Several models of prebiological systems are described and analyzed. The following models are characterized: a quasispecies model, a hypercycle model, a syser model (the term "syser" is an abbreviation of SYstem of SElf-Reproduction), a stochastic corrector model, a model of the origin of a primordial genome through spontaneous symmetry breaking. The quasispecies model analyzes the Darwinian evolution of information chains; this evolution is similar to the evolution of RNA molecules. Rather general estimates of the speed and efficiency of evolutionary processes can be obtained in the framework of the quasispecies model. We briefly describe the method for obtaining these estimates and the corresponding results. The hypercycle model considers the interaction of RNA chains and enzymes. The syser model characterizes a rather general scheme of the self-reproducing system, which is similar to the self-reproducing systems of biological cells. Syser includes a polynucleotide sequence, a replication enzyme, a translation enzyme, and other enzymes; these macromolecules are located inside the protocell. The stochastic corrector model describes the process of using a relatively small number of molecules of competing and cooperating replicators in protocells. The model of the origin of a primordial genome through spontaneous symmetry breaking characterizes an interesting and important process of the appearance of genotypes in protocells. This model was proposed and investigated by Takeuchi, Hogeweg, and Kaneko in 2017; we call it further “the THK model.” The current article characterizes and compares all these models. 相似文献
The article describes a colorimetric assay for the determination of thrombin. It is based on the application of a triple enzyme-mimetic activity and a dual aptamer binding strategy. The triple signal amplification relies on oxidation of the chromogenic enzyme substrate 3,3,5,5-tetramethylbenzidine (TMB) that is catalyzed by composites consisting of graphene oxide (GO), gold/platinum nanoparticles (AuPtNP), and aptamer (Apt15), a G-quadruplex/hemin conjugate. The dual-aptamer target binding strategy is based on the fact that thrombin has two active sites to be recognized by its aptamers (Apt15 and Apt29). Magnetic beads (MBs) were modified with Apt29 (Apt29-MB) and then are bound by the GO-AuPtNP-Apt15/G-quadruplex/hemin composites. In the presence of thrombin, Apt29-MB and the GO-AuPtNP-Apt15/G-quadruplex/hemin composites form a sandwich-like superstructure. Thus, the absorbance increases due to the formation of TMB oxide produced by catalysis of the composites. Under optimized conditions, the absorbance at 450 nm increases linearly in the 0.30 to 100 nM thrombin concentration range, and the limit of detection is 0.15 nM. The method is simple, rapid, and does not require complicated instrumentation. Bovine serum albumin, human serum albumin and other proteins were found not to interfere.
Graphical abstract Schematic presentation of the photometric thrombin assay based on a triple enzyme-mimetic activity of combined nanomaterials (consisting of GO, AuPtNPs and the G-quadruplex/hemin DNAzyme) and two aptamers TMB: 3,3,5,5-tetramethylbenzidine, TMBox: 3,3,5,5-tetramethylbenzidine oxide, AuPtNP: gold/platinum nanoparticles).
An approximate critical explosion parameter, which separates the slow and explosive reactions is determined with respect to
the initial data, using the asymptotic technique to analyze a one step reaction mechanism with temperature dependent pre-exponential
factor. We obtained and analysed the effect of the variable pre-exponential factor on the critical temperature, critical parameter
for thermal explosion and the first order approximation of the slow curve. By introducing a new coordinate and using the Method
of Invariant Manifold (MIM), we obtained corrections on the critical temperature. The results obtained are not only general;
they also reveal some salient properties of the system hitherto unknown. 相似文献
