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1.
FEBS Lett ; 579(23): 5187-92, 2005 Sep 26.
Artículo en Inglés | MEDLINE | ID: mdl-16150446

RESUMEN

Reconstitution into planar lipid bilayers of a poly-3-hydroxybutyrate/calcium/polyphosphate (PHB/Ca(2+)/polyP) complex from Escherichia coli membranes yields cationic-selective, 100 pS channels (Das, S., Lengweiler, U.D., Seebach, D. and Reusch, R.N. (1997) Proof for a non-proteinaceous calcium-selective channel in Escherichia coli by total synthesis from (R)-3-hydroxybutanoic acid and inorganic polyphosphate. Proc. Natl. Acad. Sci. USA 94, 9075-9079). Here, we report that this complex can also form larger, weakly selective pores, with a maximal conductance ranging from 250pS to 1nS in different experiments (symmetric 150mM KCl). Single channels were inhibited by lanthanum (IC(50)=42+/-4microM, means+/-S.E.M.) with an unusually high Hill coefficient (8.4+/-1.2). Transition to low-conductance states (<250pS) was favored by increased membrane polarization (/V/ >or=50mV). High conductance states (>250pS) may reflect conformations important for genetic transformability, or "competence", of the bacterial cells, which requires the presence of the PHB/Ca(2+)/polyP complex in the membrane.


Asunto(s)
Canales de Calcio/metabolismo , Calcio/metabolismo , Proteínas de Escherichia coli/metabolismo , Escherichia coli/metabolismo , Hidroxibutiratos/metabolismo , Poliésteres/metabolismo , Polifosfatos/metabolismo , Escherichia coli/genética , Activación del Canal Iónico , Lantano/metabolismo , Membrana Dobles de Lípidos , Potenciales de la Membrana , Complejos Multiproteicos , Técnicas de Placa-Clamp , Polifosfatos/química
2.
Biophys J ; 88(4): 2614-25, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15695627

RESUMEN

We examined ion channels derived from a chloroform extract of isolated, dehydrated rat liver mitochondria. The extraction method was previously used to isolate a channel-forming complex containing poly-3-hydroxybutyrate and calcium polyphosphate from Escherichia coli. This complex is also present in eukaryotic membranes, and is located primarily in mitochondria. Reconstituted channels showed multiple subconductance levels and were voltage-dependent, showing an increased probability of higher conductance states at voltages near zero. In symmetric 150 mM KCl, the maximal conductance of the channel ranged from 350 pS to 750 pS. For voltages >+/-60 mV, conductance fluctuated in the range of approximately 50- approximately 200 pS. In the presence of a 1:3 gradient of KCl, at pH = 7.4, selectivity periodically switched between different states ranging from weakly anion-selective (V(rev) approximately -15 mV) to ideally cation-selective (V(rev) approximately +29 mV), without a significant change in its conductance. Overall, the diverse, but highly reproducible, channel activity most closely resembled the behavior of the permeability transition pore channel seen in patch-clamp experiments on native mitoplasts. We suggest that the isolated complex may represent the ion-conducting module from the permeability transition pore.


Asunto(s)
Biofisica/métodos , Cloroformo/farmacología , Mitocondrias Hepáticas/metabolismo , Mitocondrias/metabolismo , Porinas/aislamiento & purificación , Animales , Cationes , Cloroformo/química , Cromatografía , Ciclosporina/farmacología , Electroforesis en Gel de Poliacrilamida , Electrofisiología , Escherichia coli/metabolismo , Concentración de Iones de Hidrógeno , Hidroxibutiratos/farmacología , Iones , Lantano/farmacología , Membrana Dobles de Lípidos/metabolismo , ATPasas de Translocación de Protón Mitocondriales/química , Permeabilidad , Poliésteres/farmacología , Cloruro de Potasio/química , Ratas , Ratas Sprague-Dawley , Canales Aniónicos Dependientes del Voltaje , Agua/química
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