Abstract
Excitatory amino acid transporter 1 plays an important role in keeping the synaptic glutamate concentration below neurotoxic levels by translocating this neurotransmitter into the cell. Both reentrant hairpin loops, HP1 and -2, have been shown to take part in binding the substrate and the more deeply buried sodium ion, and might therefore be a part of the intra- or extracellular gate of the transporter. However, the shape of the motion of either loop relative to transmembrane domain (TM) 4 during the transport cycle has not yet been fully resolved. Using copper(II) (1,10-phenanthroline)3 (CuPh) for cross-linking cysteine pairs, we found strong inhibition of transport when A243C (TM4) was combined with S366C (HP1), I453C (HP2), or T456C (HP2). These findings were reinforced by the impact of cadmium on transport activity, and both approaches consistently showed that proximity was exclusively intramonomeric. Under conditions that promote the inward-facing state, inhibition by CuPh in A243C/S366C was reduced, while the opposite was seen when the outward-facing one was stabilized, suggesting that the two positions are farther apart in the former conformation than in the latter. Surprisingly, maximal cross-linking of A243C with I453C or T456C was not observed under conditions that promote the inward-facing state. Altogether, our data suggest that the transporter may undergo complex relative movement between these positions on TM4 and HP1/HP2 during the transport cycle.
Footnotes
- Received July 26, 2014.
- Accepted September 29, 2014.
This work was supported by the National Natural Science Foundation of China [Grant 31170734], the International Centre for Genetic Engineering and Biotechnology [Grant CRP/CHN11-01], the Specialized Research Fund for the Doctoral Program of Higher Education [Grant 20114433120002], and the Specialized Research Fund for talent introduction of colleges and universities of Guangdong Province [Grant 2011430-1]. The authors declare no competing financial interests.
- Copyright © 2014 by The American Society for Pharmacology and Experimental Therapeutics
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