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Surface Proximity Effects on Water and
Solvated IonsSuzi Jarvis
Nanoscale Function Group
Ctr. Research on Adaptive Nanostructures
and Nanodevices, Trinity College
Dublin, Ireland
Water is a prerequisite for life and by far the largest
single component in the living organism and so at the heart of all
studies concerning bio-molecular function. Virtually all cellular
processes including protein folding, immune response and membrane
assembly are influenced by the delicate interplay between hydrophilic
and hydrophobic interactions. And yet hydration forces are probably the
least understood of all fundamental intermolecular forces in liquid and
the subject of much scientific debate.
Directly measuring structural changes in water with a mechanical probe
of lateral dimensions comparable to that of a single molecule provides
an invaluable insight into how and why bio-molecules behave with high
selectivity or why certain surfaces promote or inhibit bio-molecular
adhesion. In the immediate vicinity of the molecule, continuum models
break down and the aqueous environment will often form a discrete
layered structure depending on the nature of the molecule. The absence
or presence of such structure may be of fundamental importance to
molecular functionality.
Due to its highly localized measurement ability, the atomic force
microscope can be applied to characterize the mechanical response of
materials too laterally specific to be investigated by Surface Forces
Apparatus or nano-indentation devices. We have directly measured
localized density changes in ultra-pure water using frequency-modulation
atomic force microscopy (FM-AFM) close to model hydrophilic and
hydrophobic self-assembled monolayers (SAMs), inorganic surfaces and
lipid bilayers and have combined these measurements with nanometer
resolution images of the surfaces. Our findings reveal that solvent
ordering depends on the geometry and chemistry of the two interacting
surfaces while the quantitative force values measured are strongly
dependent on sample compliance. |