AI Article Synopsis

  • Flagellum is a whip-like appendage in single-celled organisms that has a complex structure made of flagellin consisting of various domains.
  • The study investigates how the D3 residues of flagellin interact with two types of single-walled carbon nanotubes (SWNT) - metallic and semiconducting - using molecular dynamics simulations.
  • Findings reveal that metallic SWNTs have stronger interactions with glycine and threonine residues, while semiconducting SWNTs predominantly interact with areas of the protein lacking glycine, highlighting the importance of glycine in differentiating between the two types of nanotubes.

Article Abstract

Flagellum is a lash-like cellular appendage found in many single-celled living organisms. The flagellin protofilaments contain 11-helix dual turn structure in a single flagellum. Each flagellin consists of four sub-domains - two inner domains (D0, D1) and two outer domains (D2, D3). While inner domains predominantly consist of α-helices, the outer domains are primarily beta sheets with D3. In flagellum, the outermost sub-domain is the only one that is exposed to the native environment. This study focuses on the interactions of the residues of D3 of an R-type flagellin with 5nm long chiral (5,15) and arm-chair (12,12) single-walled carbon nanotubes (SWNT) using molecular dynamics simulation. It presents the interactive forces between the SWNT and the residues of D3 from the perspectives of size and chirality of the SWNT. It is found that the metallic (arm-chair) SWNT interacts the most with glycine and threonine residues through van der Waals and hydrophobic interactions, whereas the semiconducting (chiral) SWNT interacts largely with the area of protein devoid of glycine by van der Waals, hydrophobic interactions, and hydrogen bonding. This indicates a crucial role that glycine plays in distinguishing metallic from semiconducting SWNTs.

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Source
http://dx.doi.org/10.1109/TCBB.2015.2459696DOI Listing

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