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El Alaoui, S.

Publications and source records attributed to El Alaoui, S..

2 recordsLinked to original sources

Simulating Iron Deficiency in Plant Plastids With a Flexible Physics-Informed Neural Network Approach

Flux balance analysis has proven to be a successful approach in metabolic engineering and systems biology to predict intracellular fluxes of large genome-scale networks and the essentiality of genes encoding enzymes and regulatory factors. Flux balance analysis (FBA) relies on a key assumption of a metabolic state being persistent ("steady") over a given time frame. This assumption works well for microbial growth because of the ease with which microbial media can be fixed, biomass can be decomposed, and growth rates can be measured. However, the assumption is far less tenable for the cells and tissues of complex multicellular organisms, particularly if any integrated data is sampled from a heterogeneous collection of developing cells continually interacting between and across tissues. These will likely exhibit transient metabolic states equilibrating over varying timescales, and many FBA studies in complex organisms typically either ignore time as a parameter, or integrate data taken over long timescales (days/weeks). In this work, we adopt and modify a previously published machine learning approach originally developed to hybridize several aspects of a constraint-based approach with machine-learning in order to predict growth. This approach accommodates transient state dynamics, at the cost of tolerating a controlled amount of slack in the steady-state assumption, in order to enable transcript-constrained flux estimation in plant tissues without optimizing a growth objective. For our case study, we reconstruct the metabolism of the plastid of Poplar and Sorghum, integrating data sampled from leaf tissue under varying levels of iron bioavailability. The two species diverge sharply: Sorghum suppresses its photosynthetic electron transport and Calvin cycle abruptly at day 7 and its carbon delivery to biomass collapses to a third of control by day 21, whereas Poplar declines gradually and retains roughly 70%. Normalizing each reaction score to the plastid proteome pool makes the two species comparable and exposes reallocation as the pool contracts, including a split within Sorghums sulfate assimilation that tracks which enzymes carry iron cofactors.

bioinformatics↗

Biochemical characterisation of human transglutaminase 4

Transglutaminases are protein modifying enzymes involved in physiological and pathological processes with potent therapeutic possibilities. Human TG4, also called prostate transglutaminase, is frequently associated with pathological symptoms and particularly with cancer invasiveness. Although rodent TG4 is well characterised, bio-chemical characteristics of human TG4 that could help the understanding of its way of action are not published. First, we analysed proteomics databases and found that TG4 protein is present in human tissues beyond the prostate. Then, we studied in vitro the transamidase activity of human TG4 and its regulation using the microtiter plate method. Human TG4 has low transamidase activity which prefers slightly acidic pH and a reducing environment. It is enhanced by submicellar concentrations of SDS suggesting that membrane proximity is an important regulatory event. Human TG4 does not bind GTP as tested by GTP-agarose and BODIPY-FL-GTP{gamma}S binding, and its proteolytic activation by dispase or when expressed in AD-293 cells was not observed either. We identified several potential human TG4 glutamine donor substrates in the AD-293 cell extract by biotin-pentylamine incorporation and mass spectrometry. Several of these potential substrates are involved in cell-cell interaction, adhesion and proliferation, suggesting that human TG4 could become an anticancer therapeutic target.

biochemistry↗