Volume 8, Issue 3
Influences of Cell-Penetrating Peptide Concentration on the Penetration of Phospholipid Membrane

Qi Wu, Kun Wu & Qing-Tian Meng

J. At. Mol. Sci., 8 (2017), pp. 141-145.

Published online: 2017-08

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  • Abstract

It is necessary to fully understand the interaction between the cell penetration peptide and the different types of phospholipid membranes. In this research the interaction between R9 antibacterial peptide and asymmetric phospholipid is studied by using the method of coarse-grained dynamic simulation. The investigation shows that when there is only one R9 antibacterial peptide in the system, it is hard to penetrate through the phospholipid membrane spontaneously. When the concentration of the antibacterial peptide reaches a certain value, with the help of the enhanced electrostatic interactions and the cooperative effect, the peptides will pass through the phospholipid bilayer and reach the inside of the cell. Increasing the concentration of antimicrobial peptides is helpful to improve the penetration rate of the peptides. Our results can provide some theoretical guidance for drug delivery in the biological system.

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COPYRIGHT: © Global Science Press

  • Email address

qtmeng@sdnu.edu.cn (Qing-Tian Meng)

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@Article{JAMS-8-141, author = {Wu , QiWu , Kun and Meng , Qing-Tian}, title = {Influences of Cell-Penetrating Peptide Concentration on the Penetration of Phospholipid Membrane}, journal = {Journal of Atomic and Molecular Sciences}, year = {2017}, volume = {8}, number = {3}, pages = {141--145}, abstract = {

It is necessary to fully understand the interaction between the cell penetration peptide and the different types of phospholipid membranes. In this research the interaction between R9 antibacterial peptide and asymmetric phospholipid is studied by using the method of coarse-grained dynamic simulation. The investigation shows that when there is only one R9 antibacterial peptide in the system, it is hard to penetrate through the phospholipid membrane spontaneously. When the concentration of the antibacterial peptide reaches a certain value, with the help of the enhanced electrostatic interactions and the cooperative effect, the peptides will pass through the phospholipid bilayer and reach the inside of the cell. Increasing the concentration of antimicrobial peptides is helpful to improve the penetration rate of the peptides. Our results can provide some theoretical guidance for drug delivery in the biological system.

}, issn = {2079-7346}, doi = {https://doi.org/10.4208/jams.102817.121817a}, url = {http://global-sci.org/intro/article_detail/jams/12557.html} }
TY - JOUR T1 - Influences of Cell-Penetrating Peptide Concentration on the Penetration of Phospholipid Membrane AU - Wu , Qi AU - Wu , Kun AU - Meng , Qing-Tian JO - Journal of Atomic and Molecular Sciences VL - 3 SP - 141 EP - 145 PY - 2017 DA - 2017/08 SN - 8 DO - http://doi.org/10.4208/jams.102817.121817a UR - https://global-sci.org/intro/article_detail/jams/12557.html KW - AB -

It is necessary to fully understand the interaction between the cell penetration peptide and the different types of phospholipid membranes. In this research the interaction between R9 antibacterial peptide and asymmetric phospholipid is studied by using the method of coarse-grained dynamic simulation. The investigation shows that when there is only one R9 antibacterial peptide in the system, it is hard to penetrate through the phospholipid membrane spontaneously. When the concentration of the antibacterial peptide reaches a certain value, with the help of the enhanced electrostatic interactions and the cooperative effect, the peptides will pass through the phospholipid bilayer and reach the inside of the cell. Increasing the concentration of antimicrobial peptides is helpful to improve the penetration rate of the peptides. Our results can provide some theoretical guidance for drug delivery in the biological system.

Qi Wu, Kun Wu & Qing-Tian Meng. (2019). Influences of Cell-Penetrating Peptide Concentration on the Penetration of Phospholipid Membrane. Journal of Atomic and Molecular Sciences. 8 (3). 141-145. doi:10.4208/jams.102817.121817a
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