scholarly journals Discovery of Novel GR Ligands toward Druggable GR Antagonist Conformations Identified by MD Simulations and Markov State Model Analysis

2021 ◽  
pp. 2102435
Author(s):  
Xueping Hu ◽  
Jinping Pang ◽  
Jintu Zhang ◽  
Chao Shen ◽  
Xin Chai ◽  
...  
2018 ◽  
Vol 114 (3) ◽  
pp. 274a
Author(s):  
Giulia Morra ◽  
Asghar M. Razavi ◽  
Kalpana Pandey ◽  
Harel Weinstein ◽  
Anant K. Menon ◽  
...  

2021 ◽  
Vol 17 (4) ◽  
pp. 2022-2033
Author(s):  
François Sicard ◽  
Vladimir Koskin ◽  
Alessia Annibale ◽  
Edina Rosta

Biomolecules ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 889
Author(s):  
Shuangyan Zhou ◽  
Jie Cheng ◽  
Ting Yang ◽  
Mingyue Ma ◽  
Wenying Zhang ◽  
...  

Misfolding and aggregation of transthyretin (TTR) is widely known to be responsible for a progressive systemic disorder called amyloid transthyretin (ATTR) amyloidosis. Studies suggest that TTR aggregation is initiated by a rate-limiting dissociation of the homo-tetramer into its monomers, which can rapidly misfold and self-assemble into amyloid fibril. Thus, exploring conformational change involved in TTR monomer misfolding is of vital importance for understanding the pathogenesis of ATTR amyloidosis. In this work, microsecond timescale hybrid-resolution molecular dynamics (MD) simulations combined with Markov state model (MSM) analysis were performed to investigate the misfolding mechanism of the TTR monomer. The results indicate that a macrostate with partially unfolded conformations may serve as the misfolded state of the TTR monomer. This misfolded state was extremely stable with a very large equilibrium probability of about 85.28%. With secondary structure analysis, we found the DAGH sheet in this state to be significantly destroyed. The CBEF sheet was relatively stable and sheet structure was maintained. However, the F-strand in this sheet was likely to move away from E-strand and reform a new β-sheet with the H-strand. This observation is consistent with experimental finding that F and H strands in the outer edge drive the misfolding of TTR. Finally, transition pathways from a near native state to this misfolded macrostate showed that the conformational transition can occur either through a native-like β-sheet intermediates or through partially unfolded intermediates, while the later appears to be the main pathway. As a whole, we identified a potential misfolded state of the TTR monomer and elucidated the misfolding pathway for its conformational transition. This work can provide a valuable theoretical basis for understanding of TTR aggregation and the pathogenesis of ATTR amyloidosis at the atomic level.


2020 ◽  
Vol 142 (51) ◽  
pp. 21344-21352
Author(s):  
Jingwei Weng ◽  
Maohua Yang ◽  
Wenning Wang ◽  
Xin Xu ◽  
Zhongqun Tian

2014 ◽  
Vol 10 (8) ◽  
pp. e1003767 ◽  
Author(s):  
Shuo Gu ◽  
Daniel-Adriano Silva ◽  
Luming Meng ◽  
Alexander Yue ◽  
Xuhui Huang

2020 ◽  
Vol 16 (6) ◽  
pp. 3879-3888
Author(s):  
Trayder Thomas ◽  
Elizabeth Yuriev ◽  
David K. Chalmers

2021 ◽  
Vol 120 (3) ◽  
pp. 302a-303a
Author(s):  
Joao Marcelo Lamim Ribeiro ◽  
Leslie A. Salas-Estrada ◽  
Davide Provasi ◽  
Jordana K. Thibado ◽  
Josh T. Levitz ◽  
...  

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