14 research outputs found
Downsizing a human inflammatory protein to a small molecule with equal potency and functionality
A significant challenge in chemistry is to rationally reproduce the functional potency of a protein in a small molecule, which is cheaper to manufacture, non-immunogenic, and also both stable and bioavailable. Synthetic peptides corresponding to small bioactive protein surfaces do not form stable structures in water and do not exhibit the functional potencies of proteins. Here we describe a novel approach to growing small molecules with protein-like potencies from a functionally important amino acid of a protein. A 77-residue human inflammatory protein (complement C3a) important in innate immunity is rationally transformed to equipotent small molecules, using peptide surrogates that incorporate a turn-inducing heterocycle with correctly positioned hydrogen-bond-accepting atoms. Small molecule agonists (molecular weigh
Teaching: Natural or Cultural?
In this chapter I argue that teaching, as we now understand the term, is historically and cross-culturally very rare. It appears to be unnecessary to transmit culture or to socialize children. Children are, on the other hand, primed by evolution to be avid observers, imitators, players and helpers—roles that reveal the profoundly autonomous and self-directed nature of culture acquisition (Lancy in press a). And yet, teaching is ubiquitous throughout the modern world—at least among the middle to upper class segment of the population. This ubiquity has led numerous scholars to argue for the universality and uniqueness of teaching as a characteristically human behavior. The theme of this chapter is that this proposition is unsustainable. Teaching is largely a result of recent cultural changes and the emergence of modern economies, not evolution
7α-Hydroxycholesterol induces monocyte/macrophage cell expression of interleukin-8 via C5a receptor
Major phytoplasma diseases of forest and urban trees
In the northern hemisphere, yellows, witches’ broom, and decline diseases
of several forest and urban tree species are widespread and of considerable
economic and ecological significance. Elm (Ulmus spp.) and alder (Alnus spp.) are
affected by elm yellows (EY) and alder yellows (ALY), respectively. These diseases
are mainly associated with the presence of closely related phytoplasmas, the EY
agent ‘Candidatus Phytoplasma ulmi’ and the ALY agent, which are members of
the EY or 16SrV group, subgroups 16SrV-A and 16SrV-C, respectively. Ash
(Fraxinus spp.) is affected by ash yellows, a disease which occurs mainly in North
America and is associated with the presence of ‘Candidatus Phytoplasma fraxini’,
a member of subgroup 16SrVII-A. Poplar (Populus spp.), sandal (Santalum album),
paulownia (Paulownia spp.), and mulberry (Morus spp.) are affected by yellows
diseases associated with phytoplasmas of different 16SrI subgroups. Several species
of conifers are affected by yellows and witches’ broom diseases associated with
phytoplasmas belonging to at least five taxonomic groups (16SrI, 16SrIII, 16SrVI,
16SrIX, and 16SrXXI) and several different subgroups. A number of urban tree species
grown in the Sabana de Bogotà (Colombia) are affected by decline diseases
which are primarily associated with 16SrI and 16SrVII phytoplasmas. This chapter
summarizes the current knowledge of major phytoplasma diseases of forest and
urban trees grown in the northern hemisphere