posted on 2012-09-05, 00:00authored byHideyuki Miyatake, Naoshi Dohmae
In this study, a solution circulating apparatus was employed
to
control the aggregation of protein molecules in situ. The association
state of protein molecules was controlled by injecting protein solutions,
buffers, and solutes into the device while monitoring the heterodispersity
of the molecular nanoaggregates by an apparatus of high-performance
heterodyne-based dynamic light scattering. Further, a highly ordered
association of protein nanoaggregates was induced that lead to the
generation and growth of protein crystals suitable for structural
analysis by the X-ray protein crystallography. We could also dissociate
protein molecules that had already formed aggregates into mono- or
bimodal states and reassociate them to form protein crystals, which
contribute to minimizing the amount of protein required for crystallization.
Our nanotechnological approach allowed us to carefully monitor and
control crystal growth with a focus on the association state of the
target proteins. The high-performance DLS device monitors the in situ
association process of the target proteins allowing a dynamic response
to modify the solution properties and leading to a deeper understanding
of protein crystallization and achieving rational control of the processes.