Biomedical subjects

Guillaume Legent

Publications and source records attributed to Guillaume Legent.

3 recordsLinked to original sources

PubMed2006

Steady-state kinetic behaviour of two- or n-enzyme systems made of free sequential enzymes involved in a metabolic pathway.

The overall rate of functioning of a set of free sequential enzymes of the Michaelis-Menten type involved in a metabolic pathway has been computed as a function of the concentration of the initial substrate under steady-state conditions. Curves monotonically increasing up to a saturation plateau have been obtained in all cases. The shape of these curves is sometimes, but not usually, close to that of a hyperbola. Cases exist in which the overall rate of reaction becomes quasi proportional to the concentration of initial substrate almost up to the saturation plateau, which never occurs with individual enzymes. Increasing the number of enzymes sequentially involved in a metabolic pathway does not seem to generate any particularly original behaviour compared with that of two-enzyme systems.

Enzymes↗

PubMed2006

Steady-state kinetic behaviour of functioning-dependent structures.

A fundamental problem in biochemistry is that of the nature of the coordination between and within metabolic and signalling pathways. It is conceivable that this coordination might be assured by what we term functioning-dependent structures (FDSs), namely those assemblies of proteins that associate with one another when performing tasks and that disassociate when no longer performing them. To investigate a role in coordination for FDSs, we have studied numerically the steady-state kinetics of a model system of two sequential monomeric enzymes, E(1) and E(2). Our calculations show that such FDSs can display kinetic properties that the individual enzymes cannot. These include the full range of basic input/output characteristics found in electronic circuits such as linearity, invariance, pulsing and switching. Hence, FDSs can generate kinetics that might regulate and coordinate metabolism and signalling. Finally, we suggest that the occurrence of terms representative of the assembly and disassembly of FDSs in the classical expression of the density of entropy production are characteristic of living systems.

Dimerization↗

PubMed2004

Introduction to the concept of functioning-dependent structures in living cells.

The assembly of proteins into larger structures may confer advantages such as increased resistance to hydrolytic enzymes. metabolite channelling, and reduction of the number of proteins or other active molecules required for cell functioning. We propose the term functioning-dependent structures (FDSs) for those associations of proteins that are created and maintained by their action in accomplishing a function, as reported in many experiments. Here we model the simplest possible cases of two-partner FDSs in which the associations either catalyse or inhibit reactions. We show that FDSs may display regulatory properties (e.g., a sigmoidal response or a linear kinetic behaviour over a large range of substrate concentrations) even when the individual proteins are enzymes of the Michaelis-Menten type. The possible involvement of more complicated FDSs or of FDS networks in real living systems is discussed. From the thermodynamic point of view, FDS formation and decay are responsible for an extra production of entropy, which may be considered characteristic of living systems.

Cell Physiological Phenomena↗