Flexgrepps--flexible greedy peptide pool search: computation of near-optimal sets of degenerate polypeptides for antigenic screening.

Although synthesizing and utilizing individual peptides and DNA primers has become relatively inexpensive, massively parallel probing and next-generation sequencing approaches have dramatically increased the number of molecules that can be subjected to screening; this, in turn, requires vast numbers of peptides and therefore results in significant expenses. To alleviate this issue, pools of related molecules are often used to downselect prior to testing individual sequences. A computational selection process to create pools of related sequences at large scale has not been reported for peptides.

Exploring the protein landscape in ramachandran space: it's not just psi-phi.

Most methods for the structural comparison of proteins utilize molecular coordinates in the three-dimensional physical space. Recently, a group has presented an elegant novel approach based on the characterization of protein shape in terms of backbone torsion angles. They have demonstrated considerable success in direct comparisons with other techniques, and their method lends itself to rapid screening of structural information from rapidly growing databases.

Searching for transcription factor binding site clusters: how true are true positives?

The computational detection of functional transcription factor binding sites in genomic sequence is one of the challenges of the post-genomic era. Several groups have approached this problem from different directions and have demonstrated considerable success. The purpose of this communication, however, is to point out an imperfection in the way computational results are commonly reported that may lead to a distorted picture of the performance of existing algorithms.

In silico identification of metazoan transcriptional regulatory regions.

Transcriptional regulation remains one of the most intriguing and challenging subjects in biomedical research. The catalysis of transcription is a clear example of multiple proteins interacting to orchestrate a biological process, offering a starting point for the study of biological systems. Transcriptional regulation is viewed as one of the principal mechanisms governing the spatial and temporal distribution of gene expression, thus the field of transcriptional regulation provides a natural stage for quantitative studies of multiple gene systems.

IL-28, IL-29 and their class II cytokine receptor IL-28R.

Cytokines play a critical role in modulating the innate and adaptive immune systems. Here, we have identified from the human genomic sequence a family of three cytokines, designated interleukin 28A (IL-28A), IL-28B and IL-29, that are distantly related to type I interferons (IFNs) and the IL-10 family. We found that like type I IFNs, IL-28 and IL-29 were induced by viral infection and showed antiviral activity.