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Theoretical physicists working at a blackboard collaboration pod in the Beecroft building.
Credit: Jack Hobhouse

Prof Ramin Golestanian

Professor of Theoretical Condensed Matter Physics

Sub department

  • Rudolf Peierls Centre for Theoretical Physics

Research groups

  • Condensed Matter Theory
Ramin.Golestanian@physics.ox.ac.uk
Telephone: 01865 273974
Rudolf Peierls Centre for Theoretical Physics, room 60.12
Max Planck Institute for Dynamics and Self-Organization
Oxford Podcast (2014): Living Matter & Theo Phys
Oxford Podcast (2017): The bacterial Viewpoint
  • About
  • Teaching
  • Publications

Counterions between charged polymers exhibit liquid-like organization and dynamics.

Proc Natl Acad Sci U S A 103:21 (2006) 7962-7967

Authors:

Thomas E Angelini, Ramin Golestanian, Robert H Coridan, John C Butler, Alexandre Beraud, Michael Krisch, Harald Sinn, Kenneth S Schweizer, Gerard CL Wong

Abstract:

Current understanding of electrostatics in water is based on mean-field theories like the Poisson-Boltzmann formalism and its approximations, which are routinely used in colloid science and computational biology. This approach, however, breaks down for highly charged systems, which exhibit counterintuitive phenomena such as overcharging and like-charge attraction. Models of counterion correlations have been proposed as possible explanations, but no experimental comparisons are available. Here, collective dynamics of counterions that mediate like-charge attraction between F-actin filaments have been directly observed in aqueous solution using high-resolution inelastic x-ray scattering down to molecular length-scales. We find a previously undescribed acoustic-like phonon mode associated with correlated counterions. The excitation spectra at high wave-vector Q reveal unexpected dynamics due to ions interacting with their "cages" of nearest neighbors. We examine this behavior in the context of intrinsic charge density variations on F-actin. The measured speed of sound and collective relaxation rates in this liquid agree surprisingly well with simple model calculations.
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Efficient in-depth trapping with an oil-immersion objective lens.

Opt Lett 31:6 (2006) 766-768

Authors:

S Nader S Reihani, Mohammad A Charsooghi, Hamid R Khalesifard, Ramin Golestanian

Abstract:

Maximum trapping efficiency in optical tweezers occurs close to the coverslip because spherical aberration owing to a mismatch in the refractive indices of the specimen (water) and the immersion oil dramatically decreases the trap efficiency as the trap depth increases. Measuring the axial trap efficiency at various tube lengths by use of an oil-immersion objective has shown that such an aberration can be balanced by another source of spherical aberration, leading to a shift in the position of the maximum efficiency in the Z direction. For a 1.1 microm polystyrene bead we could achieve the maximal efficiency at a depth of 70 microm, whereas the trap was stable up to a depth of 100 microm.
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Measuring lateral efficiency of optical traps: The effect of tube length

Optics Communications 259:1 (2006) 204-211

Authors:

SNS Reihani, HR Khalesifard, R Golestanian

Abstract:

An optical tweezer setup is made based on a custom-designed inverted microscope, which can work both in finite and infinite tube length microscopy modes. It is shown that the spherical aberration due to the mismatch in the refractive indices of the specimen (water) and the immersion oil as well as the wavelength can be partially compensated by introducing another source for the spherical aberration provided it has the opposite sign. Changing the tube length is shown to be a good candidate for this effect: an improvement of up to a factor of four has been observed in the lateral efficiency of the trap. © 2005 Elsevier B.V. All rights reserved.
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Condensation of DNA-actin polyelectrolyte mixtures driven by ions of different valences.

Phys Rev E Stat Nonlin Soft Matter Phys 73:3 Pt 1 (2006) 031911

Authors:

Olena V Zribi, Hee Kyung, Ramin Golestanian, Tanniemola B Liverpool, Gerard CL Wong

Abstract:

Multivalent ions can induce condensation of like-charged polyelectrolytes into compact states, a process that requires different ion valences for different polyelectrolyte species. In this work we examine the condensation behavior in binary anionic polyelectrolyte mixtures consisting of DNA coils and F-actin rods in the presence of monovalent, divalent, and trivalent ions. As expected, monovalent ions do not condense either component and divalent ions selectively condense F-actin rods out of the polyelectrolyte mixture. For trivalent ions, however, we observe a microphase separation between the two polyelectrolytes into coexisting finite-sized F-actin bundles and DNA toroids. Further, by increasing the DNA volume fraction in the mixture, condensed F-actin bundles can be completely destabilized, leading to only DNA condensation within the mixture. We examine a number of possible causes and propose a model based on polyelectrolyte competition for ions.
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Can nonlinear elasticity explain contact-line roughness at depinning?

Phys Rev Lett 96:1 (2006) 015702

Authors:

Pierre Le Doussal, Kay Jörg Wiese, Elie Raphael, Ramin Golestanian

Abstract:

We examine whether cubic nonlinearities, allowed by symmetry in the elastic energy of a contact line, may result in a different universality class at depinning. Standard linear elasticity predicts a roughness exponent zeta = 1/3 (one loop), zeta = 0.388 +/- 0.002 (numerics) while experiments give zeta approximately = 0.5. Within functional renormalization group methods we find that a nonlocal Kardar-Parisi-Zhang-type term is generated at depinning and grows under coarse graining. A fixed point with zeta approximately = 0.45 (one loop) is identified, showing that large enough cubic terms increase the roughness. This fixed point is unstable, revealing a rough strong-coupling phase. Experimental study of contact angles theta near pi/2, where cubic terms in the energy vanish, is suggested.
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