Structural proteins of the membrane skeleton are thought to form ''cor
rals'' at the membrane surface, and these corrals may restrict lateral
diffusion of membrane proteins. Recent experimental developments in s
ingle-particle tracking and laser trapping make it possible to examine
the corral model in detail. Techniques to interpret these experiments
are presented. First, escape times for a diffusing particle in a corr
al are obtained from Monte Carlo calculations and analytical solutions
for various corral sizes, shapes, and escape probabilities, and reduc
ed to a common curve. Second, the identification of corrals in trackin
g experiments is considered. The simplest way to identify corrals is b
y sight. If the walls are impermeable enough, a trajectory fills the c
orral before the diffusing particle escapes. The fraction of distinct
sites visited before escape is calculated for corrals of various sizes
, shapes, and escape probabilities, and reduced to a common curve. Thi
s fraction is also a measure of the probability that the diffusing spe
cies will react with another species in the corral before escaping. Fi
nally, the effect of the sampling interval on the measurement of the s
hort-range diffusion coefficient is examined.