Dynamic states of biopolymers are associated with appearance and disap
pearance of spaces, or voids, to an extent larger than what is hithert
o recognized. Current awareness of the existence of free space in biop
olymers is by and large restricted in terms of (i) essentially small p
ores obeying Boltzman distribution of sizes and energy and (ii) rigid
structures dictated by structural constraints, whose volume merely exh
ibits fluctuations within the thermal limits. Interconnectivity of the
se spaces within biopolymers such as membranes gives rise to new possi
bilities in addressing some of the long standing problems in understan
ding catalysis, transport and the derived biological phenomena. Given
the a priori recognition that other kinds of spaces can exist in biopo
lymers, which are dynamic, predominantly inducible and possibly larger
, a new kind of experimentation becomes possible as also a new set of
constraints for the acceptability of molecular models of interactions
in the explanation of biological phenomena. The theory of adsorption o
f liquids and presence of structural cavities as exemplified by zeolit
es competently accounts for; much of the current thinking in our under
standing of cavities in biopolymers. Induction of (larger) voids requi
res approaches that are significantly different. We suggest that it is
necessary to consider a reservoir of inner space as a specific contri
bution to the energetics of polymer dynamics. We outline a methodologi
cal approach that helps identify these voids as well as biological phe
nomena in which the notion of dynamics of voids would bring novel insi
ghts. (C) 1998 Academic Press.