A Comprehensive Study on the Electrostatic Properties of Tubulin-Tubulin Complexes in Microtubules

• Published in: Cells (Basel, Switzerland) Switzerland), 2023-01, Vol.12 (2), p.238
• Main Authors: Guo, Wenhan, Ale, Tolulope Ayodeji, Sun, Shengjie, Sanchez, Jason E, Li, Lin
• Format: Article
• Language: English
• Subjects: Cell cycle; DelPhi; DelPhiForce; Electric fields; Electrostatic properties; Hydrogen bonds; Interfaces; microtubule; Microtubules; Microtubules - metabolism; molecular dynamics simulation; Monomers; Neurodegenerative diseases; Organelles; protein-protein interactions; Proteins; Simulation; Static Electricity; Therapeutic targets; Tubulin; Tubulin - metabolism
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12020238

Microtubules are key players in several stages of the cell cycle and are also involved in the transportation of cellular organelles. Microtubules are polymerized by α/β tubulin dimers with a highly dynamic feature, especially at the plus ends of the microtubules. Therefore, understanding the interactions among tubulins is crucial for characterizing microtubule dynamics. Studying microtubule dynamics can help researchers make advances in the treatment of neurodegenerative diseases and cancer. In this study, we utilize a series of computational approaches to study the electrostatic interactions at the binding interfaces of tubulin monomers. Our study revealed that among all the four types of tubulin-tubulin binding modes, the electrostatic attractive interactions in the α/β tubulin binding are the strongest while the interactions of α/α tubulin binding in the longitudinal direction are the weakest. Our calculations explained that due to the electrostatic interactions, the tubulins always preferred to form α/β tubulin dimers. The interactions between two protofilaments are the weakest. Thus, the protofilaments are easily separated from each other. Furthermore, the important residues involved in the salt bridges at the binding interfaces of the tubulins are identified, which illustrates the details of the interactions in the microtubule. This study elucidates some mechanistic details of microtubule dynamics and also identifies important residues at the binding interfaces as potential drug targets for the inhibition of cancer cells.