Actin binding proteins (ABPs) are essential players in cytoskeleton dynamics by acting cooperatively to define the spatial separation and organization of filament branching, elongation and nucleation, as well as actin assembly and disassembly processes [4].
As discussed above, studies have implicated NEK2A in the regulation of centrosome separation, microtubule organization, chromatin condensation, SAC, and chromosome congression during cell division.
Using BLSOM for di-, tri- and tetrapeptide compositions, we developed a system to enable separation (self-organization) of proteins by function.
The resulting BLSOM revealed the clear separation (self-organization) of genomic fragments according to phylotypes.
We searched the BLSOM condition to faithfully reproduce separation (self-organization) of function-known proteins according to functional categories.
Oligonucleotide compositions, however, are inevitably affected by mononucleotide composition, and therefore, separation (self-organization) accomplished on oligonucleotide BLSOMs should be significantly affected by the host-dependent mononucleotide composition.
We have applied BLSOM to protein sequence studies to analyze the frequency of oligopeptides and found the separation (self-organization) of proteins according to their functions [ 22].
Unfortunately for me, I was never free to discuss the circumstances that warranted his separation from the organization.
Polarized optical microscopy of bulk materials and pyrene fluorescence emission of polymer water solutions highlighted the copolymer tendency to phase separation and self-organization, respectively.
We then discuss the current knowledge of how a cell can interact with a substrate at the nanoscale and the effect of size, morphology, organization and separation of nanofeatures on cell response.
