G. Haugstad et Wl. Gladfelter, PROBING BIOPOLYMERS WITH SCANNING FORCE METHODS - ADSORPTION, STRUCTURE, PROPERTIES, AND TRANSFORMATION OF GELATIN ON MICA, Langmuir, 10(11), 1994, pp. 4295-4306
Scanning force microscopy of thin gelatin films on mica reveals two di
stinct film components with characteristic frictional, morphological,
and adsorptive signatures. A high-friction continuous film 1-4 nm thic
k strongly adheres to mica, while a low-friction component is more wea
kly adsorbed as large islands on top of, or small domains within, the
high-friction layer. The low-friction component exhibits a porous morp
hology and fluid-like character and is selectively destroyed when the
film is heated sufficiently. A high-force scanning procedure remarkabl
y transforms the molecularly-rough high-friction film into the molecul
arly-smooth low-friction component if a sufficient amount of water is
present in or on the film. The nanostructure of both the high- and low
-friction components is imaged using a nanometer-scale asperity of gel
atin attached to the SFM tip. The anticipated network structure of gel
atin is observed on the high-friction layer. The low-friction material
is interpreted as moieties of intramolecularly-folded gelatin, with t
hickness (1.5 +/- 0.2 nm) equal to the diameter of the collagen-fold t
riple helix, containing substantial structural water. Analysis suggest
s that differences in viscoelasticity account for the component-specif
ic frictional dissipation.