Photocleavable Poly Research Articles

Dynamic cell photo-manipulation technology for the molecular and mechanical regulation analyses of collective cell migration

Collective cell migration is an essential biological process. Migration behaviors of multiple cellular units depend on the mechanical and chemical properties of their scaffolds and the geometry of the cells. However, the mechanisms by which these properties synergistically regulate the collective cell characteristics remain unknown. A robust method is required to analyze collective cell migration. Therefore, in this study, we developed a new method for collective cell migration analysis using defined chemical, mechanical, and geometrical properties. Our method is based on a poly(acrylic acid) hydrogel, whose surface is functionalized with photocleavable poly(ethylene glycol) and a cell-adhesive peptide. By controlling the UV irradiation of the photoactivatable hydrogel, we created geometrically controlled cellular clusters and induced collective migration. Furthermore, chemical and mechanical cues exposed to cell clusters were manipulated depending on the surface density of the cell-adhesive peptide and crosslinking density of the hydrogel. As a proof of concept, we also demonstrated that the collective migration of epithelial cells was synergistically regulated by the chemical and mechanical properties of the scaffold. Our results suggest the new photoactivatable substrate as a promising tool for advanced molecular and mechanobiological analyses of collective cell migration.

Enzyme-Polymer Conjugates with Photocleavable Linkers for Control Over Protein Activity.

Reversible conjugation of polymers to proteins is important for a variety of applications, for example to control protein activity. Light is often employed as an external trigger to allow for spatio and temporal control over release of a payload. In this report, we demonstrate preparation of photocleavable poly(polyethylene glycol) acrylate)-lysozyme (pPEGA-Lys) conjugates via ortho-nitrobenzyl linkages. The conjugates were made by both grafting-to and grafting-from in order to compare and contrast the two synthetic approaches. First, a lysine-reactive ortho-nitrobenzyl atom transfer radical polymerization (ATRP) initiator was synthesized. For the grafting-to strategy, the initiator was employed in the ATRP of PEGA, and the subsequent polymer was conjugated to the lysine residues of lysozyme. For the grafting-from strategy, lysozyme was modified first with the photocleavable initiator, and the purified macroinitiator was then subjected to polymerization conditions to synthesize the protein-polymer conjugate. The polymer was cleaved from the protein via UV light, and activity before and after polymer removal was evaluated, showing 83% recovery. This work provides evidence that reversing conjugation is successful for activity modulation for ortho-nitrobenzyl linked protein-polymer conjugates.

Synthesis, and characterization folate-conjugated photocleavable poly(4-substituted-ε-caprolactone) polymers for drug delivery

Photo-cleavable polymers containing 5-hydroxy-2-nitrobenzyl alcohol (ONB) junction point between the target molecule of folic acid (FA) and the hydrophobic poly(4-substituted-ɛ-caprolactone) (PXCLn) chain were synthesized. FA –terminated ONB-PXCLn polymers formed micelles with critical micelle concentration (CMC) 1.2 – 64.3 mg L−1. Fluorescence emission spectroscopy indicated the release of Nile red encapsulated FA-ONB-PXCLn micelles in response to irradiation. Light-triggered bursts released were observed for drug-loaded FA-ONB-PXCLn micelles. The nanoparticles exhibited nonsignificant toxicity at concentrations up to 300 µg mL−1. Flow cytometry revealed that the uptake of folate-targeted doxorubicin (DOX) -encapsulated micelles by HeLa cells was faster than that of free DOX.

Photoactivatable Hydrogel Interfaces for Resolving the Interplay of Chemical, Mechanical, and Geometrical Regulation of Collective Cell Migration

Collective migration is the mechanobiological interplay within migrating cell clusters and against extracellular matrixes (ECMs) underneath, mediating various physiological and pathological processes. Therefore, it is crucial to develop a robust platform on which collective migration can be studied under standardized conditions to understand how cells migrate differently between normal and disease states. We herein demonstrated phtotoactivatable hydrogel interfaces as suitable candidates for such applications. The substrate was composed of a poly(acrylamide) (PAAm) hydrogel whose surface was sequentially functionalized with poly-d-lysine (PDL) and photocleavable poly(ethylene glycol) (PEG). On the surface of the gel substrates, cell clusters with any given geometries can be prepared by controlling the irradiation patterns (geometrical cue), and their collective migration can be induced by the subsequent irradiation of the surrounding regions. Moreover, the substrate mechanical properties can be controlled by changing the composition of the PAAm hydrogel (mechanical cue), and the chemical properties were controlled by changing the amount of immobilized PDL, thereby altering the adsorbed amount of ECM proteins (chemical cue). The photoactivatable gel substrates were characterized by fluorescence microscopy, ζ-potential measurements, and the protein adsorption test. Through the study of the interplay of chemical, mechanical, and geometrical cues in the regulation of collective characteristics, we found additive effects of chemical and mechanical cues on the suppression of circular expansion by up-regulating the epithelial morphology. Also, the impact of geometrical cues became more significant by decreasing the chemical cue. We believe the present platform will be a useful research tool for the comprehensive mechanobiological analysis of collective cell migration.

Photocleavable and tunable thermoresponsive amphiphilic random copolymer: Self‐assembly into micelles, dye encapsulation, and triggered release

ABSTRACTA double‐responsive amphiphilic random copolymer (P(OEtOxA)‐ran‐PNBA) composed of thermoresponsive poly(oligo(2‐ethyl‐2‐oxazoline)acrylate) (P(OEtOxA)) segments and photocleavable poly(2‐nitrobenzyl acrylate) (PNBA) segments is synthesized via combination of cationic ring‐opening polymerization (CROP) and reversible addition‐fragmentation chain transfer (RAFT) polymerization techniques. The P(OEtOxA)‐ran‐PNBA copolymer exhibits lower critical solution (LCST)‐type soluble‐to‐turbid phase transition in water with tunable cloud point (Tcp) with respect to chain length of P(OEtOxA) segment present. The photocleavage of PNBA segments by UV irradiation transforms amphiphilic P(OEtOxA)‐ran‐PNBA to fully hydrophilic P(OEtOxA)‐ran‐poly(acrylic acid) resulting in the appreciable increase of Tcp of copolymer in aqueous solution. Owing to the amphiphilic nature, the P(OEtOxA)‐ran‐PNBA copolymer molecules self‐assemble into well‐dispersed spherical micelles in water. There is a disruption of the copolymer micelles with UV light irradiation as well as shrinkage of micellar size with increasing temperature above the LCST of copolymer in solution. Finally, the encapsulation of hydrophobic guest molecule (nile red) into P(OEtOxA)‐ran‐PNBA copolymer micelles and thermo‐ and photo‐triggered release of nile red are demonstrated. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 1714–1729

Synthesis and Self-Aggregation of Poly(2-ethyl-2-oxazoline)-Based Photocleavable Block Copolymer: Micelle, Compound Micelle, Reverse Micelle, and Dye Encapsulation/Release

We report on the synthesis of photocleavable poly(2-ethyl-2-oxazoline)-block-poly(2-nitrobenzyl acrylate) (PEtOx-b-PNBA) block copolymers (BCPs) with varying compositions via combination of microwave-assisted cationic ring-opening polymerization (CROP) and atom transfer radical polymerization (ATRP) using α-bromoisobutyryl bromide as an orthogonal initiator. The amphiphilic nature of this BCP causes them to self-assemble into primary micelles in THF/H2O, which further undergo secondary aggregation into nanostructured compound micelles as established through DLS, FESEM, and TEM. Upon UV irradiation (λ = 350 nm), the photocleavage of the PNBA block of the PEtOx-b-PNBA BCP takes place, and that leads to the formation of the doubly hydrophilic poly(2-ethyl-2-oxazoline)-b-poly(acrylic acid) (PEtOx-b-PAA) BCP causing the rupture of compound micelles as confirmed by spectroscopic and microscopic techniques. Encapsulation of a model hydrophobic guest molecule, nile red (NR), into the photocleavable BCP micellar core in aqueous solution and its UV-induced release is also investigated by fluorescence emission measurements. PEtOx-b-PNBA BCP amphiphiles are also shown to self-assemble into spherical nanostructures (∼90 nm) in dichloromethane as established by DLS and TEM analysis. These are referred to as reverse micelles and are able to encapsulate anionic hydrophilic dye, Eosin B, and facilitate its solubilization in organic media.

Synthesis and crystallization of star‐shaped photocleavable poly(ε‐caprolactone)s

ABSTRACTHere, we report on the synthesis and different crystallization behavior of linear‐ and star‐ PCL's containing a photocleavable linker (5‐hydroxy‐2‐nitro benzaldehyde), modulated by photochemical switching. Basis is the attachment of a photocleavable moiety close to the star‐core of a three‐arm star poly(caprolactone), so that the crystallization behavior can be controlled via a photochemical stimulus. The polymerization of ε‐caprolactone using a trivalent photocleavable initiator and stannous octanoate catalyst resulted in the synthesis of different molecular weights of star‐shaped photocleavable polymers. Various techniques like 1H NMR and ESI‐TOF‐MS confirmed the successful synthesis of the star‐shaped polymers. Complete photocleavage is ensured via GPC, HPLC, and ESI‐TOF‐MS. DSC studies clearly indicated the enhancement in crystallinity after photocleavage of the star‐shaped poly(ε‐caprolactone)s. Hence, for the first time phototriggered crystallization behavior of PCL polymers is reported, where the confinement exerted by the star architecture is removed by photoirradiation. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 642–649

A Photoactivatable Nanopatterned Substrate for Analyzing Collective Cell Migration with Precisely Tuned Cell-Extracellular Matrix Ligand Interactions

Collective cell migration is involved in many biological and pathological processes. Various factors have been shown to regulate the decision to migrate collectively or individually, but the impact of cell-extracellular matrix (ECM) interactions is still debated. Here, we developed a method for analyzing collective cell migration by precisely tuning the interactions between cells and ECM ligands. Gold nanoparticles are arrayed on a glass substrate with a defined nanometer spacing by block copolymer micellar nanolithography (BCML), and photocleavable poly(ethylene glycol) (Mw = 12 kDa, PEG12K) and a cyclic RGD peptide, as an ECM ligand, are immobilized on this substrate. The remaining glass regions are passivated with PEG2K-silane to make cells interact with the surface via the nanoperiodically presented cyclic RGD ligands upon the photocleavage of PEG12K. On this nanostructured substrate, HeLa cells are first patterned in photo-illuminated regions, and cell migration is induced by a second photocleavage of the surrounding PEG12K. The HeLa cells gradually lose their cell-cell contacts and become disconnected on the nanopatterned substrate with 10-nm particles and 57-nm spacing, in contrast to their behavior on the homogenous substrate. Interestingly, the relationship between the observed migration collectivity and the cell-ECM ligand interactions is the opposite of that expected based on conventional soft matter models. It is likely that the reduced phosphorylation at tyrosine-861 of focal adhesion kinase (FAK) on the nanopatterned surface is responsible for this unique migration behavior. These results demonstrate the usefulness of the presented method in understanding the process of determining collective and non-collective migration features in defined micro- and nano-environments and resolving the crosstalk between cell-cell and cell-ECM adhesions.

Functionalized Stimuli-Responsive Nanocages from Photocleavable Block Copolymers

The light-induced formation of pH and temperature-responsive poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) nanocages is demonstrated here. The strategy is based on the self-assembly in aqueous solutions of a photocleavable poly(tert-butyl acrylate)-hv-poly[2-(dimethylamino)ethyl methacrylate] block copolymer (PtBA-hv-PDMAEMA, where -hv- is the photocleavable junction) into spherical micelles, followed by first PDMAEMA cross-linking by a bis-iodo compound and then by UV light irradiation. The exposure to light induces the cleavage of the junction between the PtBA core and the cross-linked PDMAEMA shell of the micelles. The PtBA block is then extracted to obtain the desired nanocages. The size change of the nanocages in response to pH and temperature is investigated by dynamic light scattering. Finally, the ability to functionalize the internal cavity of the nanocages is demonstrated.

Synthesis of photocleavable poly(methyl methacrylate-block-d -lactide) via atom-transfer radical polymerization and ring-opening polymerization

The synthesis and characterization of a photocleavable block copolymer containing an ortho-nitrobenzyl (ONB) linker between poly(methyl methacrylate) and poly(d-lactide) blocks is presented here. The block copolymers were synthesized via atom transfer radical polymerization (ATRP) of MMA followed by ring-opening polymerization (ROP) of d-Lactide and ROP of d-lactide followed by ATRP of MMA from a difunctional photoresponsive ONB initiator, respectively. The challenges and limitations during synthesis of the photocleavable block copolymers using the difunctional photoresponsive ONB initiator are discussed. The photocleavage of the copolymers occurs under mild conditions by simple irradiation with 302 nm wavelength UV light (Relative intensity at 7.6 cm: 1500 μW/cm2) for several hours. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4309–4316

Dynamic Substrate Based on Photocleavable Poly(ethylene glycol): Zeta Potential Determines the Capability of Geometrical Cell Confinement

Dynamic substrates whose cell adhesiveness changes in response to an external stimulus are useful not only for patterning cells in various geometries but also for inducing cell migration or arraying heterotypic cells. The requirements for such applications are high switching efficiency in cell adhesiveness and long-term persistence of the created cellular patterns. In this study, we prepared a dynamic substrate bearing photocleavable poly(ethylene glycol) (PEG) and examined the effect of the surface PEG density and the charge of cationic base materials on the above-mentioned key requirements. An amino-terminated substrate with a certain amino group density and charge was functionalized with photocleavable PEG5K, with and without subsequent backfilling of photocleavable PEG2K. The PEG chains made the surface non-cell-adhesive, but subsequent near-UV irradiation of the substrate induced photocleavage of the PEG, eventually making the surface cell-adhesive. The substrates were analyzed by atomic force microscopy, contact angle measurements, ellipsometry, and zeta potential measurements, complemented with protein adsorption observations. Although the density of amino group in the base material affected both the grafting efficiency of the backfilling PEG and the electrokinetic potential mainly in the positive range, the latter mainly determined the protein- and cell-repelling abilities of the substrates. Furthermore, varying the surface compositions had almost no effect on the switching efficiency in the early stage of the culture, but it became more significant after culturing cells for a longer time; the cells fouled the nonirradiated PEGylated regions earlier on the surfaces with higher positive zeta potentials. These results indicate that the zeta potential is an essential factor in the long-term persistence of cellular patterns on photoactivatable substrates. This study not only provides a recipe for the development of a dynamic substrate with an adequate time frame but also clarifies how the interfacial nanoarchitectures, composed of the nanometer-scale PEG brushes and charged base materials, affect the biocompatibility.

Multiresponsive Micellar Systems from Photocleavable Block Copolymers.

This contribution describes the synthesis and associating behavior in water of a multiresponsive amphiphilic diblock copolymer. This copolymer is composed of an hydrophobic photocleavable poly(para-methoxyphenacyl methacrylate) block (PMPMA) and a hydrophilic thermosensitive poly[(oligo ethylene glycol)methacrylate] block (POEGMA). The PMPMA-b-POEGMA copolymer forms micelles with a PMPMA core and a POEGMA corona in water. Light irradiation leads to the transformation of PMPMA into poly(methacrylic acid) (PMAA) and to the disruption of the initial micelles. The response of the accordingly obtained PMAA-b-POEGMA copolymer to pH, temperature, calcium (Ca2+), and phosphate (PO43-) ions is demonstrated.

Dynamic culture substrate that captures a specific extracellular matrix protein in response to light

The development of methods for the off–on switching of immobilization or presentation of cell-adhesive peptides and proteins during cell culture is important because such surfaces are useful for the analysis of the dynamic processes of cell adhesion and migration. This paper describes a chemically functionalized gold substrate that captures a genetically tagged extracellular matrix protein in response to light. The substrate was composed of mixed self-assembled monolayers (SAMs) of three disulfide compounds containing (i) a photocleavable poly(ethylene glycol) (PEG), (ii) nitrilotriacetic acid (NTA) and (iii) hepta(ethylene glycol) (EG7). Although the NTA group has an intrinsic high affinity for oligohistidine tag (His-tag) sequences in its Ni2+-ion complex, the interaction was suppressed by the steric hindrance of coexisting PEG on the substrate surface. Upon photoirradiation of the substrate to release the PEG chain from the surface, this interaction became possible and hence the protein was captured at the irradiated regions, while keeping the non-specific adsorption of non-His-tagged proteins blocked by the EG7 underbrush. In this way, we selectively immobilized a His-tagged fibronectin fragment (FNIII7–10) to the irradiated regions. In contrast, when bovine serum albumin—a major serum protein—was added as a non-His-tagged protein, the surface did not permit its capture, with or without irradiation. In agreement with these results, cells were selectively attached to the irradiated patterns only when a His-tagged FNIII7-10 was added to the medium. These results indicate that the present method is useful for studying the cellular behavior on the specific extracellular matrix protein in cell-culturing environments.

Photo-induced micellization of block copolymers bearing 4,5-dimethoxy-2-nitrobenzyl side groups

The synthesis of photocleavable poly(dimethoxynitrobenzyl acrylate)-block-polystyrene block copolymers is described. The UV irradiation of these block copolymers, dissolved in a good solvent for both blocks, selectively cleaves the dimethoxynitrobenzyl protecting groups, leading to carboxylic acid moieties. Since the resulting hydrophilic poly(acrylic acid) block is insoluble in the solvent used, self-assembly of the diblocks into micelles is observed. This light-induced micellization process is further used to trap dyes into the core of the micelles.

Environment-Friendly Photolithography Using Poly(N-isopropylacrylamide)-Based Thermoresponsive Photoresists

We report a novel approach for the temperature-triggered development of water-soluble photoresists based on photocleavable poly(N-isopropylacrylamide) copolymers. These copolymers are soluble in an aqueous environment below their Lower Critical Solution Temperature (LCST). Upon UV irradiation, the photocleavable groups are deprotected resulting in an increased LCST. Thus, the illuminated parts of spin-coated copolymer layers dissolve at higher temperatures than the surrounding areas, leading to pattern development. The photoresist can finally be completely removed at low temperature. We demonstrate the applicability of this novel photolithographic approach by the patterning of fluorescent proteins.

Synthesis of Photocleavable Poly(styrene-block-ethylene oxide) and Its Self-Assembly into Nanoporous Thin Films

Synthesis of Photocleavable Poly(styrene-<i>block</i>-ethylene oxide) and Its Self-Assembly into Nanoporous Thin Films

Grafting Poly(ethylene glycol) to a Glass Surface via a Photocleavable Linker for Light-induced Cell Micropatterning and Cell Proliferation Control

Abstract This paper describes a glass substrate having a photocleavable poly(ethylene glycol) (PEG) designed for light-induced cell micropatterning. The substrate changed from non-cell-adhesive to cell-adhesive by the photocleavage of PEG. Cellular patterns maintained for more than 17 days, and they were able to be changed to control cell migration and proliferation at multi- and single-cell levels by irradiating their adjacent regions during cell cultivation.