» Articles » PMID: 10727239

Measurements of Interbilayer Forces and Protein Adsorption on Uncharged Lipid Bilayers Displaying Poly(ethylene Glycol) Chains

Overview
Journal Biochemistry
Specialty Biochemistry
Date 2000 Mar 22
PMID 10727239
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Poly(ethylene glycol) (PEG)-stabilized liposomes were recently shown to exhibit differences in cell uptake that were linked to the liposome charge. To determine the differences and similarities between charged and uncharged PEG-decorated liposomes, we directly measured the forces between two supported, neutral bilayers with terminally grafted PEG chains. The measurements were performed with the surface force apparatus. The force profiles were similar to those measured with negatively charged PEG conjugates of 1, 2-distearoyl-sn-glycero-3-phosphatidyl ethanolamine (DSPE), except that they lacked the longer ranged electrostatic repulsion observed with the charged compound. Theories for simple polymers describe the forces between end-grafted polymer chains on neutral bilayers. The force measurements were complemented by surface plasmon resonance studies of protein adsorption onto these layers. The lack of electrostatic forces reduced the adsorption of positively charged proteins and enhanced the adsorption of negatively charged ones. The absence of charge also allowed us to determine how membrane charge and the polymer grafting density independently affect protein adsorption on the coated membranes. Such studies suggest the physical basis of the different interactions of charged and uncharged liposomes with proteins and cells.

Citing Articles

Forces between mica and end-grafted statistical copolymers of sulfobetaine and oligoethylene glycol in aqueous electrolyte solutions.

Ahmed S, Leckband D J Colloid Interface Sci. 2021; 608(Pt 2):1857-1867.

PMID: 34752975 PMC: 9326957. DOI: 10.1016/j.jcis.2021.09.175.


Surface Plasmon Resonance as a Characterization Tool for Lipid Nanoparticles Used in Drug Delivery.

Chain C, Daza Millone M, Cisneros J, Ramirez E, Vela M Front Chem. 2021; 8:605307.

PMID: 33490037 PMC: 7817952. DOI: 10.3389/fchem.2020.605307.


Molecular Simulations of PEGylated Biomolecules, Liposomes, and Nanoparticles for Drug Delivery Applications.

Lee H Pharmaceutics. 2020; 12(6).

PMID: 32531886 PMC: 7355693. DOI: 10.3390/pharmaceutics12060533.


A Multiparametric and High-Throughput Assay to Quantify the Influence of Target Size on Phagocytosis.

Montel L, Pinon L, Fattaccioli J Biophys J. 2019; 117(3):408-419.

PMID: 31301802 PMC: 6697492. DOI: 10.1016/j.bpj.2019.06.021.


Insights into accelerated liposomal release of topotecan in plasma monitored by a non-invasive fluorescence spectroscopic method.

Fugit K, Jyoti A, Upreti M, Anderson B J Control Release. 2014; 197:10-9.

PMID: 25456833 PMC: 4356028. DOI: 10.1016/j.jconrel.2014.10.011.