Melting in multilayer adsorbed films

We present both an improved model and new experimental data concerning the problem of melting in multilayer adsorbed films. The model treats in a mutually consistent manner all interfaces in a stratified film. This results in the prediction of substrate freezing, a phenomenon thermodynamically analogous to surface melting. We also compare the free energies of stratified films to those of homogeneous films. This leads to an orderly classification of multilayer phase diagrams in the vicinity of the bulk triple point. The results of the model are compared with the experimentally known systems. Of these, only methane/graphite exhibits melting from homogeneous solid to homogeneous liquid in multilayer films. The systems Ne/graphite and Ar/graphite, studied by Zhu and Dash, exhibit surface melting and substrate freezing instead. We observe experimentally, by means of pulsed nuclear magnetic resonance, that melting in methane adsorbed on graphite extends below the film thickness at which the latent heat of melting is known to vanish. The multilayer melting curve in this system is a first-order prewetting transition, extending from triple-point dewetting at bulk coexistence down to a critical point where the latent heat vanishes at about four layers, and apparently extending to thinner films as a higher-order, two-dimensional phase transition. It would therefore seem that methane/graphite is an ideal system in which to study the evolution of melting from two dimensions to three dimensions

Heat capacity of multilayer methane on graphite: Phase transitions in the first four layers

We present high-resolution heat-capacity data for methane adsorbed on graphite for nominal coverages of 0.87 to 7 layers, from T = 70 to 120 K. For films thicker than 1.1 layers, we find capillary condensate coexisting with the film. We have performed heat-capacity scans on films formed by both adsorption and desorption. By comparing the locations of the phase transitions in the chemical potential mu vs T plane, we find that there is no significant interaction between the film and the capillary condensate. The heat-capacity signals from the films map out an unexpectedly rich set of phenomena for the second, third, and fourth layers, including a two-dimensional triple point and a liquid-gas coexistence region for each layer. The fourth-layer critical temperature we find is lower than previous values found by vapor-pressure isotherms

Genetic Predictions of Prion Disease Susceptibility in Carnivore Species Based on Variability of the Prion Gene Coding Region

Mammalian species vary widely in their apparent susceptibility to prion diseases. For example, several felid species developed prion disease (feline spongiform encephalopathy or FSE) during the bovine spongiform encephalopathy (BSE) epidemic in the United Kingdom, whereas no canine BSE cases were detected. Whether either of these or other groups of carnivore species can contract other prion diseases (e.g. chronic wasting disease or CWD) remains an open question. Variation in the host-encoded prion protein (PrP(C)) largely explains observed disease susceptibility patterns within ruminant species, and may explain interspecies differences in susceptibility as well. We sequenced and compared the open reading frame of the PRNP gene encoding PrP(C) protein from 609 animal samples comprising 29 species from 22 genera of the Order Carnivora; amongst these samples were 15 FSE cases. Our analysis revealed that FSE cases did not encode an identifiable disease-associated PrP polymorphism. However, all canid PrPs contained aspartic acid or glutamic acid at codon 163 which we propose provides a genetic basis for observed susceptibility differences between canids and felids. Among other carnivores studied, wolverine (Gulo gulo) and pine marten (Martes martes) were the only non-canid species to also express PrP-Asp163, which may impact on their prion diseases susceptibility. Populations of black bear (Ursus americanus) and mountain lion (Puma concolor) from Colorado showed little genetic variation in the PrP protein and no variants likely to be highly resistant to prions in general, suggesting that strain differences between BSE and CWD prions also may contribute to the limited apparent host range of the latter

The POM Monoclonals: A Comprehensive Set of Antibodies to Non-Overlapping Prion Protein Epitopes

PrPSc, a misfolded and aggregated form of the cellular prion protein PrPC, is the only defined constituent of the transmissible agent causing prion diseases. Expression of PrPC in the host organism is necessary for prion replication and for prion neurotoxicity. Understanding prion diseases necessitates detailed structural insights into PrPC and PrPSc. Towards this goal, we have developed a comprehensive collection of monoclonal antibodies denoted POM1 to POM19 and directed against many different epitopes of mouse PrPC. Three epitopes are located within the N-terminal octarepeat region, one is situated within the central unstructured region, and four epitopes are discontinuous within the globular C-proximal domain of PrPC. Some of these antibodies recognize epitopes that are resilient to protease digestion in PrPSc. Other antibodies immunoprecipitate PrPC, but not PrPSc. A third group was found to immunoprecipitate both PrP isoforms. Some of the latter antibodies could be blocked with epitope-mimicking peptides, and incubation with an excess of these peptides allowed for immunochromatography of PrPC and PrPSc. Amino-proximal antibodies were found to react with repetitive PrPC epitopes, thereby vastly increasing their avidity. We have also created functional single-chain miniantibodies from selected POMs, which retained the binding characteristics despite their low molecular mass. The POM collection, thus, represents a unique set of reagents allowing for studies with a variety of techniques, including western blotting, ELISA, immunoprecipitation, conformation-dependent immunoassays, and plasmon surface plasmon resonance-based assays

Complex folding and misfolding effects of deer-specific amino acid substitutions in the β2-α2 loop of murine prion protein

The β2–α2 loop of PrPC is a key modulator of disease-associated prion protein misfolding. Amino acids that differentiate mouse (Ser169, Asn173) and deer (Asn169, Thr173) PrPC appear to confer dramatically different structural properties in this region and it has been suggested that amino acid sequences associated with structural rigidity of the loop also confer susceptibility to prion disease. Using mouse recombinant PrP, we show that mutating residue 173 from Asn to Thr alters protein stability and misfolding only subtly, whilst changing Ser to Asn at codon 169 causes instability in the protein, promotes oligomer formation and dramatically potentiates fibril formation. The doubly mutated protein exhibits more complex folding and misfolding behaviour than either single mutant, suggestive of differential effects of the β2–α2 loop sequence on both protein stability and on specific misfolding pathways. Molecular dynamics simulation of protein structure suggests a key role for the solvent accessibility of Tyr168 in promoting molecular interactions that may lead to prion protein misfolding. Thus, we conclude that ‘rigidity’ in the β2–α2 loop region of the normal conformer of PrP has less effect on misfolding than other sequence-related effects in this region