IR laser-induced perturbations of the voltage-dependent solute carrier protein SLC26a5

Biophys J. 2013 Oct 15;105(8):1822-8. doi: 10.1016/j.bpj.2013.09.008.

Abstract

Alterations in membrane capacitance can arise from linear and nonlinear sources. For example, changes in membrane surface area or dielectric properties can modify capacitance linearly, whereas sensor residues of voltage-dependent proteins can modify capacitance nonlinearly. Here, we examined the effects of fast temperature jumps induced by an infrared (IR) laser in control and prestin (SLC26a5)-transfected human embryonic kidney (HEK) cells under whole-cell voltage clamp. Prestin's voltage sensor imparts a characteristic bell-shaped, voltage-dependent nonlinear capacitance (NLC). Temperature jumps in control HEK cells cause a monophasic increase in membrane capacitance (Cm) regardless of holding voltage due to double-layer effects. Prestin-transfected HEK cells, however, additionally show a biphasic increase/decrease in Cm with a reversal potential corresponding to the voltage at peak NLC of prestin (Vh), attributable to a rapid temperature-following shift in Vh, with shift rates up to 14 V/s over the course of a 5 ms IR pulse. Treatment with salicylate, a known inhibitor of NLC, reestablishes control cell behavior. A simple kinetic model recapitulates our biophysical observations. These results verify a voltage-dependent protein's ability to respond to fast temperature perturbations on a par with double-layer susceptibility. This likely arises from prestin's unique ability to move sensor charge at kilohertz rates, which is required for the outer hair cells' role as a cochlear amplifier.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / metabolism*
  • Electric Capacitance
  • HEK293 Cells
  • Humans
  • Infrared Rays*
  • Kinetics
  • Lasers*
  • Models, Biological
  • Sulfate Transporters
  • Temperature

Substances

  • Anion Transport Proteins
  • SLC26A5 protein, human
  • Sulfate Transporters