Easy access to triazolinedione-endcapped peptides for chemical ligation.

An efficient and easy route towards triazolinedione (TAD) endcapped peptides is described, in which a TAD-precursor was coupled to N-terminal amines on a solid support. Modified peptides readily reacted with diene end-functionalized poly(ε-caprolactone) of different molecular weights. The ligation proved to be orthogonal to a variety of functional groups present in natural amino acids.

Design of mixed PEO/PAA brushes with switchable properties toward protein adsorption.

Adsorption of proteins at interfaces is an ubiquitous phenomenon of prime importance. Layers of poly(ethylene oxide) (PEO) are widely used to repel proteins. Conversely, proteins were shown to adsorb deeply into brushes of poly(acrylic acid) (PAA), and their subsequent partial release could be triggered by a change of pH and/or ionic strength (I). Mixed brushes of these polymers are thus promising candidates to tune protein adsorption onto new smart surfaces. In this work, the synthesis of such mixed brushes was performed based on a "grafting to" approach, the two polymers being either grafted sequentially or simultaneously. Detailed characterization of the obtained brushes using static water contact angle measurements, X-ray photoelectron spectroscopy, electrochemical impedance spectroscopy, and polarization-modulation reflection-absorption infrared spectroscopy is presented. While sequential grafting of the two polymers for different reactions times did not give rise to a broad range of composition of mixed brushes, simultaneous grafting of the polymers from solutions with different compositions allows for the synthesis of a range of mixed brushes (mass fraction of PEO in the mixed brushes from 0.35 to 0.65). A key example is then chosen to illustrate the switchable behavior of a selected mixed PEO/PAA brush toward albumin adsorption. The adsorption behavior was monitored with a quartz crystal microbalance. The mixed brush could adsorb high amounts of albumin, but 86% of the adsorbed protein could then be desorbed upon pH and I change. The obtained properties are thus a combination of the ones of PEO and PAA, and a highly switchable behavior is observed toward protein adsorption.

Pressure-enhanced dynamic heterogeneity in block copolymers of poly(methyl vinyl ether) and poly(isobutyl vinyl ether).

The static structure factor and associated dynamics have been investigated in a series of block copolymers of poly(methyl vinyl ether) (PMVE) and poly(isobutyl vinyl ether) (PiBVE) using x-ray scattering and dielectric spectroscopy (DS). The origin of the dynamic arrest at the glass temperature (T(g)) of PiBVE has been explored by temperature- and pressure-dependent DS and pressure-volume-temperature measurements. Both temperature and volume are responsible for the segmental dynamics but temperature has a stronger effect. The copolymers display a minimal dynamic asymmetry (Delta T(g) approximately 7 K), nevertheless, are spatially and dynamically heterogeneous. Increasing pressure, unlike temperature, enhances the dynamic heterogeneity. This effect originates from the distinctly different pressure sensitivities of the homopolymers and can be traced back to differences in local packing.