Abstract

Molecular cloning and expression studies established the existence of three T-type Ca(2+) channel (Ca(v)3) alpha(1) subunits: Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I)). Although all three channels are low voltage-activated, they display considerable differences in their kinetics, with Ca(v)3.1 and Ca(v)3.2 channels activating and inactivating much faster than Ca(v)3.3 channels. The goal of the present study was to determine the structural elements that confer the distinctively slow kinetics of Ca(v)3.3 channels. To address this question, a series of chimeric channels between Ca(v)3.1 and Ca(v)3.3 channels were constructed and expressed in Xenopus oocytes. Kinetic analysis showed that the slow activation and inactivation kinetics of the Ca(v)3.3 channel were not completely abolished by substitution with any one portion of the Ca(v)3.1 channel. Likewise, the Ca(v)3.1 channel failed to acquire the slow kinetics by simply adopting one portion of the Ca(v)3.3 channel. These findings suggest that multiple structural elements contribute to the slow kinetics of Ca(v)3.3 channels.

Highlights

  • Relative currents were fit with the Boltzmann equation to determine the midpoint of voltage dependence

  • from double exponential fits to the current traces measured during test pulse to Ϫ20 mV. The data are shown with the means

  • the number of oocytes tested appears in parentheses

Read more

Summary

EXPERIMENTAL PROCEDURES

The plasmids carrying chimeric cDNAs are composed of the following sogang.ac.kr The plasmid pIG⌬C was constructed by ligating the above fragments with the AflII-digested (4701, ␣1I) and NotI-digested (3Јpolylinker) plasmid pcDNA3-I. The plasmid pIG⌬23L was constructed by ligating the above fragments with the KpnI-digested (5Ј-polylinker) and HindIII-digested (3651, ␣1I) plasmid pcDNA3-I. The plasmid pIG⌬12D was constructed by ligating these fragments with the KpnI-digested (5Ј-polylinker) and ClaI-digested (3901, ␣1I) plasmid pcDNA3-I. The plasmid pIG⌬34D was constructed by ligating the above fragments with KpnI-digested (5Ј-polylinker) and NotI-digested (3Ј-polylinker) plasmid pcDNA3-I. The plasmid pIG⌬234D was constructed by ligating the above fragments with the KpnI-digested (5Ј-polylinker) and BamHI-digested (7137, ␣1G) plasmid pcDNA3-G. The plasmid pIG⌬4D was constructed by ligating these fragments with the KpnI-digested (5Ј-polylinker) and AflII-digested (3Ј-polylinker) plasmid pGEMHEA-G.

Several ovary lobes were surgically removed from mature female
Electrophysiological Recordings in Oocytes and Data Analysis
RESULTS
DISCUSSION
TABLE I
Activation k
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call