From Wikipedia,
the free encyclopedia.
- HTS redirects here, it can
also reffer to the "horizontal
tab set" control code in the
C1 control code set.
High-throughput screening,
often abbreviated as HTS,
is a method for scientific
experimentation especially
relevant to the fields of
biology and
chemistry. Through a
combination of modern
robotics and other specialized
laboratory hardware, it allows a
researcher to effectively conduct
hundreds of scientific experiments
at once.
In essence, HTS uses a
brute-force approach to
collect a large amount of
experimental data -- usually
observations about how some
biological entity reacts to
exposure to various chemical
compounds -- in a relatively short
time. A screen, in this
context, is the larger experiment,
with a single goal (usually
testing a
scientific hypothesis), to
which all this data may
subsequently be applied.
A key piece of HTS equipment is
a plate: a small container,
usually made of plastic, that
features a grid of small, open
divots called wells. Most
of the wells contain
experimentally useful matter,
often a
solution of
dimethyl sulfoxide (DMSO) and
some other
chemical compound, the latter
of which is different for each
well across the plate. (The other
wells are empty, intended for use
as optional experimental
controls.)
To prepare for an assay, the
researcher fills each well of the
plate with some biological entity
that he or she wishes to conduct
the experiment upon, such as a
protein, some
cells, or an animal
embryo. After some
incubation time has passed to
allow the biological matter to
absorb, bind to, or otherwise
react (or fail to react) with the
compounds in the wells,
measurements are taken across all
the plate's wells, either manually
or by a machine. Manual
measurements are often necessary
when the researcher is using
microscopy to (for example)
seek changes or defects in
embryonic development caused by
the wells' compounds, looking for
effects that a computer could not
easily determine by itself.
Otherwise, a specialized automated
analysis machine can run a number
of experiments on the wells (such
as shining polarized light on them
and measuring reflectivity, which
can be an indication of protein
binding). In this case, the
machine outputs the result of each
experiment as a grid of numeric
values, with each number mapping
to the value obtained from a
single well. A high-capacity
analysis machine can measure
dozens of plates in the space of a
few minutes like this, generating
thousands of experimental
datapoints very quickly.
Depending upon the results of
this first assay, the researcher
can perform followup assays within
the same screen by "cherrypicking"
liquid from the wells that gave
interesting results (known as
"hits") into new assay plates, and
then re-running the experiment to
collect further data on this
narrowed set, confirming and
refining observations.
A screening facility typically
holds a library of stock plates,
whose contents are carefully
catalogued, and each of which may
have been created by the lab or
obtained from a commercial source.
These stock plates themselves are
not directly used in experiments;
instead, separate assay plates
are created as needed. An assay
plate is simply a copy of a stock
plate, created by
pipetteing a small amount of
liquid (often measured in
nanoliters) from from the
wells of a stock plate to the
corresponding wells of a
completely empty plate.
Automation is an important
element in HTS's usefulness. A
specialized
robot is often responsible for
much of the process over the
lifetime of a single assay plate,
from creation through final
analysis. An HTS robot can usually
prepare and analyze many plates
simultaneously, further speeding
the data-collection process. HTS
robots currently exist which can
test up to 100 000 compounds per
day (Hann 2004).
HTS is a relatively recent
innovation, made lately feasible
through modern advances in
robotics and high-speed computer
technology. It still takes a
highly specialized and expensive
screening lab to run an HTS
operation, however, so in many
cases a small-to-moderately sized
research institution will use the
services of an existing HTS
facility rather then set up one
for itself.
References
Hann, M.M., Oprea, T.I.
Pursuing the leadlikeness concept
in parmaceutical research. Current
Opinion in Chemical Biology. 2004,
8, 255-263.