100 research outputs found
Traveling spatially periodic forcing of phase separation
We present a theoretical analysis of phase separation in the presence of a
spatially periodic forcing of wavenumber q traveling with a velocity v. By an
analytical and numerical study of a suitably generalized 2d-Cahn-Hilliard model
we find as a function of the forcing amplitude and the velocity three different
regimes of phase separation. For a sufficiently large forcing amplitude a
spatially periodic phase separation of the forcing wavenumber takes place,
which is dragged by the forcing with some phase delay. These locked solutions
are only stable in a subrange of their existence and beyond their existence
range the solutions are dragged irregularly during the initial transient period
and otherwise rather regular. In the range of unstable locked solutions a
coarsening dynamics similar to the unforced case takes place. For small and
large values of the forcing wavenumber analytical approximations of the
nonlinear solutions as well as for the range of existence and stability have
been derived
Into the unknown: expression profiling without genome sequence information in CHO by next generation sequencing
The arrival of next-generation sequencing (NGS) technologies has led to novel opportunities for expression profiling and genome analysis by utilizing vast amounts of short read sequence data. Here, we demonstrate that expression profiling in organisms lacking any genome or transcriptome sequence information is feasible by combining Illumina’s mRNA-seq technology with a novel bioinformatics pipeline that integrates assembled and annotated Chinese hamster ovary (CHO) sequences with information derived from related organisms. We applied this pipeline to the analysis of CHO cells which were chosen as a model system owing to its relevance in the production of therapeutic proteins. Specifically, we analysed CHO cells undergoing butyrate treatment which is known to affect cell cycle regulation and to increase the specific productivity of recombinant proteins. By this means, we identified sequences for >13 000 CHO genes which added sequence information of ∼5000 novel genes to the CHO model. More than 6000 transcript sequences are predicted to be complete, as they covered >95% of the corresponding mouse orthologs. Detailed analysis of selected biological functions such as DNA replication and cell cycle control, demonstrated the potential of NGS expression profiling in organisms without extended genome sequence to improve both data quantity and quality
The mechanisms of boronate ester formation and fluorescent turn-on in ortho-aminomethylphenylboronic acids
ortho-Aminomethylphenylboronic acids are used in receptors for carbohydrates and various other compounds containing vicinal diols. The presence of the o-aminomethyl group enhances the affinity towards diols at neutral pH, and the manner in which this group plays this role has been a topic of debate. Further, the aminomethyl group is believed to be involved in the turn-on of the emission properties of appended fluorophores upon diol binding. In this treatise, a uniform picture emerges for the role of this group: it primarily acts as an electron-withdrawing group that lowers the pK(a) of the neighbouring boronic acid thereby facilitating diol binding at neutral pH. The amine appears to play no role in the modulation of the fluorescence of appended fluorophores in the protic-solvent-inserted form of the boronic acid/boronate ester. Instead, fluorescence turn-on can be consistently tied to vibrational-coupled excited-state relaxation (a loose-bolt effect). Overall, this Review unifies and discusses the existing data as of 2019 whilst also highlighting why o-aminomethyl groups are so widely used, and the role they play in carbohydrate sensing using phenylboronic acids
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