Molecular mechanisms of integrin αvβ8 activation regulated by graphene, boron nitride and black phosphorus nanosheets

Zhenyu Liao, Xinyao Ma, Ji-Jung Kai, Jun Fan*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

5 Citations (Scopus)

Abstract

Integrin αvβ8 is a heterodimeric transmembrane protein on macrophages. Nanosheets can activate the integrin and elicit immune responses, exhibiting adverse immunotoxicity. Understanding the mechanism of integrin activation regulated by nanosheets is crucial for safe and effective use of nanosheets in biomedical applications. Herein, we performed all-atom molecular dynamics simulations to clarify the interactions between integrin αvβ8 in the cell membrane and three types of nanosheets, graphene (GRA), hexagonal boron nitride (BN), and black phosphorus (BP). We observed that BP could adsorb the intracellular end of αv monomer and thus break the inner membrane clasp, an important hydrophobic cluster for maintaining the inactive state of integrin. The association between αv and β8 subunit is weakened, promoting the integrin activation. By contrast, GRA and BN exert little influence on the association state of the integrin. Interestingly, the puckered structure of BP affects the integrin activation, where BP with the armchair direction perpendicular to the membrane plane cannot unpack the integrin. Moreover, the perturbation effect of nanosheets on the membrane was also evaluated. BP shows a milder effect on membrane structures and lipid properties than GRA and BN. This work unravels the molecular basis on the activation of integrin mediated by three nanosheets, and suggests the toxicity and therapeutic effect of well-established nanomaterials in the immune system. © 2023 Elsevier B.V.
Original languageEnglish
Article number113139
JournalColloids and Surfaces B: Biointerfaces
Volume222
Online published11 Jan 2023
DOIs
Publication statusPublished - Feb 2023

Funding

This work was supported by the Research Grant Council of Hong Kong under Grants Nos. 11306517, 11305919 and 11308620, NSFC/RGC Joint Research Scheme N_CityU104/19, and the computing resources of the X-GPU cluster supported by the Hong Kong Research Grant Council Collaborative Research Fund: C6021-19EF. This project was also supported by CLP Power Hong Kong under grants 9229033 to Prof. JJ Kai.

Research Keywords

  • 2D nanomaterial
  • Anisotropy
  • Immune response
  • Integrin
  • Molecular dynamics simulation

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