Isolated polar amino acid residues modulate lipid binding in the large hydrophobic cavity of CD1d

Shinsuke Inuki, Toshihiko Aiba, Natsumi Hirata, Osamu Ichihara, Daisuke Yoshidome, Shunsuke Kita, Katsumi Maenaka, Koichi Fukase, Yukari Fujimoto

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The CD1d protein is a nonpolymorphic MHC class I-like protein that controls the activation of natural killer T (NKT) cells through the presentation of self- and foreign-lipid ligands, glycolipids, or phospholipids, leading to the secretion of various cytokines. The CD1d contains a large hydrophobic lipid binding pocket: the A′ pocket of CD1d, which recognizes hydrophobic moieties of the ligands, such as long fatty acyl chains. Although lipid-protein interactions typically rely on hydrophobic interactions between lipid chains and the hydrophobic sites of proteins, we showed that the small polar regions located deep inside the hydrophobic A′ pocket could be used for the modulation of the lipid binding. A series of the ligands, α-galactosyl ceramide (α-GalCer) derivatives containing polar groups in the acyl chain, was synthesized, and the structure-activity relationship studies demonstrated that simple modification from a methylene to an amide group in the long fatty acyl chain, when introduced at optimal positions, enhanced the CD1d recognition of the glycolipid ligands. Formation of hydrogen bonds between the amide group and the polar residues was supported by molecular dynamics (MD) simulations and WaterMap calculations. The computational studies suggest that localized hydrating water molecules may play an important role in the ligand recognition. Here, the results showed that confined polar residues in the large hydrophobic lipid binding pockets of the proteins could be potential targets to modulate the affinity for its ligands.

Original languageEnglish
Pages (from-to)3132-3139
Number of pages8
JournalACS Chemical Biology
Volume11
Issue number11
DOIs
Publication statusPublished - 2016 Nov 18

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Ligands
Lipids
Amino Acids
Glycolipids
Proteins
Amides
Galactosylceramides
Cold Climate
Natural Killer T-Cells
T-cells
Molecular Dynamics Simulation
Structure-Activity Relationship
Hydrophobic and Hydrophilic Interactions
Molecular dynamics
Hydrogen
Phospholipids
Carrier Proteins
Hydrogen bonds
Chemical activation
Modulation

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine

Cite this

Isolated polar amino acid residues modulate lipid binding in the large hydrophobic cavity of CD1d. / Inuki, Shinsuke; Aiba, Toshihiko; Hirata, Natsumi; Ichihara, Osamu; Yoshidome, Daisuke; Kita, Shunsuke; Maenaka, Katsumi; Fukase, Koichi; Fujimoto, Yukari.

In: ACS Chemical Biology, Vol. 11, No. 11, 18.11.2016, p. 3132-3139.

Research output: Contribution to journalArticle

Inuki, S, Aiba, T, Hirata, N, Ichihara, O, Yoshidome, D, Kita, S, Maenaka, K, Fukase, K & Fujimoto, Y 2016, 'Isolated polar amino acid residues modulate lipid binding in the large hydrophobic cavity of CD1d', ACS Chemical Biology, vol. 11, no. 11, pp. 3132-3139. https://doi.org/10.1021/acschembio.6b00674
Inuki, Shinsuke ; Aiba, Toshihiko ; Hirata, Natsumi ; Ichihara, Osamu ; Yoshidome, Daisuke ; Kita, Shunsuke ; Maenaka, Katsumi ; Fukase, Koichi ; Fujimoto, Yukari. / Isolated polar amino acid residues modulate lipid binding in the large hydrophobic cavity of CD1d. In: ACS Chemical Biology. 2016 ; Vol. 11, No. 11. pp. 3132-3139.
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