Second-harmonic
light scattering (SHS) permits characterization
of membrane-specific molecular transport in living cells. Herein,
we demonstrate the use of time-resolved SHS for quantifying chemically
induced enhancements in membrane permeability. As proof of concept,
we examine the enhanced permeability of the cytoplasmic membrane in
living <i>Escherichia coli</i> following addition of extracellular
adenosine triphosphate (ATPe). The transport rate of the hydrophobic
cation, malachite green, increases nearly an order of magnitude following
addition of 0.1 mM ATPe. The absence of an ATPe-enhanced permeability
in liposomes strongly suggests the induced effect is protein-mediated.
The utility of SHS for elucidating the mechanism of action of antimicrobials
is discussed