Type I allergy is an immunoglobulin E (IgE)-mediated hypersensitivity disease affecting more than 25% of the population. Currently, diagnosis of allergy is performed by provocation testing and IgE serology using allergen extracts. This process defines allergen-containing sources but cannot identify the disease-eliciting allergenic molecules. We have applied microarray technology to develop a miniaturized allergy test containing 94 purified allergen molecules that represent the most common allergen sources. The allergen microarray allows the determination and monitoring of allergic patients' IgE reactivity profiles to large numbers of disease-causing allergens by using single measurements and minute amounts of serum. This method may change established practice in allergy diagnosis, prevention, and therapy. In addition, microarrayed antigens may be applied to the diagnosis of autoimmune and infectious diseases.

The higher plant Arabidopsis thaliana (Arabidopsis) is an important model for identifying plant genes and determining their function. To assist biological investigations and to define chromosome structure, a coordinated effort to sequence the Arabidopsis genome was initiated in late 1996. Here we report one of the first milestones of this project, the sequence of chromosome 4. Analysis of 17.38 megabases of unique sequence, representing about 17% of the genome, reveals 3,744 protein coding genes, 81 transfer RNAs and numerous repeat elements. Heterochromatic regions surrounding the putative centromere, which has not yet been completely sequenced, are characterized by an increased frequency of a variety of repeats, new repeats, reduced recombination, lowered gene density and lowered gene expression. Roughly 60% of the predicted protein-coding genes have been functionally characterized on the basis of their homology to known genes. Many genes encode predicted proteins that are homologous to human and Caenorhabditis elegans proteins.

Monodisperse PMMA beads of a size varying between 200 and 400 nm have been prepared by a modified emulsion polymerization technique. These beads sediment well on substrates to form 3-dimensional face-centered cubic packages. This method allows it to cover large glass substrates (area up to 10 × 10 cm) with an opalescent layer of the beads thus creating films with opaline structure, which can be used as photonic crystals. Choosing PMMA as the material of the beads brings several advantages, e.g., the PMMA photonic films can be precisely patterned by e-beam lithography with the feature resolution down to one bead in width and various fluorescent dyes can be incorporated in PMMA balls. Dye-impregnated PMMA opaline photonic films demonstrate the incomplete photonic band gap structure and related modification of dye photoluminescence spectrum.

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Photonic crystals in the form of large area thin films consisting of closely packed polymethylmethacrylate beads were sedimented on glass substrates. The high ordering of the opaline films made it possible to observe a number of fine features in the optical diffraction, including Fabry-Perot oscillations of the reflectivity and branching of the angular dispersion of the Bragg resonances with increase of the angle of incidence of the light beam. Results of calculations of the photonic band structure and simulations of the reflectance spectra agree well with experimental observations.