High-resolution MD Simulation Studies to Get Mechanistic Insights into the Urea-induced Denaturation of Human Sphingosine Kinase 1

• Published in: Current topics in medicinal chemistry Vol. 21; no. 31; p. 2839
• Main Authors: Khan, Faez Iqbal, Ali, Shahid, Chen, Wenjing, Anjum, Farah, Shafie, Alaa, Hassan, Md Imtaiyaz, Lai, Dakun
• Format: Journal Article
• Language: English
• Published: United Arab Emirates 01.01.2021
• Subjects: Circular Dichroism; Humans; Molecular Dynamics Simulation; Phosphotransferases (Alcohol Group Acceptor) - chemistry; Phosphotransferases (Alcohol Group Acceptor) - metabolism; Protein Conformation; Protein Denaturation - drug effects; Protein Folding; Protein Unfolding - drug effects; Spectrometry, Fluorescence; Urea - pharmacology; MD simulation; Protein stability; Gibbs free energy; Protein denaturation; Sphingosine kinase 1; Protein folding
• ISSN: 1873-4294
• DOI: 10.2174/1568026621666211105095731

Sphingosine kinase 1 (SPhK1) is a crucial signaling enzyme involved in cell proliferation, cellular survival, stimulation of angiogenesis, and apoptosis prevention. Recently, we have reported the unfolding kinetics of SPhK1 using molecular dynamics (MD) simulation, circular dichroism, and fluorescence spectroscopy. We found that SPhK1 showed a biphasic unfolding with an intermediate state (~ 4.0 M urea). We aim to understand the impact of MD simulation duration on the structure, function, and dynamics of proteins. In order to get deeper insights into the folding mechanism, an extended MD simulation is required. Here, we extended the MD simulations time scale from 100 to 300 ns on SPhK1 at increasing urea concentration to explore structural changes in the SPhK1. The results suggested a constant form of the unfolding of SPhK1 upon extending the simulation time scale at different urea concentrations. Furthermore, we showed step by step unfolding and percentage of secondary structure contents in SPhK1 under the influence of urea at each concentration. The results from the current work revealed a uniform pattern of the SPhK1 unfolding at different urea concentrations. This study provides deeper mechanistic insights into the urea-induced denaturation of SPhK1.