Chapter 1 – Introduction 3
physics started around the middle of twentieth century, at a time when several researchers
trained originally from a background of the physical sciences made significant advances
toward the development of what we now call molecular biology. Biophysics as a new dis
cipline was shaped significantly from the combined successes of physiology and structural
biology at around the same time. The former involved, for example, the pioneering work
of Alan Hodgkin and Andrew Huxley, which revealed how the fundamental mechanism of
conduction of sensory signals in nerves is achieved (Hodgkin and Huxley, 1952). The latter
applied emerging physics tools to study the scattering of x-rays from crystals made of bio
logical molecules, first exemplified in the work, from the 1930s onward, of one of the great
women of modern science, Dorothy Hodgkin (née Crowfoot), in her determination of the
structures of a number of biologically important small molecules, including cholesterol,
penicillin, and vitamin B12, but then later on much larger molecules called proteins, first
shown on one found in muscles called myoglobin (Kendrew et al., 1958).
Hodgkin and Huxley’s seminal paper, at the time of my writing this sentence, has been
cited over 16,000 times and deserves its place as one of the pioneering publications of
modern biophysics. To some biomathematicians and physiologists, this might seem contro
versial, since they may claim this paper as one from their own fields, especially since neither
Hodgkin nor Huxley necessarily identified as being a “physicist” (their respective areas of
primary expertise were biochemistry and physiology, respectively). But with the wisdom of
historical hindsight, it is clear that their work sits very much at the cutting-edge interdiscip
linary interface between biology and physics.
The beauty of this exemplar study, in particular, is that it used multiple biophysical tools
to solve a challenging biological question. It investigated the fundamental properties of elec
trical nerve conduction by reducing the problem to being one of the ion channels in cell
membranes (Figure 1.1a) that could be characterized by experimental measurements using
biophysical technology of time-resolved voltage signals by electrodes placed inside and out
side the nerve fiber during a stimulated nerve conduction (Figure 1.1b). But these experi
mental signals could then be modeled using the physics of electrical circuitry (Figure 1.1c),
for example, by modeling the electric current due to ions flowing through an ion channel
in the cell membrane as being equivalent to a resistor in a standard electrical circuit, with a
voltage applied across it, which is equivalent to the voltage across the cell membrane, that is,
the difference in electrical potential per unit charge between the inside of the cell and the out
side of the cell, denoted by Vm, and the cell membrane acting as a dielectric, thus functioning
as a capacitor (discussed in Chapter 2), here of capacitance per unit area Cm. In its simplest
form, the electric current flow I across the cell membrane can be modeled mathematically
as simply
(1.1)
I
C
V
t
I
=
+
m
m
i
d
d
where Ii is the electric current flow through the actual ion channel. This model can be
easily expanded using multiple sets of differential equations to account for multiple different
ion channels (Figure 1.1d), and this also fits the experimental observations very well.
However, the point here of these two approaches is that they illustrate not just the
achievements of new biological insight made with physical science experimental tools
and that they were both coupled closely to advances in methods of physical science analysis
techniques, in the case of nerve conduction to a coupled series of analytical differential
equations called the “Hodgkin–Huxley model,” which describes the physics of the propaga
tion of information in the nerves via electrical conduction of sodium and potassium ions
across the nerves’ outer electrically insulating membranes, an electric phenomenon known
by biologists as the “action potential.” X-ray crystallography, the analysis concerned with
building mathematical tools that could in essence generate the inverse of the x-ray scatter
pattern produced by protein crystals to reveal the underlying spatial coordinates of the con
stituent atoms in the protein molecule, is a process involving Fourier transformation coupled
with additional mathematical techniques for resolving the phase relationship between the