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Biology subjects

Gaeta, B.

Publications and source records attributed to Gaeta, B..

2 recordsLinked to original sources

Machine learning prediction of Antibody-Antigen binding: dataset, method and testing

DNA sequencing technologies are providing new insights into the immune response by allowing the large scale sequencing of rearranged immunoglobulin gene present in an individual, however the applications of this approach are limited by the lack of methods for determining the antigen(s) that an immunoglobulin encoded by a given sequence binds to. Computational methods for predicting antibody-antigen interactions that leverage structure prediction and docking have been proposed, however these methods require knowledge of the 3D structures. As a step towards the development of a machine learning method suitable for predicting antibody-antigen binding affinities from sequence data, a weighted nearest neighbor machine learning approach was applied to the problem. A prediction program was coded in Python and evaluated using cross-validation on a dataset of 600 antibodies interacting with 50 antigens. The classification predicting accuracy was around 76% for this dataset. These results provide a useful frame of reference as well as protocols and considerations for machine learning and dataset creation in this area. Both the dataset (in csv format) and the machine learning program (coded in python) are freely available for download.

bioinformatics↗

WRN Helicase is a Synthetic Lethal Target in Microsatellite Unstable Cancers

Summary paragraphSynthetic lethality, an interaction whereby the co-occurrence of two or more genetic events lead to cell death but one event alone does not, can be exploited to develop novel cancer therapeutics1. DNA repair processes represent attractive synthetic lethal targets since many cancers exhibit an impaired DNA repair pathway, which can lead these cells to become dependent on specific repair proteins2. The success of poly (ADP-ribose) polymerase 1 (PARP-1) inhibitors in homologous recombination-deficient cancers highlights the potential of this approach in clinical oncology3,4. Hypothesizing that other DNA repair defects would give rise to alternative synthetic lethal relationships, we asked if there are specific dependencies in cancers with microsatellite instability (MSI), which results from impaired DNA mismatch repair (MMR). Here we analyzed data from large-scale CRISPR/Cas9 knockout and RNA interference (RNAi) silencing screens and found that the RecQ DNA helicase WRN was selectively essential in MSI cell lines, yet dispensable in microsatellite stable (MSS) cell lines. WRN depletion induced double-strand DNA breaks and promoted apoptosis and cell cycle arrest selectively in MSI models. MSI cancer models specifically required the helicase activity, but not the exonuclease activity of WRN. These findings expose WRN as a synthetic lethal vulnerability and promising drug target in MSI cancers.

cancer biology↗