Difference between revisions of "Pair Potential of Charged Colloidal Stars."

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[[Image:M13-Polystyrene-Star(TEM Fluorescence).JPG|thumb|right|300px|TEM (left) and fluorescence microscopy (right) images of M13 virus - polystyrene bead colloidal stars of different grafting intensities: c) 3 phages/bead, d) 38 phages/bead, e) 135 phages/bead.  Brighter fluorescence indicates higher virus density.]]
 
==Keywords==
 
==Keywords==
[[Pair Interaction]], [[M13 Virus]], [[Polymer_molecules#Polystyrene_.E2.80.93_Plastic_cups_and_Styrofoam|Polystyrene]]
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====Biotinylation, [[M13 Virus]], Pair Interaction Potential, Phage Display, Polymer Star, [[Polymer_molecules#Polystyrene_.E2.80.93_Plastic_cups_and_Styrofoam|Polystyrene]]====
  
 
==Summary==
 
==Summary==
This paper describes the construction of "colloidal stars", polystyrene polymer spheres with M13 bacteriophage grafted onto their surface.  Polystyrene is the same material that is used in plastic cups and styrofoam (styrofoam is foamed polystyrene).  The beads were 1<math>\mu</math>m in diameter, while the cylindrical M13 viruses where 880nm in length and 6.6nm in diameter.  They had a persistence length of 2<math>\mu</math>m, making them semiflexible, unlike flexible DNA polymer stars made previously by other groups.  The M13 viruses attached to the polymer spheres on their ends,  
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This paper describes the construction of "colloidal stars", polystyrene polymer spheres with M13 bacteriophage grafted onto their surface.  Polystyrene is the same material that is used in plastic cups and styrofoam (styrofoam is foamed polystyrene).  The beads were 1<math>\mu</math>m in diameter, while the cylindrical M13 viruses were 880nm in length and 6.6nm in diameter.  They had a persistence length of 2<math>\mu</math>m, making them semiflexible, unlike flexible DNA polymer stars made previously by other groups.  Additionally, the viruses held a linear charge density of ~7 electrons/nm.  The M13 viruses attached to the polymer spheres on their ends, using biotinylation.  Biotinylation refers to the process of tagging a substance, in this case the M13 virus, with biotin (also know as Vitamin H or B7).  Biotin has a strong affinity for another molecule, streptavidin, so a common technique is to bind biotin to one substance and streptavidin to another in order to make them contact.  The authors coated the polystyrene beads with streptavidin, which is why the M13 viruses bound to the beads.  In biotinylation, the authors also made use of a phage display.  The fundamental concept of a phage display is that by genetically engineering the DNA inside a virus like M13 we can alter the proteins present on its protein capsid.  Different protein sequences (peptides) have different chemical affinities for various substances, so by trying out a large range of different peptide sequences, we can pick out the ones with the highest affinity for the material of interest.  In addition, the authors labeled the viruses using fluorescent dye molecules, allowing them to use fluorescence imaging to correlate intensity of fluorescence with how many viruses are bound to the polystyrene beads.  As expected, they found that increasing the ratio of biotinylated M13 viruses to steptavidin-bound polystyrene beads corresponded to a higher density of viruses on the beads.  The paper goes on to present characterization of the polymer stars, including their pair interaction potentials, which pretty closely match predicted theoretical values.
  
 
==Relevance for Soft Matter==
 
==Relevance for Soft Matter==
 +
The main draw for this kind of research is the discovery and invention of new colloidal materials.  In this paper, the authors were able to genetically engineer viruses to attach to polymer beads; many variables are controllable, including the composition of the virus coat and length (through genetic engineering), grafting density of viruses (through stoichiometric ratio of biotinylated viruses to streptavidin-bound polymer beads), diameter of beads (they also were able to produce 10nm gold beads with viruses grafted on), etc.  The ability to make synthetic and hybrid colloids opens the door to studying interesting and new properties and observing colloids with more complex phases.  Moreover, access to these types of structures allows us to test and refine models describing the behavior of colloids, such as how to calculate excluded volume and pair potential functions. 
  
 
==References==
 
==References==
 
F. Huang, K. Addas, A. Ward, N.T. Flynn, E. Velasco, M.F. Hagan, Z. Dogic, and S. Fraden. "Pair Potential of Charged Colloidal Stars". ''Physical Review Letters'' 102, 108302 (2009).
 
F. Huang, K. Addas, A. Ward, N.T. Flynn, E. Velasco, M.F. Hagan, Z. Dogic, and S. Fraden. "Pair Potential of Charged Colloidal Stars". ''Physical Review Letters'' 102, 108302 (2009).
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 +
  
 
==Pair Potential of Charged Colloidal Stars (by Hsin-I Lu)==
 
==Pair Potential of Charged Colloidal Stars (by Hsin-I Lu)==

Latest revision as of 04:38, 23 November 2009

TEM (left) and fluorescence microscopy (right) images of M13 virus - polystyrene bead colloidal stars of different grafting intensities: c) 3 phages/bead, d) 38 phages/bead, e) 135 phages/bead. Brighter fluorescence indicates higher virus density.

Keywords

Biotinylation, M13 Virus, Pair Interaction Potential, Phage Display, Polymer Star, Polystyrene

Summary

This paper describes the construction of "colloidal stars", polystyrene polymer spheres with M13 bacteriophage grafted onto their surface. Polystyrene is the same material that is used in plastic cups and styrofoam (styrofoam is foamed polystyrene). The beads were 1<math>\mu</math>m in diameter, while the cylindrical M13 viruses were 880nm in length and 6.6nm in diameter. They had a persistence length of 2<math>\mu</math>m, making them semiflexible, unlike flexible DNA polymer stars made previously by other groups. Additionally, the viruses held a linear charge density of ~7 electrons/nm. The M13 viruses attached to the polymer spheres on their ends, using biotinylation. Biotinylation refers to the process of tagging a substance, in this case the M13 virus, with biotin (also know as Vitamin H or B7). Biotin has a strong affinity for another molecule, streptavidin, so a common technique is to bind biotin to one substance and streptavidin to another in order to make them contact. The authors coated the polystyrene beads with streptavidin, which is why the M13 viruses bound to the beads. In biotinylation, the authors also made use of a phage display. The fundamental concept of a phage display is that by genetically engineering the DNA inside a virus like M13 we can alter the proteins present on its protein capsid. Different protein sequences (peptides) have different chemical affinities for various substances, so by trying out a large range of different peptide sequences, we can pick out the ones with the highest affinity for the material of interest. In addition, the authors labeled the viruses using fluorescent dye molecules, allowing them to use fluorescence imaging to correlate intensity of fluorescence with how many viruses are bound to the polystyrene beads. As expected, they found that increasing the ratio of biotinylated M13 viruses to steptavidin-bound polystyrene beads corresponded to a higher density of viruses on the beads. The paper goes on to present characterization of the polymer stars, including their pair interaction potentials, which pretty closely match predicted theoretical values.

Relevance for Soft Matter

The main draw for this kind of research is the discovery and invention of new colloidal materials. In this paper, the authors were able to genetically engineer viruses to attach to polymer beads; many variables are controllable, including the composition of the virus coat and length (through genetic engineering), grafting density of viruses (through stoichiometric ratio of biotinylated viruses to streptavidin-bound polymer beads), diameter of beads (they also were able to produce 10nm gold beads with viruses grafted on), etc. The ability to make synthetic and hybrid colloids opens the door to studying interesting and new properties and observing colloids with more complex phases. Moreover, access to these types of structures allows us to test and refine models describing the behavior of colloids, such as how to calculate excluded volume and pair potential functions.

References

F. Huang, K. Addas, A. Ward, N.T. Flynn, E. Velasco, M.F. Hagan, Z. Dogic, and S. Fraden. "Pair Potential of Charged Colloidal Stars". Physical Review Letters 102, 108302 (2009).


Pair Potential of Charged Colloidal Stars (by Hsin-I Lu)

Summary

This paper reported the construction of colloidal stars: 1 <math>\mu</math>m polystyrene beads grafted with a dense brush of 1 <math>\mu</math>m long and 10 nm wide charged semiflexible filamentous viruses. The pair interaction potential of colloidal stars are studied under optical traps and measured using an implementation of umbrella sampling. The influence of ionic strength and grafting density on the interaction is measured and in good agreement with theoretical predictions.

Soft matter keywords

osmotic pressure, laser tweezers, colloid, TEM

Soft Matter

Colloidal stars.jpg
Fig.2
Fig. 3 (c), Symbols: experiment; dashed lines: theory; solid lines: single exponential fits. (<math>\circ</math>, x') and (x): 2.8 mM; (<math>\triangle</math>, y') and (y): 14 mM; (<math>\Box</math>, z') and (z): 28 mM.
  • Colloid stars:

Colloid stars are constructed by grafting M13 viruses to polystyrene spheres. The viruses are rodlike, semiflexible charged polymers of length <math>L=880</math> nm, diameter <math>D=6.6</math> nm, and persistence length ~ 2 <math>\mu</math>m with a linear charge density of ~<math>7 e^{-1}</math>/nm. The M13 are rigid enough to form liquid crystals, but when grafted to a sphere remain flexible enough to be distorted by the director field.

Fig.1 (a) and (b) show TEM images of 10 nm Au-bound M13 viruses of different nanoarchitectures and (c)–(e) show TEM (right panel) and fluorescence (left panel) images of labeled phage grafted to unlabeled 1<math>\mu</math>m PS beads with varying grafting densities. (c) 3 phages/bead. (d) 38 phages/bead. (e) 135 phages/bead. At the grafting density of 135 phages/bead [Fig. 1(e)], the anchored dye-labeled rods form a spherically symmetric corona around the bead.

  • Measurement of interaciton potential:

The potential of mean force as a function of separation between two colloidal particles <math>W_{int} (r)</math>can be determined up to an additive offset by the Boltzmann relation, <math>P(r) \sim exp(-W_{int} (r) /k_B T)</math>. Therefore, measuring the probability <math>P(r)</math> of finding the particles at a separation r can determine <math>W_{int} (r)</math>. Typically for states of even moderate repulsive interaction energies (few <math>k_B T</math>) <math>P(r)</math> becomes very small. Using optical field to displace colloidal stars in various distance, the authors can construct single interparticle pair-potentialcan from seperate measuremnts.

Fig. 2 shows two colloidal stars in separate laser traps and the histogram of separation distances between the colloids. Since there is repulsion interaction between stars, the seperation would be larger than two bare beads (Fig. 2(a)). In Fig. 2(c), separation histograms of bare beads (A) and phage-grafted beads (B) confirmed this point. To meausre the full range of <math>W_{int} (r)</math>, the authors measured <math>P(r)</math> for 30 different trap positions with 50 nm increments in separation. In each seperation the stars fluctuate about the minimum of a total potential resulting from a combination of the dual traps and interparticle star potential. Only 6kBT of each of the total potentials is sampled and each minimum has a different energy. The overlap between windows can be combined to produce a single interparticle pair-potential.

To extrapolate <math>W_{int} (r)</math> between to stars under the infulence of external optical field, the authors performed two experiments for any given trap seperation. In one experiment, two colloidal stars were placed in two separate laser traps and in the other experiment two bare colloids were placed in the same two traps. For both experiments, the separation histogram of the colloids was measured. The potential of mean force, <math>W_{sub}</math>, is then obtained by subtracting the results from each experiment.

<math>W_{sub}(r) /k_B T = -log(f_f(r)) + log(f_{nf} (r))</math>,

with <math>f_f(r)</math> and <math>f_{nf}(r)</math> the fraction of measured displacements that fall within the histogram bin associated with the displacement value <math>r</math> for functionalized and nonfunctionalized beads, respectively.

Fig. 3 (b) shows the interaction potentials of colloidal stars at varying solution ionic strengths with 135 phages/bead.

  • Discussion:

By attaching viruses to polystyrene spheres and trapping polystyrene spheres in optical fields, the interaction of colloidal stars due to repulsion between charged viruses can be measured. This technique can be used to studied the interactions between hybrid colloidal materials. As mentioned in the paper, this method allows measurement of strong repulsive potentials of the order of 100 <math>k_B T</math> given the laser power (which determines the optical trap depth) and optical resolution in the experiment.