CPL - Chalmers Publication Library
| Utbildning | Forskning | Styrkeområden | Om Chalmers | In English In English Ej inloggad.

Controlling desensitized states in ligand-receptor interaction studies with cyclic scanning patch-clamp Protocols

D. Granfeldt ; J. Sinclair ; Maria Millingen (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; C. Farre ; Per Lincoln (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; Owe Orwar (Institutionen för kemi- och bioteknik, Fysikalisk kemi)
Analytical Chemistry (0003-2700). Vol. 78 (2006), 23, p. 7947-7953.
[Artikel, refereegranskad vetenskaplig]

Ligand-gated ion channels are important control elements in regulation of cellular activities, and increasing evidence demonstrates their role as therapeutic targets. The receptors display complex desensitization kinetics, occurring on vastly different time scales. This is not only important in biology and pharmacology but might also be of technological significance since populations of receptors under microfluidic control can function analogously to DRAM memory circuits. Using a novel microfluidic method, and computer modeling of the receptor state distributions, we here demonstrate that GABA(A) receptor populations can be controlled to display high or low EC50 values, depending on input function (i.e., the exact pattern of agonist application). The sensitivity of the receptors can be tuned up to 40-fold (beta-alanine) by the particular agonist exposure pattern. By combining patch-clamp experiments with computer modeling of receptor state distributions, we can control the assembly of receptors in desensitized states. The technique described can be used as an analytical tool to study the effect of desensitization on the activity of ion channel effectors. We describe the differential blocking effect of the competitive antagonist bicuculline on the high- and low-EC50 GABA(A) receptor preparations and conclude that the inhibition is dramatically dependent on how the different desensitized states are populated. Furthermore, we show that both GABA and beta-alanine, two agonists with different affinity but similar efficacy, induce the same type of desensitization behavior and memory effects in GABA(A) receptors.



Denna post skapades 2007-02-05. Senast ändrad 2009-02-19.
CPL Pubid: 26229

 

Läs direkt!


Länk till annan sajt (kan kräva inloggning)


Institutioner (Chalmers)

Institutionen för kemi- och bioteknik, Fysikalisk kemi (2005-2014)

Ämnesområden

Kemi

Chalmers infrastruktur

Relaterade publikationer

Denna publikation ingår i:


Patch-clamp studies of the GABAA receptor using microfluidic methods


Studies of ligand- and temperature-gated ion channels using microfluidic methods