Shubin Li’s research while affiliated with Harbin Institute of Technology and other places

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Publications (8)


Bovine serum albumin-based hydrogels: Preparation, properties and biological applications
  • Article

October 2024

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30 Reads

Chemical Engineering Journal

Changxin Shi

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Shubin Li

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Chao Li

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[...]

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Sucrose release property of pH-responsive artificial cells
a Schematic diagram showing the fluid and gel phase of pH-responsive molecules against solution pH. b Photos of the fluid phase (pH 10) and gel phase (pH 5). c Schematic illustration showing the responsive property of species A. d Motion trajectories of red fluorescent polystyrene microspheres at pH 7 (left image) and pH 6 (right image). Scale bar is 5 μm. e Oscillation of the inner solution diffusion coefficient of pH-responsive artificial cells as a function of time by alternating the solution pH between 6.5 and 6.6. f Sucrose leakage from pH-responsive artificial cells 20 min after melittin was added as a function of solution pH. The release concentration of sucrose is obtained from three independent samples. Data are presented as the mean values ± SDs, n = 3. Source data are provided as a Source Data file.
Construction of a two-species community of pH-responsive artificial cells (containing sucrose) (species A) and S. cerevisiae (species B) and its pH oscillatory environment
a Schematic illustration of solution pH oscillation caused by feedback between species A and B. b A typical solution pH oscillation of a two-species-community system as a function of time. Species A and B were 2.76 × 10⁶/mL and 4.36 × 10⁶/mL, respectively. c pH value of CO2 oversaturated (phase I, red curve) and saturated (phase II, blue curve) gadobutrol solution as a function of time. CO2 was injected into gadobutrol solution in phase I. The gadobutrol solution was saturated by CO2 from air in phase II. d The initial sucrose concentration and sucrose concentration at the end of oscillation after 960 min. The sucrose concentrations were obtained by adding 10% Triton X-100 into the solution to release sucrose from species A. The concentration of sucrose at initial and end (960 min) of oscillation was tested with three independent samples. Data are presented as the mean values ± SDs, n = 3. e Flow cytometry scatter plots of live-dead stained species B at the longest oscillation time (960 min). Live S. cerevisiae (species B) was stained with FDA (green, in Q3), and dead S. cerevisiae was stained with PI (red, in Q1). The total number of particles counted was 10,000. Source data are provided as a Source Data file.
Three-species community containing sucrose and G6P containing pH-responsive artificial cells (species A′), S. cerevisiae (species B) and NAD⁺ and G6PDH containing artificial cells (species C)
a Schematic diagram showing solution pH oscillation and NADH generation inside species C caused by the feedback between species A′ and species B. b A typical solution pH oscillation of a three-species-community system as a function of time with species A′ (6.10 × 10⁶/mL) containing 150 mM sucrose and 10 mM G6P, species B (4.36 × 10⁶/mL), and species C (4.36 × 10⁶/mL) containing 10 mM NAD⁺ and 10 μg/mL G6PDH. c Fluorescence intensity of the same community as (b) as a function of time. d Corresponding microscopy images of the community system at the time points in (b). The first column images were observed using a green filter for viewing species A′. The second column images were observed in bright field for viewing species B. The third column images were recorded using a blue filter for viewing species C. The fourth column images were the merged images of Columns 1, 2 and 3 of each row. Scale bar is 5 μm. e The fluorescence intensity of the same three-species communities as a function of time with the absence of G6PDH in species C (blue curve), G6P in species A′ (red curve), or NAD⁺ in species C (black curve). G6PDH and G6P are the abbreviations of glucose-6-phosphate dehydrogenase and glucose-6-phosphate, respectively. NAD⁺ and NADH are the abbreviations of nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide plus hydrogen. Source data are provided as a Source Data file.
Communication among spatially coded three-species communities
a The pH oscillation curve of community CA′B as a function of time. b The corresponding laser scanning confocal microscopy images at points 1, 2, and 3 in (a). c The fluorescence intensity of species C of community CA′B as a function of time. d The pH oscillation curve of CBA′ as a function of time. e The corresponding laser scanning confocal microscopy images at points 1, 2, and 3 in (d). f The fluorescence intensity of species C of community CBA′ as a function of time. g The pH oscillation curve of A′CB as a function of time. h The corresponding laser scanning confocal microscopy images at points 1, 2, and 3 in (g). i The fluorescence intensity of species C of community A′CB as a function of time. The mean fluorescence intensities of species C in (c), (f), and (i) are from ten independent samples. Data are presented as the mean values ± SDs, n = 10. G6P is the abbreviations of glucose-6-phosphate. Source data are provided as a Source Data file.
Regulation of species metabolism in synthetic community systems by environmental pH oscillations
  • Article
  • Full-text available

November 2023

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101 Reads

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5 Citations

Constructing a synthetic community system helps scientist understand the complex interactions among species in a community and its environment. Herein, a two-species community is constructed with species A (artificial cells encapsulating pH-responsive molecules and sucrose) and species B (Saccharomyces cerevisiae), which causes the environment to exhibit pH oscillation behaviour due to the generation and dissipation of CO2. In addition, a three-species community is constructed with species A′ (artificial cells containing sucrose and G6P), species B, and species C (artificial cells containing NAD⁺ and G6PDH). The solution pH oscillation regulates the periodical release of G6P from species A′; G6P then enters species C to promote the metabolic reaction that converts NAD⁺ to NADH. The location of species A′ and B determines the metabolism behaviour in species C in the spatially coded three-species communities with CA′B, CBA′, and A′CB patterns. The proposed synthetic community system provides a foundation to construct a more complicated microecosystem.

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Schematic illustration of light harvesting and metabolism mimicry artificial system. a) Scheme of cyanobacteria containing artificial cell for endosymbiosis mimicking. b) Chemical reaction equations involved in metabolism mimicking pathways.
Encapsulation of cyanobacteria inside GUVs. a) Encapsulation efficiency as a function of cyanobacteria concentration. The encapsulation efficiency was 3.4 ± 1.4%, 4.9 ± 1.7%, 6.1 ± 2.2%, 9.6 ± 3.8%, 11.9 ± 4.3%, 16.5 ± 0.6%, 27.1 ± 2.8%, 40.5 ± 12.2%, and 41.9 ± 14.2% with the cyanobacteria concentration of 7.7, 15.3, 22.9, 30.6, 38.3, 76.5 153.1, 229.5, and 306.1 mg mL⁻¹, respectively. Data are presented as mean values ± SD. b) The fraction of artificial cells containing less than five cyanobacteria and more than five cyanobacteria at different cyanobacteria concentrations. The fraction of artificial cells containing less than five cyanobacteria was 100%, 100%, 99.1%, 97.9%, 88.5%, 67.5%, 58.3%, 55.5%, and 55% with the cyanobacteria concentration of 7.7, 15.3, 22.9, 30.6, 38.3, 75.6, 153.1, 229.5, and 306.1 mg mL⁻¹, respectively. At least 100 vesicles were counted to obtain each data. Representative fluorescence microscopy images of the artificial cells containing a single c) and multiple d) cyanobacteria. e) The confocal image of the artificial cell containing one cyanobacterium with two cross‐section images. All scale bars were 20 µm. The artificial cells were labelled with NBD‐PE in the lipid bilayer (green fluorescence).
Chemical communications between cyanobacteria and “cytoplasm” inside the artificial cells. The representative images of artificial cells containing cyanobacteria, GOx, and HRP before (a) and after (b) the introduction of Amplex red and 24 h light illumination. The scale bars were 20 µm. c) The amount of produced glucose as a function of illumination time in the test tube. The colored bands indicate mean ± SD of three independent experiments. d) The corresponding scheme of cascade reactions between the cyanobacteria and “cytoplasm” inside an artificial cell. e) Fluorescence intensity of produced resorufin inside the artificial cells (containing both GOx and HRP, GOx and HRP only) against time. The colored bands indicate mean ± SD. At least 100 vesicles were counted to obtain each data. f) Chemical reaction equations involved in artificial cells.
Chemical communications between cyanobacteria and protoorganelle inside the artificial cells. The representative images of artificial cells containing cyanobacteria, GOx, and protoorganelle (containing HRP) before (a) and after (b) 24 h light illumination with the introduction of Amplex red. c) The corresponding scheme of cascade reactions between the cyanobacteria and protoorganelle inside an artificial cell. d) Fluorescence intensity of produced resorufin in the prtotoorganelle (red curve) and “cytosol” (green curve) with HRP inside protoorganelle and GOx in the “cytosol”. e) The control experiments with GOx in the “cytosol”, but with no HRP inside protoorganelle. f) The control experiments with HRP inside protoorganelle, but with no GOx in the “cytosol”. The coloured bands indicate mean ± SD. At least 30 vesicles were counted to obtain each data. The scale bars were 20 µm.
The cascade cycling of NADH/NAD⁺ inside cyanobacteria‐containing artificial cells. a) The scheme of NADH production inside an artificial cell. b) Fluorescence microscope image of a cyanobacteria‐containing artificial cell after 24 h continuous daylight lamp illumination. Green, blue, and red fluorescence represent phospholipid membrane, NADH and the cyanobacteria, respectively. c) The normalized λem (460 nm) intensity (%) versus time curves in the artificial cells. The colored bands indicate mean ± SD of independent experiments (n = 3). d) The scheme of lactate production inside an artificial cell. e) The fluorescence microscope images of artificial cells (with and without pyruvate (73.1 × 10‐6 m)) and plot of blue fluorescence intensities across artificial cells with and without pyruvate (73.1 × 10‐6 m), respectively. f) The relative fluorescence intensities at different pyruvate concentrations (0, 36.5, 73.1 × 10‐6 m) in artificial cells (containing cyanobacteria, NAD⁺, GDH, LDH) after heating at 45°C for 2 h. Statistical analyses were carried out by two‐tailed unpaired student's t‐test (**p < 0.01). p < 0.05 was considered statistically significant. The error bars were the standard deviation. At least 100 vesicles were counted to obtain each data. g) Chemical reaction equations involved in the artificial cells. The scale bars were 20 µm.
Light‐Harvesting Artificial Cells Containing Cyanobacteria for CO2 Fixation and Further Metabolism Mimicking

July 2022

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65 Reads

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16 Citations

The bottom‐up constructed artificial cells help to understand the cell working mechanism and provide the evolution clues for organisms. The energy supply and metabolism mimicry are the key issues in the field of artificial cells. Herein, an artificial cell containing cyanobacteria capable of light harvesting and carbon dioxide fixation is demonstrated to produce glucose molecules by converting light energy into chemical energy. Two downstream “metabolic” pathways starting from glucose molecules are investigated. One involves enzyme cascade reaction to produce H2O2 (assisted by glucose oxidase) first, followed by converting Amplex red to resorufin (assisted by horseradish peroxidase). The other pathway is more biologically relevant. Glucose molecules are dehydrogenated to transfer hydrogens to nicotinamide adenine dinucleotide (NAD⁺) for the production of nicotinamide adenine dinucleotide hydride (NADH) molecules in the presence of glucose dehydrogenase. Further, NADH molecules are oxidized into NAD⁺ by pyruvate catalyzed by lactate dehydrogenase, meanwhile, lactate is obtained. Therefore, the cascade cycling of NADH/NAD⁺ is built. The artificial cells built here pave the way for investigating more complicated energy‐supplied metabolism inside artificial cells.


An artificial cell containing cyanobacteria for endosymbiosis mimicking

April 2021

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77 Reads

The bottom-up constructed artificial cells help to understand the cell working mechanism and provide the evolution clues for organisms. Cyanobacteria are believed to be the ancestors of chloroplasts according to endosymbiosis theory. Herein we demonstrate an artificial cell containing cyanobacteria to mimic endosymbiosis phenomenon. The cyanobacteria sustainably produce glucose molecules by converting light energy into chemical energy. Two downstream "metabolic" pathways starting from glucose molecules are investigated. One involves enzyme cascade reaction to produce H2O2 (assisted by glucose oxidase) first, followed by converting Amplex red to resorufin (assisted by horseradish peroxidase). The more biological one involves nicotinamide adenine dinucleotide (NADH) production in the presence of NAD+ and glucose dehydrogenase. Further, NADH molecules are oxidized into NAD+ by pyruvate catalyzed by lactate dehydrogenase, meanwhile, lactate is obtained. Therefore, the sustainable cascade cycling of NADH/NAD+ is built. The artificial cells built here simulate the endosymbiosis phenomenon, meanwhile pave the way for investigating more complicated sustainable energy supplied metabolism inside artificial cells.


Fig. 1 Assembly of giant unilamellar vesicles (GUVs) on stainless steel (SS) mesh under vertical magnetic field. a Schematic illustration of the device for GUVs assembly: a SS mesh placed on the top center of a magnet. b Horizontal (top) and vertical (bottom) central section of the simulated magnetic field distribution across the microwells. The white dash box and the black dash circle respectively indicated the unit of the microwell array and the approximating unit for decentralized microwells. The black dash arrow indicated the preferential localization of GUVs around microwell wall. c Fluorescence images of the GUVs colonies with different extent of occupation of the microwells. The white dash circle indicated microwell wall. d Fluorescence image of GUV colony arrays formed in SS mesh with microwell diameter of 250 μm. e Top view and side view along the yellow dash section line of the GUVs colony taken by a laser confocal microscope. f A 3D image of GUVs colony obtained from serial sections of images in the Z-stacks taken by a laser confocal microscope. g Fluorescence images of GUVs colonies with different morphologies: from left to right, triangular, square, striped, and HITlike assemblies. The dash triangle, rectangle, and line illustrated rough outline of GUVs colonies. h The schematic and simulated magnetic field distribution of SS mesh with densely packed microwells. The white dash box presented the unit of the microwell array. The black arrows indicated the corners. i Fluorescence images of the Chinese ancient coin-like round GUVs colonies with square holes formed using the SS mesh with densely packed microwells. The bottom is the enlarged image in the dash box of top image as indicated by the yellow dash arrow. The white dash box in bottom image indicated the square hole in GUVs colony. The scale bars are 100 μm.
Assembly of GUVs on the SS mesh under horizontal and inclined magnetic field
a The schematic of the device for horizontal magnetic field. b Simulated magnetic field distribution on the top surface of the SS mesh under horizontal magnetic field. c Fluorescence images of the GUVs colonies formed under horizontal magnetic field. The right image is the enlarged image in the yellow dash box of the left image. d The schematic of the device for inclined magnetic field (with directions between the vertical and horizontal magnetic fields) by putting the SS mesh on one side of the top of the magnet. e Simulated magnetic field distribution at the bottom surface of the SS mesh under inclined magnetic field. f Fluorescence images of the GUVs colonies under inclined magnetic field. The right image is the enlarged image in the yellow dash box of the left image. The dash circles in b, c, e, and f indicate the microwells. The scale bars in c and f are 200 μm.
Coding of spatially controlled GUVs colonies
a Schematic and fluorescence images of GUVs colonies formed via the parallel coding of giant unilamellar vesicles with green fluorescence (gGUVs) and giant unilamellar vesicles with red fluorescence (rGUVs). Schematic and fluorescence images of the serially coded GUVs colonies via application of vertical magnetic field for the alternative assembly of gGUVs and rGUVs (b), successive application of two inclined magnetic fields with different directions respectively for gGUVs assembly (putting the SS mesh on one side of the magnet) and rGUVs (putting the SS mesh on the other side of the magnet) (c), successive application of inclined magnetic field for gGUVs assembly and vertical magnetic field for rGUVs assembly (d), successive application of two perpendicular horizontal magnetic fields for the chronological assembly of gGUVs and rGUVs (e), and successive application of vertical magnetic field for gGUVs assembly and two perpendicular horizontal magnetic fields for rGUVs assembly (f). The dash circles indicated the microwell wall. The scale bars are 100 μm.
Spatialized biochemical reactions in tissue-like GUVs aggregates
a Schematic illustration for the chemical communication between the colony of gGUVs with melittin and the non-labeled GUVs colony. b Fluorescence image and bright field image of the GUVs aggregates with two coaxial GUVs colonies: fluorescence image of the colonies of gGUVs with melittin (left), bright field image of the two kind of colonies (middle), merged image (right). c Fluorescence images of the GUVs aggregates against time after the biochemical reaction was initiated by the addition of glucose and Amplex Red. d Variation of the fluorescence intensity of the product against time. The error bar represents the standard error of mean (SEM), n = 3 independent experiments. e Fluorescence images of the tissue-like GUVs aggregates with fluorescent resorufin product: fluorescent image of gGUVs colony (left), fluorescent image of the product of resorufin (middle), merged image (right). f Schematic illustration of the cell death caused by H2O2 that is generated by the GUVs colonies. g Images for the H2O2 caused cell death: bright field image of GUVs colonies and cell colonies (the first one), fluorescence image of live cells (the second one), fluorescence image of dead cells (the third one), and merged image (the last one). GOD in a and f represents glucose oxidase. HRP in a represents horseradish peroxidase. The scale bars were 100 μm. Source data are provided as a Source Data file.
Programmed magnetic manipulation of vesicles into spatially coded prototissue architectures arrays

January 2020

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380 Reads

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85 Citations

In nature, cells self-assemble into spatially coded tissular configurations to execute higher-order biological functions as a collective. This mechanism has stimulated the recent trend in synthetic biology to construct tissue-like assemblies from protocell entities, with the aim to understand the evolution mechanism of multicellular mechanisms, create smart materials or devices, and engineer tissue-like biomedical implant. However, the formation of spatially coded and communicating micro-architectures from large quantity of protocell entities, especially for lipid vesicle-based systems that mostly resemble cells, is still challenging. Herein, we magnetically assemble giant unilamellar vesicles (GUVs) or cells into various microstructures with spatially coded configurations and spatialized cascade biochemical reactions using a stainless steel mesh. GUVs in these tissue-like aggregates exhibit uncustomary osmotic stability that cannot be achieved by individual GUVs suspensions. This work provides a versatile and cost-effective strategy to form robust tissue-mimics and indicates a possible superiority of protocell colonies to individual protocells. To execute higher-order functions, cells self-assemble into spatially coded tissue configurations. Here the authors magnetically assembly giant unilamellar vesicles into three dimensional tissue-mimic structures with collective osmotic stability.


The morphology control of ghost. (a) The image of RBC. (b) DiO labeled isotonic ghosts. (c) Diameter statistics of isotonic ghost. (d‐f) Ghost in 75 mOsm, 90 mOsm,120 mOsm PBS. (g) Thickness statistics of ghosts in 75 mOsm, 90 mOsm, 120 mOsm PBS. (h) Proteinase K treated ghosts in 150 mOsm PBS. (i) Diameter statistics of proteinase K treated ghosts before and after hypertonic condition.
Electroless plating of the spherical microshells, and the formation of bowl‐like microshells. (a‐c) Microscope and SEM images of spherical hollow microshells, and diameters statistics. (d‐f) Microscope and SEM images of bowl‐like microshells, and notches diameters statistics.
Bubbles driven movement of Janus bowl‐like micromotors in H2O2. (a‐b) Frame rate sequence images and trajectory fitting of the bowl‐like micromotor in 5% H2O2. (c) Average velocity in different concentrations of H2O2 solution.
Schematic illustration of the preparation and self‐propelled movement of bowl‐like micromotor.
Bowl‐like Micromotors Using Red Blood Cell Membrane as Template

September 2019

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180 Reads

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9 Citations

The asymmetric micro/nano motors have attracted great attentions recently, because they convert external physical and chemical energy into the kinetic energy. Red blood cell (RBC) membranes with good deformability and fluidity are excellent natural templates for micromaterial fabrication. Herein, RBC membranes were used as templates to prepare bowl‐like micro‐motors by electroless plating platinum particle onto the membranes. The asymmetric Pt bowl‐like micromotors were driven by hydrogen peroxide.


Chemical Signal Communication between Two Protoorganelles in a Lipid Based Artificial Cell

April 2019

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47 Reads

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56 Citations

Analytical Chemistry

The chemical signal communication among organelles in the cell is extremely important for life. We hereby demonstrated that the chemical signal communication between two protoorganelles using cascade enzyme reactions in a lipid based artificial cell. Two protoorganelles inside the artificial cell are the large unilamellar vesicles containing glucose oxidase (GOx-LUVs) and the vesicle containing (horseradish peroxidase (HRP) and Amplex red), respectively. The glucose molecules outside the artificial cell penetrate the lipid bilayer through mellitin pores and enter into one protoroganelle (GOx-LUVs) to produce H2O2, which subsequently transport to the other protoorganelle to oxidize Amplex red into red resorufin catalyzed by HRP. The number of GOx-LUVs in an artificial cell is controlled by using GOx-LUVs solution with different density during the electroformation. The reaction rate for resorufin in the protoorganelle increases with more GOx-LUVs inside the artificial cell. The artificial cell developed here paves the way for more complicated signal transduction mechanism study in a eukaryocyte.


A green method to synthesize flowerlike Fe(OH) 3 microspheres for enhanced adsorption performance toward organic and heavy metal pollutants

February 2018

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45 Reads

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63 Citations

Journal of Environmental Sciences

Dyestuffs and heavy metal ions in water are seriously harmful to the ecological environment and human health. Three-dimensional (3D) flowerlike Fe(OH)3 microspheres were synthesized through a green yet low-cost injection method, for the removal of organic dyes and heavy metal ions. The Fe(OH)3 microspheres were characterized by thermal gravimetric analysis (TGA), Fourier transform infrared (FT-IR), and transmission electron microscopy (TEM) techniques. The adsorption kinetics of Congo Red (CR) on Fe(OH)3 microspheres obeyed the pseudo-second-order model. Cr⁶⁺ and Pb²⁺ adsorption behaviors on Fe(OH)3 microspheres followed the Langmuir isotherm model. The maximum adsorption capacities of the synthesized Fe(OH)3 were 308, 52.94, and 75.64mg/g for CR, Cr⁶⁺, and Pb²⁺ respectively. The enhanced adsorption performance originated from its surface properties and large specific surface area of 250m²/g. The microspheres also have excellent adsorption stability and recyclability. Another merit of the Fe(OH)3 material is that it also acts as a Fenton-like catalyst. These twin functionalities (both as adsorbent and Fenton-like catalyst) give the synthesized Fe(OH)3 microspheres great potential in the field of water treatment.

Citations (6)


... In such systems, supramolecular structures form and change in a pre-programmed manner, controlled by external stimuli such as chemical or light triggers, and typically result in changes in molecular structure [10][11][12] . These transient and dynamic systems have been investigated in the bulk, as well as within droplets 13,14 . The processes occurring in these systems are often comparable or analogous to those found within cells, especially when confined within droplets. ...

Reference:

Forging out-of-equilibrium supramolecular gels
Regulation of species metabolism in synthetic community systems by environmental pH oscillations

... As a readout, we used the protein Hyper7, a hydrogen peroxide responsive fluorescent protein 54 . To generate hydrogen peroxide we used glucose oxidase [55][56][57] . One population of GUVs, marked with pre-expressed mCherry, expresses αHL with the K3 loop insert and also contains glucose oxidase (sender cells). ...

Light‐Harvesting Artificial Cells Containing Cyanobacteria for CO2 Fixation and Further Metabolism Mimicking

... [1][2][3][4] Due to their ability to mimic these key characteristics of cells, GUVs show promise for applications in soft matter, 5-8 biomedicine, [9][10][11] and bottom-up synthetic biology. [12][13][14] GUVs are routinely obtained using thin film hydration, which are a class of methods that involves hydrating dry thin lipid films with low ionic strength aqueous solutions. [15][16][17][18] We recently reported an analytical framework to quantify the distribution of diameters and molar yields of populations of GUVs using sedimentation, high-resolution confocal microscopy, and large data set image analysis. ...

Programmed magnetic manipulation of vesicles into spatially coded prototissue architectures arrays

... Shape can dictate propulsion by, for example, trapping the catalyst in a cavity with only one opening, forcing the propelling force through this one outlet [14][15][16][17]. Other methods of dictating the location of propulsion force are through concave shapes [6,18], as oversaturation is more easily reached there, or by differences in surface roughness, since roughness enables bubble pinning and can thus enhance the speed of bubble propelled motors [3,7]. Asymmetry in catalyst distribution directly dictates the location of the propulsion force, since the location of the catalyst is where the reaction happens and, thus, where the propelling products are formed. ...

Bowl‐like Micromotors Using Red Blood Cell Membrane as Template

... As a readout, we used the protein Hyper7, a hydrogen peroxide responsive fluorescent protein 54 . To generate hydrogen peroxide we used glucose oxidase [55][56][57] . One population of GUVs, marked with pre-expressed mCherry, expresses αHL with the K3 loop insert and also contains glucose oxidase (sender cells). ...

Chemical Signal Communication between Two Protoorganelles in a Lipid Based Artificial Cell
  • Citing Article
  • April 2019

Analytical Chemistry

... The nanocomposites has two different lattice distances, 0.256 nm and 0.246 nm, as seen by the HRTEM pictures in figure 2(d), respectively. Among them, Ti 3 C 2 T x 's (100) crystal face is located at 0.256 nm, and the standard card of iron hydroxide substance is 0.246 nm [49]. Figure 2(e) represents the EDS composition diagram of the 7.7 wt% Fe(OH) 3 /Ti 3 C 2 T x nanocomposites, which indicates the arrangement of C, O, Ti, and Fe elements, respectively. ...

A green method to synthesize flowerlike Fe(OH) 3 microspheres for enhanced adsorption performance toward organic and heavy metal pollutants
  • Citing Article
  • February 2018

Journal of Environmental Sciences