Steered Molecular Dynamics Simulations of a Type IV Pilus Probe Initial Stages of a Force-Induced Conformational Transition

被引:17
作者
Baker, Joseph L. [1 ]
Biais, Nicolas [2 ]
Tama, Florence [3 ]
机构
[1] Univ Arizona, Dept Phys, Tucson, AZ 85721 USA
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[3] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
TOXIN-COREGULATED PILUS; NEISSERIA-GONORRHOEAE; PSEUDOMONAS-AERUGINOSA; EPITHELIAL-CELLS; RECEPTOR-BINDING; PILIN; ADHESION; CYTOPROTECTION; RESOLUTION; MICROSCOPY;
D O I
10.1371/journal.pcbi.1003032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Type IV pili are long, protein filaments built from a repeating subunit that protrudes from the surface of a wide variety of infectious bacteria. They are implicated in a vast array of functions, ranging from bacterial motility to microcolony formation to infection. One of the most well-studied type IV filaments is the gonococcal type IV pilus (GC-T4P) from Neisseria gonorrhoeae, the causative agent of gonorrhea. Cryo-electron microscopy has been used to construct a model of this filament, offering insights into the structure of type IV pili. In addition, experiments have demonstrated that GC-T4P can withstand very large tension forces, and transition to a force-induced conformation. However, the details of force-generation, and the atomic-level characteristics of the force-induced conformation, are unknown. Here, steered molecular dynamics (SMD) simulation was used to exert a force in silico on an 18 subunit segment of GC-T4P to address questions regarding the nature of the interactions that lead to the extraordinary strength of bacterial pili. SMD simulations revealed that the buried pilin alpha 1 domains maintain hydrophobic contacts with one another within the core of the filament, leading to GC-T4P's structural stability. At the filament surface, gaps between pilin globular head domains in both the native and pulled states provide water accessible routes between the external environment and the interior of the filament, allowing water to access the pilin alpha 1 domains as reported for VC-T4P in deuterium exchange experiments. Results were also compared to the experimentally observed force-induced conformation. In particular, an exposed amino acid sequence in the experimentally stretched filament was also found to become exposed during the SMD simulations, suggesting that initial stages of the force induced transition are well captured. Furthermore, a second sequence was shown to be initially hidden in the native filament and became exposed upon stretching.
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页数:12
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