When solvent breaks a protein: protein unfolding under shear

Proteins break under the action of different perturbations, the temperature, chemicals, mechanical forces. Fluid flow too, in special condition, unfolds a protein. In some biological processes, the fluid induced perturbation is even functional. That is the case of blood coagulation where the long chain of the von Willibrend factor unrolls and extends under the action of blood shear flow caused by a vessel injury. Other proteins, known as catch-bonds, use the tensile force to strength the binding with their substrate via a sort of allosteric conformational change. It is therefore intriguing to understand in which conditions a protein unfolds in shear flow, and the molecular mechanism of the process. We have dedicated a recent paper to this by exploiting the power of the lattice Boltzmann MD technique. Surf it here.

Solvent disorder and protein dynamical transition

Protein dynamical transition (PDT) indicates the sudden activation of protein fluctuations above a critical temperature, Td ~ 220-240 K. The phenomenon has attracted the attention of scientists along the years because the possible implications. First, it has been strongly related to the role of the solvent environment surrounding the protein, and namely its physical changes. It is not surprising that many concepts coined in the community of liquids were transposed to scratch insights on the problem. Secondly, this problem represented the door through which the community active in neutron scattering entered heavily in the discussion about protein dynamics and function. Yet today, numerous  interesting works focusing on the protein dynamical transition appear in top-notch magazines, see e.g. Weik and coworkers discussed the correlation among water translation and protein fluctuation across the PDT [here] while Hong and coworkers claim that the transition is an intrinsic feature of the dry protein energy landscape [here]. We are participating to the debate, as presented in the post dedicated to Lindemann criterion. To better understand the relationship among protein motion and solvent behaviour, we have recently developed a methodology that using data from particle based simulations, can fruitfully estimate the change in the water  hydrogen bond connectivity, in space, in time, and in temperature. We show the PDT correlates to the sudden increase in the configurational disorder of the water HB network enveloping the proteins. Our finding links, in the spirit of the Adam–Gibbs relationship, the diffusivity of protein atoms, as quantified by the hydrogen mean-square displacements, and the thermodynamic solvent configurational entropy. Enjoy the paper here, and a comment in the P. Ball's blog Water in Biology.