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Structural impact of pathogenic SNPs on β-tubulin using molecular dynamics study
Ummul Halilunnisa Mansoor Hussain1, Syed Ibrahim Basheer Ahamed1
1Department of Bioinformatics, School of Life Sciences, Pondicherry University, Puducherry, India.
Abstract:
Single nucleotide polymorphisms (SNPs) in the TUBB1 (β-tubulin) gene have been implicated as the primary cause of macro thrombocytopenia. Therefore it is essential to identify the potential SNPs which are harmful to cause diseases such as macro thrombocytopenia. The impact caused by these variants on β-tubulin is twofold, both structural and functional. Multiple in-silico tools were used to scrutinise the most deleterious nsSNPs (non-synonymous SNPs) via sequence and structure-based approaches. Further, the β-tubulin protein model incorporating identified mutants was subjected to MD (molecular dynamic) simulations to analyse the impact on protein structure. A total of 2974 SNPs of TUBB1 were retrieved from various sources, and 32 nsSNPs were identified. By screening through sequence-based technique, 13 variants were detected as deleterious and further structure-based filtration was carried out to find thermally destabilising variants. Finally, three variants have been detected as highly destabilising by the mCSM server and chosen for the MD study. All three variants are present in the N-terminal, Intermediate, and C-terminal regions, breaking the spatial arrangement required for microtubule assembly. The spatial arrangement of these variants is in deviation with respect to WT (wild type) β-tubulin. The protein model was subjected to a simulation period of 100 ns. The FEL analysis revealed multiple clusters with minor populations indicating the unstable conformation adapted by the β-tubulin. The normal mode vector analysis exhibited high-intensity flexible motions at the C-terminal end, responsible for binding with MAPs (microtubule-associated proteins), an essential region in microtubule assembly. All these results reveal that the SNP's predicted eventually influence the spatial arrangement of β-tubulin, which would disturb the stacking arrangement of αβ tubulin dimer in microtubule assembly. The present study may set a path to cure the diseases like macro thrombocytopenia.Communicated by Ramaswamy H. Sarma.
Insights
Single nucleotide polymorphisms (SNPs) in the TUBB1 gene cause macro thrombocytopenia. Computational analysis identified three harmful variants impacting β-tubulin structure and microtubule assembly, offering disease treatment insights.
Area of Science:
- Genetics
- Biochemistry
- Computational Biology
Background:
- Single nucleotide polymorphisms (SNPs) in the TUBB1 gene are linked to macro thrombocytopenia.
- Understanding the structural and functional impact of these variants is crucial for disease research.
Purpose of the Study:
- To identify deleterious non-synonymous SNPs (nsSNPs) in the TUBB1 gene.
- To analyze the structural and dynamic impact of identified nsSNPs on β-tubulin protein.
Main Methods:
- In-silico screening of 2974 TUBB1 SNPs to identify 32 nsSNPs.
- Sequence and structure-based analyses, including mCSM server and 100ns molecular dynamics (MD) simulations.
- Free Energy Landscape (FEL) and Normal Mode Vector (NMV) analyses were performed.
Main Results:
- Identified 13 deleterious nsSNPs, with three highly destabilizing variants selected for MD simulations.
- MD simulations revealed that these variants disrupt the spatial arrangement of β-tubulin, affecting microtubule assembly.
- FEL analysis indicated unstable protein conformations, and NMV analysis showed altered dynamics at the C-terminal MAP-binding region.
Conclusions:
- Predicted TUBB1 SNPs significantly alter β-tubulin's spatial arrangement, disrupting microtubule assembly.
- These findings provide a foundation for developing therapeutic strategies for macro thrombocytopenia.
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