An enquiry into metabolite domains

Barros, LF; Martínez C

Abstract

It is currently assumed that two or more pools of the same metabolite can coexist in the cytosolic compartment of mammalian cells. These pools are thought to be generated by the differential subcellular location of enzymes and transporters, much in the way calcium microdomains arise by the combined workings of channels, buffers, and pumps. With the aim of estimating the amplitude and spatial dimensions of these metabolite pools, we developed an analytical tool based on Brownian diffusion and the turnover numbers of the proteins involved. The outcome of the analysis is that ATP, glucose, pyruvate, lactate, and glutamate cannot be concentrated at their sources to an extent that would affect their downstream targets. For these metabolites, and others produced by slow enzymes or transporters and present at micromolar concentrations or higher, the cytosol behaves as a well-mixed, homogenous compartment. In contrast, the analysis showed microdomains known to be generated by calcium channels and revealed that calcium and pH nanodomains are to be found in the vicinity of slow enzymes and transporters in the steady state. The analysis can be readily applied to any other molecule, provided knowledge is available about rate of production, average concentration, and diffusion coefficient. Our main conclusion is that the notion of cytosolic compartmentation of metabolites needs reevaluation, as it seems to be in conflict with the underlying physical chemistry. © 2007 by the Biophysical Society.

Más información

Título según WOS: An enquiry into metabolite domains
Título según SCOPUS: An enquiry into metabolite domains
Título de la Revista: BIOPHYSICAL JOURNAL
Volumen: 92
Número: 11
Editorial: Cell Press
Fecha de publicación: 2007
Página de inicio: 3878
Página final: 3884
Idioma: English
URL: http://linkinghub.elsevier.com/retrieve/pii/S0006349507711876
DOI:

10.1529/biophysj.106.100925

Notas: ISI, SCOPUS