ToxDL: deep learning using primary structure and domain embeddings for assessing protein toxicity.

MOTIVATION: Genetically engineering food crops involves introducing proteins from other species into crop plant species or modifying already existing proteins with gene editing techniques. In addition, newly synthesized proteins can be used as therapeutic protein drugs against diseases. For both research and safety regulation purposes, being able to assess the potential toxicity of newly introduced/synthesized proteins is of high importance. RESULTS: In this study, we present ToxDL, a deep learning-based approach for in silico prediction of protein toxicity from sequence alone. ToxDL consists of (i) a module encompassing a convolutional neural network that has been designed to handle variable-length input sequences, (ii) a domain2vec module for generating protein domain embeddings and (iii) an output module that classifies proteins as toxic or non-toxic, using the outputs of the two aforementioned modules. Independent test results obtained for animal proteins and cross-species transferability results obtained for bacteria proteins indicate that ToxDL outperforms traditional homology-based approaches and state-of-the-art machine-learning techniques. Furthermore, through visualizations based on saliency maps, we are able to verify that the proposed network learns known toxic motifs. Moreover, the saliency maps allow for directed in silico modification of a sequence, thus making it possible to alter its predicted protein toxicity. AVAILABILITY AND IMPLEMENTATION: ToxDL is freely available at http://www.csbio.sjtu.edu.cn/bioinf/ToxDL/. The source code can be found at https://github.com/xypan1232/ToxDL. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Fluorescence anisotropy: from single molecules to live cells.

The polarization of light emitted by fluorescent probes is an easily accessible physical quantity that is related to a multitude of molecular parameters including conformation, orientation, size and the nanoscale environment conditions, such as dynamic viscosity and temperature. In analytical biochemistry and analytical chemistry applied to biological problems, fluorescence anisotropy is widely used for measuring the folding state of proteins and nucleic acids, and the affinity constant of ligands through titration experiments. The emphasis of this review is on new multi-parameter single-molecule detection schemes and their bioanalytical applications, and on the use of ensemble polarization assays to study binding and conformational dynamics of proteins and aptamers and for high-throughput discovery of small-molecule drugs.

A mixed film composed of oligonucleotides and poly(2-hydroxyethyl methacrylate) brushes to enhance selectivity for detection of single nucleotide polymorphisms.

Preliminary studies of mixed films composed of oligonucleotides and poly(2-hydroxyethyl methacrylate) (PHEMA) have recently been shown to enhance the selectivity for detection of 3 base-pair mismatched (3 bpm) oligonucleotide targets. Evaluation of selectivity for detection of single nucleotide polymorphisms (SNP) using such mixed films has now been completed. The selectivity was quantitatively determined by considering the sharpness of melt curves and melting temperature differences (DeltaT(m)) for fully complementary targets and SNPs. Stringency conditions were investigated, and it was determined that the selectivity was maximized when a moderate ionic strength was used (0.1-0.6 M). Increases of DeltaT(m) when using mixed films were up to 3-fold larger compared to surfaces containing only immobilized oligonucleotide probes. Concurrently, increases in sharpness of melt curves for 1 bpm targets were observed to be up to 2-fold greater for mixed films. The co-immobilization of PHEMA resulted in a more homogeneous distribution of oligonucleotide probes on surfaces. Lifetime measurements of fluorescence emission from immobilized oligonucleotide probes labeled with Cy3 dye indicated the difference in microenvironment of immobilized oligonucleotides in the presence of PHEMA.