Methionine adenosyltransferase (MAT), a key enzyme in metabolism, cata
lyzes the synthesis of one of the most important and pivotal biologica
l molecules, S-adenosylmethionine. In every organism studied thus far,
MAT exists in multiple forms; most are encoded by related, but distin
ct genes. Molecular and immunological studies revealed the presence of
considerable conservation in the structure of MAT from different spec
ies; however, the various MAT isozymes differ in their physical and ki
netic properties in ways that allow them to be regulated differently.
Recent studies suggest that human MAT is composed of nonidentical subu
nits that can assume multiple states of aggregation, each with differe
nt kinetic characteristics. The tissue distribution of MAT isozymes an
d the ability of cells within the same tissue to switch between the di
fferent forms of MAT suggest that this mode of regulation is important
for cellular function and differentiation. Therefore, understanding t
he regulation and structure-function relationship of this fascinating
enzyme should help us clarify its role in biology and may provide us w
ith tools to effectively manipulate its activity in clinical situation
s such as cancer, autoimmunity and organ transplantation.