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Polymers 2014, 6(3), 776-798; doi:10.3390/polym6030776
Abstract: Polyethylene glycol (PEG) has been conjugated to many drugs or drug carriers to increase their solubility and circulating lifetime, and reduce toxicity. This has motivated many experimental studies to understand the effect of PEGylation on delivery efficiency. To complement the experimental findings and uncover the mechanism that cannot be captured by experiments, all-atom and coarse-grained molecular dynamics (MD) simulations have been performed. This has become possible, due to recent advances in simulation methodologies and computational power. Simulations of PEGylated peptides show that PEG chains wrap antimicrobial peptides and weaken their binding interactions with lipid bilayers. PEGylation also influences the helical stability and tertiary structure of coiled-coil peptides. PEGylated dendrimers and single-walled carbon nanotubes (SWNTs) were simulated, showing that the PEG size and grafting density significantly modulate the conformation and structure of the PEGylated complex, the interparticle aggregation, and the interaction with lipid bilayers. In particular, simulations predicted the structural transition between the dense core and dense shell of PEGylated dendrimers, the phase behavior of self-assembled complexes of lipids, PEGylated lipids, and SWNTs, which all favorably compared with experiments. Overall, these new findings indicate that simulations can now predict the experimentally observed structure and dynamics, as well as provide atomic-scale insights into the interactions of PEGylated complexes with other molecules.
Polyethylene oxide (PEO) and polyethylene glycol (PEG) are polymers with the formulas, respectively, H3C–O–(CH2–CH2–O)n–CH3 and HO–(CH2–CH2–O)n–H, which have been widely used to replace various membranes, solvents, and nanocomposites for chemical, biomedical, and manufacturing applications. In particular, they have low toxicity and high solubility in water. Also, they can sterically shield molecules encapsulated in drug carriers and thus have been covalently or noncovalently conjugated to a number of pharmaceuticals, a process called PEGylation [1,2]. These biomedical applications of PEGylation have been shown to reduce the cytotoxicity as well as increase the water solubility and circulating lifetime of drug molecules or drug carriers such as peptides [3,4], oligonucleotides [5,6,7,8], lipid liposomes [9,10,11,12,13], biodegradable hydrogels [14,15] and nanoparticles [16,17,18,19]. Although experiments have revealed vital information on the large-scale interactions of PEGs with drugs and drug carriers, many atomic-level questions that cannot be answered by experiments remain to be solved. For example, the conformational and structural characterization of PEGylated complexes and their effects on delivery efficiency are not always easy to be interpreted by experiments. On the other hand, atomic-level phenomena can be captured in detail by molecular dynamics (MD) simulations, which offer insights into structure and dynamics, assuming that these simulations can be validated by successful comparisons to available experiment results. In particular, recent advances in computer performance and simulation methodology have allowed the direct comparison of simulation results with experiments, as well as visualization of the mechanism on atomic scale.
Simulation studies have been performed for various PEGylated molecules such as proteins, lipids, drugs, nanomaterials, hydrogels, and block copolymers. Since this field is too broad to be fully covered in this review, we here consider only selective computational studies: PEGylated antimicrobial peptides (AMPs), coiled-coil peptides, dendrimers, and single-walled carbon nanotubes (SWNTs), which have been widely simulated but relatively less reviewed. In this review, we will first (Section 2) briefly review the parameterization of all-atom and coarse-grained (CG) force fields for PEO and PEG. Next (Section 3), MD simulations of PEGylated AMPs and coiled-coil peptides will be reviewed. Lastly (Section 4 and Section 5), we will focus on simulations of PEGylated dendrimers and SWNTs.
2. Development of All-Atom and Coarse-Grained PEO/PEG Force Fields
Potential parameters, which typically consist of Lennard-Jones (LJ), electrostatic (coulomb), bond, angle, and torsional terms, have been developed for all-atom and coarse-grained (CG) PEO/PEG force fields. Quantum mechanics (QM) calculations were first performed and used for the development of all-atom models, which were again used to parameterize CG force fields. The details of potential parameters for each model are given in the references and will not be discussed in this review. Instead, the development history of some well-known PEG models will be briefly introduced.
The Smith group pioneered the development of the PEO/PEG model for the aqueous environment. The all-atom model for PEO was parameterized to reproduce relative free energies and conformer populations of 1,2-dimethoxyethane (DME) in water calculated from QM [20,21,22,23]. Their MD simulations captured the hydrogen bonding interaction between PEO and water, and predicted the conformational and structural properties of PEOs in water, in reasonable agreement with experiments [24,25]. Other groups also developed their own force fields and studied conformation and structure of short PEO and PEG chains [26,27,28,29,30,31]. Recently, MacKerell, Pastor, and coworkers developed the CHARMM ether force field (version C35) from the QM calculation , and then they corrected the torsional potential and released the revised version (C35r) . With the CHARMM C35r force field, MD simulations of 9-mers, 18-mers, 27-mers, and 36-mers of PEOs and PEGs showed the persistence length λ = 3.7 Å, the radii of gyration Rg ∝ Mw0.52 ± 0.02 (ideal chain behavior for short chains), hydrodynamic radii calculated from diffusivities, and the shape anisotropy of 2.59:1.44:1.00 , in excellent agreement with the polymer theories and experiments. Stepniewski et al. also parameterized PEGs with the OPLS all-atom force field and simulated the bilayer composed of PEGylated lipids, showing the electrostatic interaction between ions and PEG oxygens, and the penetration of PEGs into the hydrophobic region of the lipid bilayer in the liquid phase .
Although these all-atom models can accurately predict the conformation and structure of PEGs and their interactions with other molecules, their system size and time scale are limited. To overcome this, CG PEG models have also been developed. Initially, the implicit solvent models were developed by the Smith group and others, which predicted the experimentally observed chain dimensions, aggregation number, and critical micelle concentration [35,36,37]. Although not computationally demanding, the application of implicit solvent models to multicomponent mixtures is limited. For example, the implicit model cannot be used for the simulation of the complex with other molecules such as lipids and proteins. The CG PEO model with explicit solvent was developed by Klein and co-workers, showing the self-assembly of diblock copolymers in explicit water, and the strong interaction with lipid bilayers [38,39,40]. Our group parameterized a PEO/PEG model within a framework of the “MARTINI” CG force field developed by Marrink et al. [41,42]. The MARTINI PEO/PEG model predicted the size, diffusivities, hydrodynamics, end-to-end distances, and the distributions of bond lengths, angles, and dihedrals, all of which were close to those from all-atom simulations and experiments . In Figure 1, mixtures of lipids and PEGylated lipids in water self-assemble to liposomes, bicelles, and micelles at the expected ratios of lipids and PEGylated lipids [44,45], showing that the aggregate size decreases with increasing PEGylated-lipid concentration, in qualitative agreement with experiment. Recently, this CG model was reparameterized by the Monticelli group, which has an increased time step, while maintaining the accurate prediction of PEG conformation . Unlike other CG models, the CG model of mapping two monomers onto one bead was also developed .
3. Simulations of PEGylated Peptides
3.1. Antimicrobial Peptides
AMPs are short (<50 amino acids), cationic, and amphipathic peptides that can be extracted from eukaryotic organisms such as plants, insects, and vertebrates . Since cationic AMPs tend to interact electrostatically with anionic bacterial membranes rather than neutral animal membranes, they have been considered to be promising candidates for novel antibiotics [49,50]. To achieve this biomedical application, a high concentration of AMPs is required, but at high concentration they can also attack the human cell, indicating reduced specific targeting. To overcome this limitation, PEGylation has been applied to AMPs. Experimentally, nisin , magainin 2, and tachyplesin I [3,4] were PEGylated, showing increased solubility and decreased antimicrobial activity. In particular, the Matsuzaki group found that the decrease in antimicrobial activity was larger in β-sheet tachyplesin I than in α-helical magainin, showing the dependence on the peptide structure [3,4]. Most simulations and theoretical studies have focused on the secondary structure of AMPs and their interactions with lipid bilayers such as the formation of toroidal pores [52,53,54]. Here, simulations of PEGylated AMPs only will be reviewed.
Wu et al. performed all-atom simulations of cecropin P1 linked to the silica surface via a PEO chain, showing conformation of immobilized AMPs and their interactions with the silica surface . Recently, our group simulated PEGylated magainin 2 and tachyplesin I interacting with lipid bilayers . First, AMPs were simulated in water, showing that PEG chains wrap both magainin 2 and tachyplesin I. The α-helix of PEGylated magainin 2 was broken, while the β-sheet of PEGylated tachyplesin I remains stable, in agreement with experiments. Simulations of unPEGylated and PEGylated AMPs in lipid bilayers showed that PEGylation inhibits the electrostatic interaction between peptides and lipid head groups. Interestingly, this PEGylation effect was more significant for magainin 2 than for tachyplesin I because the random-coiled magainin 2 are more completely covered by PEG chains and thus cannot interact with the bilayer surface as much as tachyplesin I do (Figure 2), which qualitatively support Matsuzaki’s experiments.
3.2. Coiled-Coil Peptides
Coiled coils consist of two or more α-helices wound into a superhelix with a large pitch. The coiled-coil sequences contain a heptad repeat of seven amino acid residues, where hydrophobic residues are located in the core of coiled-coil helix bundles . Since these coiled coils can self-assemble into protein fibers, synthetic coiled coils have been designed and used as scaffolds in 3D cell culture engineering, as templates for the assembly of other polymer and nanoparticle materials, and as protein building blocks [58,59,60,61]. To increase their solubility and structural stability, coiled coils have been conjugated with PEGs. Experimentally, the Klok group [62,63,64,65,66], the Kros group [67,68,69,70,71], and the Xu group [72,73,74,75,76] synthesized PEGylated coiled coils, characterized their conformation and structure, and investigated the effect of PEGylation on the self-assembled structures and the interactions with other molecules. Computationally, the sequenced-based programs were developed to predict the existence and structure of coiled coils [77,78,79,80,81,82,83], and MD simulations were performed to study the stability of coiled coils [84,85,86,87,88,89,90,91,92,93].
Jain and Ashbaugh performed replica exchange MD (REMD) simulations of PEGylated coiled coils . PEG chains (20 and 40 monomers of EO; C–O–C) were conjugated to the N-terminal group of the lysine-rich peptide 1CW (pdb: 1COI, the peptide experimentally studied by the Xu group), the neutralized 1CW, and the polyalanine peptide. Figure 3 compares the fractional helicity of unPEGylated and PEGylated peptides as a function of temperature, indicating that larger PEG chains induce higher helicity of peptides, in quantitative agreement with experiments. Also, simulations showed that PEG chains have electrostatic interaction with cationic lysine residues of the peptide, which stabilizes the helical structure of each peptide but still does not influence the tertiary structure of the coiled coil.
Hamed et al. performed all-atom and CG simulations of the same α-helical peptide (pdb: 1COI) grafted with the PEG chain . Figure 4 shows that the PEG chain with a larger end-to-end distance induces an increase in the solvent accessible surface area (SASA) of the peptide, which makes the backbone hydrogen bonds more accessible to water molecules, leading to the lower helicity of the peptide. This indicates that peptide helicity is modulated by the SASA that depends on the PEG conformation and the PEG-peptide interaction. They also found that peptides interact with PEG chains because of the electrostatic interaction between cationic lysines and PEG oxygens as well as the interaction of hydrophobic amino acids with PEGs rather than with water.
Besides these coiled coils, the self-assemblies of cyclic peptides grafted with PEG chains were recently simulated by Ruiz and Keten . They calculated the binding free energies for a cyclic peptide dimer with and without PEGs, showing that the binding energy between peptides is modulated by the PEG length and grafting density. Their findings also agree with theories and experimental observations that showed the entropic penalty induced by the conformational transition of the conjugated PEG chains in assembled nanotubes.
4. Simulations of PEGylated Dendrimers
Polyamidoamine (PAMAM) dendrimers, which consist of a central core, regularly branched monomeric building blocks, and many surface terminal groups, are among the best candidate nanoparticles for use as antitumor therapeutics to detect and target tumor cells because of their controlled mass, surface valency, and surface functionality . The conformation and structure of PAMAM dendrimers and their interactions with conjugate molecules (DNA, peptides, and polymers) and lipid bilayers have been widely studied through experiments and simulations [98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129]. Here, the simulation studies on PEGylated dendrimers are reviewed.
Tanis and Karatasos performed all-atom MD simulations of a dendrimer grafted with a single PEO chain and predicted the complex conformation and the extent of the hydrogen bonds between dendrimer and PEO at various pH values . Our group performed CG MD simulations of PEGylated dendrimers, showing the inhibition effect of PEG chains on the interparticle aggregation in water  and on the dendrimer-induced pore formation in lipid bilayers . In particular, we simulated generations 3, 4, and 5 dendrimers grafted with PEGs of different sizes (Mw = 550 and 5000) and grafting densities (12%–94% of surface terminals), showing that longer PEG chains with higher grafting density yield PEG–PEG crowding, which stretches dendrimer terminals towards water, leading to a larger size and a dense-shell structure of the dendrimer , as shown in Figure 5. Also, simulations showed that long PEG5000 chains at high grafting density self-penetrate into the attached dendrimer, occupying the dendrimer’s vacant interior that would otherwise be available for encapsulating hydrophobic compounds, implying that the encapsulation efficiency of dendrimers can be modulated by the PEG length and grafting density.
Albertazzi et al. synthesized hybrid dendrimers with PEG cores , which are different from other PEGylated dendrimers that typically have PEG chains grafted onto outer terminal groups. Their experiments showed that the extent of cellular uptake and transfection is modulated by the complex structure and the topology of the PEG core. These results were supported by their MD simulations of dendrimers with 2-arm PEG cores and 4-arm PEG cores, which showed that the dendrimers with more PEG cores have a much more swollen conformation, as shown in Figure 6.
Recently, Karatasos simulated PEGylated hyperbranched polyesters with doxorubicin (a hydrophobic anti-cancer drug) . Figure 7 shows that PEGylated polyesters form a complex with doxorubicin via their hydrogen bonding interactions. These hydrogen bonding interactions were modulated by the charge density of doxorubicin and the size of PEG chains, indicating the dependence on drug electrostatics and PEG conformation.
Pavan et al. performed well-tempered metadynamics simulations of PEGylated dendrimers in water to obtain enough samples by overcoming energy barriers . Radii of gyration and hydrodynamic radii of PEGylated dendrimers were calculated, in excellent agreement with those measured from their dynamic light scattering (DLS) experiments. The free energy surface of PEGylated dendrimers in water indicated that PEGylated dendrimers have a tight globular shape rather than an open configuration. They also found that larger PEGs induce a higher extent of crowding, leading to aggregation of the dendrimer-PEG complex.
5. Simulations of PEGylated Carbon Nanotubes
SWNTs have been considered to be promising nanomaterials for use as antitumor therapeutics and drug or gene transporters because of their excellent mechanical strength and chemical stability [137,138,139]. However, SWNTs are highly hydrophobic and thus aggregate in aqueous environment, which limits their biomedical applications in vivo. To overcome this, SWNTs have been covalently conjugated with PEG chains or noncovalently assembled with PEGylated lipids or surfactants. Experiments have shown (or proposed) the self-assembled structures of the SWNT-PEG complex, the conformation of the grafted PEG chains, the effect of PEGylation on SWNT aggregation, and the interaction of PEGylated SWNTs with lipid bilayers [140,141,142,143,144,145,146,147,148,149], which have motivated simulation studies.
Computational studies have mainly focused on the self-assembly of SWNTs and surfactants (or lipids) [143,150,151,152,153,154], and the interaction between SWNTs and lipid bilayers [155,156,157,158,159,160,161,162,163,164,165,166,167,168]. Simulations have shown that the self-assembly of SWNTs and their interactions with lipid bilayers can be modulated by the structure and concentration of surfactant, and the size and chirality of SWNT. To simulate PEGylated SWNTs and their interactions with lipid bilayers, our group recently parameterized CG SWNT and its interaction with CG PEG within a framework of the MARTINI force field . We simulated the mixtures of SWNTs and lipids (or PEGylated lipids), which visualized the experimentally observed (or proposed) structures of the self-assembled SWNT-lipid complex. In Figure 8, lysophospholipids (single tail per lipid), phospholipids (double tails per lipid), and PEGylated phospholipids adsorb onto SWNTs in different conformations as “helical half-cylinders”, “cylindrical micelles”, and “hemimicelles (or random-adsorption)”, respectively. These simulation findings indicate the dependence on the size of the lipid headgroup and tail, indicating the effects of lipid types and PEGylation, implying important roles of PEGylation and lipid types on the self-assembled structure and mechanism, which favorably compared with experimental findings.
To understand the effects of PEGylation on interparticle aggregation, we also simulated multiple copies of the SWNT-lipid complex in water . Figure 9 shows that all pure SWNTs aggregate, lipid-wrapped SWNTs partially aggregate, but PEGylated lipid-wrapped SWNTs completely disperse, indicating that short PEG chains (Mw = 550) can inhibit interparticle aggregation, in agreement with experiment.
The interactions between SWNTs and lipid bilayers were also investigated [170,171]. Un-PEGylated SWNTs insert into the lipid bilayer at the beginning of the simulation because of the hydrophobic interaction with the bilayer tails, while PEGylated SWNTs do not for the whole simulation time, indicating that long hydrophilic PEG chains can weaken the hydrophobic interaction and inhibit SWNT insertion (Figure 10). For unPEGylated SWNTs, the inserted SWNT beads are surrounded by entire tails of neighboring lipids in one leaflet of the bilayer, which induces positive curvature along the SWNT. This indicates that the insertion of SWNT into the bilayer and membrane curvature can be modulated by PEGylation. Our simulations also found that the PEGylation method influences the distribution of PEG chains along the SWNT, and that PEG size and grafting density modulate the conformation of PEG chains on SWNTs , which supports the experimentally proposed conformation of PEGs  and compares favorably with the mushroom-brush transition of the Alexander-de Gennes theory .
Recently, Crescenzo et al. performed all-atom MD simulations of SWNTs grafted with PEGs (homopolymer) and PEG-propylene sulfide (PEG-PPS; block copolymer), and compared the extent of covering the SWNT surface, showing that PEG-PPS more tightly wrap SWNTs than pure PEG do . Aslan et al. simulated the self-assembly of PEGylated lipids and either an isolated or bundled SWNT, showing different density profiles of PEGs and their effects on antimicrobial activity . Skandani and Al-Haik performed all-atom MD simulations of unPEGylated and PEGylated SWNTs with different diameters and chiralities in lipid bilayers . Simulations showed that PEGylated SWNTs penetrated into the lipid bilayer slower than unPEGylated SWNTs. Also, penetration of the PEGylated SWNT showed a less energy-dependent mechanism, indicating lower adhesion energy, which favorably compared with their previous experiments .
Recent advances in simulation methodologies and computational power have made it possible to accurately predict conformation and dynamics. The all-atom models for PEO and PEG have been parameterized to reproduce free energies and conformer populations calculated from quantum chemistry calculations, which were again used to parameterize CG models. Initially, implicit solvent models were developed, but the explicit solvent models have become more popular, since they can be easily applied to multicomponent mixtures. All-atom and CG models predicted the conformation, hydrodynamics, and shape anisotropy of PEO and PEG, in excellent agreement with experiments and polymer theories. In particular, the CG models have been applied to large-scale systems such as the self-assembly of PEG and other molecules, and the interaction with lipid bilayers.
MD simulations have revealed much useful information about the structure and dynamics of PEGylated molecules. Since PEG chains are hydrophilic, they have been shown to have either attractive interactions with charged or hydrophilic molecules or repulsive interactions with highly hydrophobic molecules. For example, antimicrobial peptides, which consist of cationic amino acids, are wrapped by PEG chains. Also, PEG chains adsorb onto coiled coils that form helix bundles because of the core packing with hydrophobic residues and the electrostatic interaction between charged residues. All-atom simulations showed that the stability of secondary and tertiary structures of these peptides is modulated by PEGylation, implying the possible application of PEGylation into the peptide-based drugs and nanofibers. PEGylated nanoparticles such as dendrimers and SWNTs have also been computationally studied. Simulations of PEGylated dendrimers showed that the PEG size and grafting density influence the size, shape, and structural transition between the dense core and dense shell. Also, PEGylation inhibits the interparticle aggregation of dendrimers and weakens the interaction between dendrimers and lipid bilayers. For PEGylated lipids, CG simulations captured the self-assembled liposomes, bicelles, and micelles at the expected ratios of lipids and PEGylated lipids. The conformations of PEG chains grafted onto SWNTs, and the structures of the self-assembled SWNT-lipid (or PEGylated lipid) complex, the effects of PEGylation on interparticle aggregation and the interaction with lipid bilayers were favorably compared with polymer theories and experiments.
As reviewed above, all-atom and CG MD simulations have successfully matched experimentally measured properties and have provided atomic-scale insights into the structure and dynamics of PEG and its interactions with other molecules. However, more computational studies are still needed to complement or explain experimental observations. For example, different mechanisms for the penetration of polymers and nanoparticles into cell membranes have been proposed but are still not well understood. Also, simulations with ions have always been challenging due to force-field issues. For peptide simulation, the secondary structure and folding state need to be more accurately predicted within the limited simulation timescale. To resolve this in the future, advances in force field and simulation methodology should be attempted. This information from simulations can help in optimizing the size and grafting density of PEG chains to increase drug-delivery efficiency for applications in nanomedicine.
This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2012R1A1A1001196).
Conflicts of Interest
The authors declare no conflict of interest.
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