Efficient internalization of TAT peptide in zwitterionic DOPC phospholipid membrane revealed by neutron diffraction

Xiaochao Chen, Shutao Liu, Bruno Deme, Viviana Cristiglio, Drew Marquardt, Richard Weller, Pingfan Rao, Yunqiang Wang, Jeremy Bradshaw

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

The aim of this study is to investigate the interactions between TAT peptides and a neutral DOPC bilayer by using neutron lamellar diffraction. The distribution of TAT peptides and the perturbation of water distribution across the DOPC bilayer were revealed. When compared to our previous study on an anionic DOPC/DOPS bilayer (X. Chen et al., Biochim Biophys Acta. 2013. 1828 (8), 1982–1988), a much deeper insertion of TAT peptides was found in the hydrophobic core of DOPC bilayer at a depth of 6.0 Å from the center of the bilayer, a position close to the double bond of fatty acyl chain. We conclude that the electrostatic attractions between the positively charged TAT peptides and the negatively charged headgroups of phospholipid are not essential for the direct translocation. Furthermore, the interactions of TAT peptides with the DOPC bilayer were found to vary in a concentration-dependent manner. A limited number of peptides first associate with the phosphate moieties on the lipid headgroups by using the guanidinium ions pairing. Then the energetically favorable water defect structures are adopted to maintain the arginine residues hydrated by drawing water molecules and lipid headgroups into the bilayer core. Such bilayer deformations consequently lead to the deep intercalation of TAT peptides into the bilayer core. Once a threshold concentration of TAT peptide in the bilayer is reached, a significant rearrangement of bilayer will happen and steady-state water pores will form.

Original languageEnglish
Pages (from-to)910-916
Number of pages7
JournalBiochimica et Biophysica Acta - Biomembranes
Volume1859
Issue number5
Early online date31 Jan 2017
DOIs
Publication statusE-pub ahead of print - 31 Jan 2017

Keywords

  • cell penetrating peptide
  • neutron diffraction
  • phospholipid
  • TAT peptide

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Cell Biology

Cite this

Efficient internalization of TAT peptide in zwitterionic DOPC phospholipid membrane revealed by neutron diffraction. / Chen, Xiaochao; Liu, Shutao; Deme, Bruno; Cristiglio, Viviana; Marquardt, Drew; Weller, Richard; Rao, Pingfan; Wang, Yunqiang; Bradshaw, Jeremy.

In: Biochimica et Biophysica Acta - Biomembranes, Vol. 1859, No. 5, 31.01.2017, p. 910-916.

Research output: Contribution to journalArticle

Chen, Xiaochao ; Liu, Shutao ; Deme, Bruno ; Cristiglio, Viviana ; Marquardt, Drew ; Weller, Richard ; Rao, Pingfan ; Wang, Yunqiang ; Bradshaw, Jeremy. / Efficient internalization of TAT peptide in zwitterionic DOPC phospholipid membrane revealed by neutron diffraction. In: Biochimica et Biophysica Acta - Biomembranes. 2017 ; Vol. 1859, No. 5. pp. 910-916.
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AU - Marquardt, Drew

AU - Weller, Richard

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AU - Wang, Yunqiang

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