079-6107(70)90027-110.1016/0079-6107(70)90027-1 ↗
35. 10.1021/bi00644a00110.1021/bi00644a001 ↗