Optical Control of Antibody Activity by Using Photocleavable Bivalent Peptide–DNA Locks

Antibody-based molecular recognition plays a central role in today's life sciences, ranging from immunoassays to molecular imaging and antibody-based therapeutics. Control over antibody activity by using external triggers such as light could further increase the specificity of antibody-based targeting. Here we present bivalent peptide–DNA ligands containing photocleavable linkers as a noncovalent approach by which to allow photoactivation of antibody activity. Light-triggered cleavage of the 3-amino-3-(2-nitrophenyl)propionic acid peptide linker converted the high-affinity bivalent peptide–DNA lock into weakly binding monovalent ligands, effectively restoring antibody targeting of cell-surface receptors. In this work, a proof of principle was provided with an anti-hemagglutinin antibody, but the molecular design of the lock is generic and applicable to any monoclonal antibody for which an epitope or mimotope of sufficient affinity is available.     

Mesophase features in isotactic poly(propylene‐co‐1‐heptene) copolymers

The influence of crystallization rate on the interesting polymorphism of random isotactic poly(propylene‐co‐1‐heptene) copolymers was studied, with particular attention to the conditions for obtaining the mesomorphic phase. Owing to the important decrease of cooling rate involved as the 1‐heptene content increases, the mesophase can be clearly observed by DSC for co‐unit contents above about 5 mol%. Furthermore, only the mesophase (or the amorphous phase) was found for the copolymer with 13.9 mol% 1‐heptene at common cooling rates of the calorimeter. Additionally, the copolymer with 21.4 mol% co‐units was found to be completely amorphous under any thermal treatment analyzed. Variable‐temperature diffraction experiments were carried out to ascertain unambiguously the nature of the phases involved. Finally, a remarkable transparency was attained (above 80% transmittance in the visible light region) at intermediate and high 1‐heptene contents, using easily accessible cooling rates. © 2016 Society of Chemical Industry     

Environmental stress cracking of polyvinyl chloride compounds under long-term stress

Polyvinyl chloride compounds rupture prematurely in contact with environmental stress cracking (ESC) agents such as plasticizers. This effect shows a considerable deviation in a stress rupture plot (log stress vs log time) from the expected stress rupture in the absence of ESC agents. PVC and polymers in general dilate under a stress, increase free volume, and allow diffusion of the ESC agent and plasticization of the polymer. However, we show ESC failure is not dependent alone on molecular size of the ESC agent when comparing di-2-ethylhexyl adipate (DOA), di-2-ethylhexyl phthalate (DOP), and tri-2-ethylhexyl trimelitate (TOTM). Therefore this suggests that ESC failure is not strictly associated with diffusion of the ESC agent into the free volume of the PVC, but rather flaws and stress concentrations play a large role. Higher molecular weight PVC retards rupture, both in air and in contact with the ESC agent. However, the safe way to design PVC parts is to avoid ESC contact with stressed PVC rather than using high molecular weight PVC. Part design can play an important role in preventing these premature failures by keeping the ESC agent away from contact with stressed PVC.     

Biological properties of three Mexican isolates of Aujeszky's disease virus

Four strains of Aujeszky's Disease virus (ADV) were included in this study; three Mexican field isolates (215,145 and C-8) in conjunction with the Shope reference strain of ADV, which has known pathogenic characteristics. All four strains were included in each treatment, which consisted of heat treatment, trypsin treatment and passed ten times on chicken embryo fibroblasts. Both virus titer and plaque size were determined on the first and tenth passage and on treated and untreated strains. On each of the treatments, the plaque size had significant differences (p = 0.001) which had relation to the two factors studied, namely strain and passage level. There was no significant variation related to the type of treatment between strains. With the strains under study, the authors also made rabbit pathogenicity tests, and it was found that on passage one, the strains caused clear nervous symptoms and death, while on the tenth passage level, the Mexican strains produced slight pruritus, few nervous symptoms and allowed the rabbits to survive. The mouse test revealed an increased median death time after the treatments, as well as a large increase in standard deviations. These data are interpreted as an increased heterogeneity of the strains in all of the treatments to the strains of viruses.     

The use of neurophysiopathological technics in assessing pain syndromes in industrial medicine and rehabilitation

The use of neurophysiopathological techniques in the assessment of pain syndromes in occupational and rehabilitative medicine. Pain is one the major causes of disability. In occupational medicine this is translated into a loss of working days or the need to change jobs. In rehabilitation pain limits treatment and often lengthens recovery time. Neurophysiopathological techniques can be used to improve neuroalgological diagnosis and gain better understanding of pathogenic mechanisms thus allowing therapy to be targeted more precisely aiding the subject's social and occupational recovery.     

On the stability of the one-step exact collocation method for the second kind volterra integral equation with degenerate kernel

The local stability properties of the collocation method applied to a second kind Volterra integral equation with degenerate kernel are investigated. A finite length recurrence relation is derived and theorems for the local stability of the methods are proved.     

Isoflurane anesthesia blunts cerebral responses to noxious and innocuous stimuli: a fMRI study

We used functional magnetic resonance imaging to determine how isoflurane affected cerebral neuronal activation resulting from noxious and innocuous stimuli. Five male volunteers were subjected to mild electrical shock and tactile stimuli applied to the hand. During low (0.7%) and moderate (1.3%) isoflurane anesthesia the stimuli were repeated and a supramaximal electrical shock was also applied. Tactile stimulation activated bilateral SI and SII, but resulted in no significant activation at low or moderate anesthesia. Electrical shock activated contralateral SI and bilateral SII; low anesthesia completely abolished this response. The supramaximal stimulus activated the caudate nucleus and bilateral thalamus at low anesthesia; these responses were diminished at moderate anesthesia. Isoflurane anesthesia blunts cerebral responses to somatosensory stimuli, and the absence of cortical activation during supramaximal stimulation suggests that noxious-induced movement is generated in lower CNS structures.     

Gas chromatograph/isotope dilution mass spectrometric analysis of airborne benzo

A critical evaluation has been made of the gas chromatography/isotope dilution mass spectrometry (GC/IDMS) analysis of airborne benzo[a]pyrene (B[a]p) using 2H-(deuterium, D) and 13C-labeled benzo[a]pyrene and a low resolution mass spectrometer. Laboratory quality control and field samples were used to determine the suitability of these two isotopically labeled B[a]p as surrogates for GC/IDMS B[a]p analysis. With method spike QC samples, recovery of the B[a]p was compared with the recoveries of D- and 13C-labeled B[a]p to validate the assumption that these two isotopically labeled B[a]p analogs could be used as method surrogates for IDMS B[a]p analyses. Two collocated Anderson Hi-Vol samplers were used to carry out a field study in which total B[a]p loadings from one sampler were correlated to the second sampler, before and after correcting the total B[a]p loadings against the recovery of the D- and 13C-labeled B[a]p. It is shown that a low-resolution mass spectrometer can be used in GC/IDMS B[a]p analysis to achieve results of high precision and accuracy. Depending on data quality objectives, D-labeled B[a]p could be used for IDMS B[a]p analysis, but is not recommended.