Publications by authors named "Felix Olasagasti"

Research on mA-associated SNPs (mA-SNPs) has emerged recently due to their possible critical roles in many key biological processes. In this sense, several investigations have identified mA-SNPs in different diseases. In order to gain a more complete understanding of the role that mA-SNPs can play in breast cancer, we performed an analysis to identify the mA-SNPs associated with breast cancer and to evaluate their possible effects.

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In addition to being one of the proponents of the "Lipid World hypothesis", David Deamer, together with other colleagues, pioneered studies involving formation of RNA-like oligomers from their 'non-activated', prebiotically plausible monomeric moieties. In particular, the pioneering work in this regard was a publication from 2008 in , , wherein we described the formation of RNA-like oligomers from nucleoside 5'-monophosphates. In that study, we had simulated a terrestrial geothermal environment, a niche that is thought to have facilitated the prebiotic non-enzymatic synthesis of polynucleotides.

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The field of point-of-care (POC) testing technology is developing quickly and producing instruments that are increasingly reliable, while their size is being gradually reduced. Proteins are a common target for POC analyses and the detection of protein markers typically involves immunoassays aimed at detecting different groups of proteins such as tumor markers, inflammation proteins, and cardiac markers; but other techniques can also be used to analyze plasma proteins. In the case of nucleic acids, hybridization and amplification strategies can be used to record electromagnetic or electric signals.

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We simulated in our laboratory a prebiotic environment where dry and wet periods were cycled. Under anhydrous conditions, lipid molecules present in the medium could form fluid lamellar matrices and work as organizing agents for the condensation of nucleic acid monomers into polymers. We exposed a mixture of 2'-deoxyribonucleoside 5'-monophosphates and a ssDNA oligomer template to this dry environment at 90 °C under a continuous gentle stream of CO(2) and we followed it with rehydration periods.

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Article Synopsis
  • Coupling nucleic acid processing enzymes with nanoscale pores enables the controlled movement of DNA or RNA strands, which can be monitored through ionic current measurements over time.
  • The phi29 DNA polymerase is particularly effective for this method due to its strong binding to DNA and ability to replicate efficiently.
  • This study demonstrates the stability of phi29 DNAP-DNA complexes within the nanopore and allows for real-time observation of DNA synthesis and translocation at extremely precise measurements.
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Nanopores can be used to analyse DNA by monitoring ion currents as individual strands are captured and driven through the pore in single file by an applied voltage. Here, we show that serial replication of individual DNA templates can be achieved by DNA polymerases held at the α-haemolysin nanopore orifice. Replication is blocked in the bulk phase, and is initiated only after the DNA is captured by the nanopore.

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DNA polymerases are molecular motors that catalyze template-dependent DNA replication, advancing along template DNA by one nucleotide with each catalytic cycle. Nanopore-based measurements have emerged as a single molecule technique for the study of these enzymes. Using the alpha-hemolysin nanopore, we determined the position of DNA templates bearing inserts of abasic (1',2'-dideoxy) residues, bound to the Klenow fragment of Escherichia coli DNA polymerase I (KF) or to bacteriophage T7 DNA polymerase.

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This paper presents an extension of stoichiometric analysis in systems where the catalytic compounds (enzymes) are also intermediates of the metabolic network (dual property), so they are produced and degraded by the reaction network itself. To take this property into account, we introduce the definition of enzyme-maintaining mode, a set of reactions that produces its own catalyst and can operate at stationary state. Moreover, an enzyme-maintaining mode is defined as elementary with respect to a given reaction if the removal of any of the remaining reactions causes the cessation of any steady state flux through this reference reaction.

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A fundamental problem in research on the origin of life is the process by which polymers capable of catalysis and replication were produced on the early Earth. Here we show that RNA-like polymers can be synthesized non-enzymatically from mononucleotides in lipid environments. The RNA-like polymers were initially identified by nanopore analysis, a technique with single molecule sensitivity.

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Most of the models for cellular origin stress one of these two approaches: "replication-first" or "metabolism-first." The model presented here focuses on the latter, consisting of the combination of kinetic and energetic descriptions of protocellular metabolism. In this model, the membrane plays a very crucial role in the maintenance of the cell and the osmotic stability.

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