Table 4. Changes in HV1 properties in S2 (134–156) and S2–S3 linker (157–165) mutants versus WT channels .
Mutant | Species | Expr. system | I? | τ act | τ tail | ΔV thr | ΔpH slope | Selectivity | Other | Reference |
---|---|---|---|---|---|---|---|---|---|---|
Y134A | hHV1 | HEK wc | Yes | 3 | Ramsey et al., 2010 | |||||
H140A | hHV1 | HEK wc | Yes | H+ | 9 × Kda Zn2+ | Ramsey et al., 2006 | ||||
H140A | hHV1 | Vesicle flux | nc H+ flux | Letts, 2014 | ||||||
H193A | hHV1 | HEK wc | Yes | H+ | 39 × Kda Zn2+ | Ramsey et al., 2006 | ||||
H140A/ H193A | hHV1 | HEK wc | Yes | −12 | 46 | H+ | 2,000 × Kda Zn2+ | Ramsey et al., 2006 | ||
H140A/ H193A | hHV1 | COS/HEK wc | Yes | H+ | Musset et al., 2011 | |||||
Y141A | hHV1 | HEK wc | Yes | −27 | Ramsey et al., 2010 | |||||
S143A | hHV1 | HEK wc | Yes | 11 | 41 | Ramsey et al., 2010 | ||||
S143A | hHV1 | Vesicle flux | nc H+ flux | Letts, 2014 | ||||||
D112V/S143D | hHV1 | COS/HEK wc | Yes | Cl– | Morgan et al., 2013 | |||||
D112V/I146D | hHV1 | COS/HEK wc | No | Morgan et al., 2013 | ||||||
D112V/L147D | hHV1 | COS/HEK wc | No | Morgan et al., 2013 | ||||||
F150A | hHV1 | Xenopus i-o | Yes | −24 | Hong et al., 2013 | |||||
F150C | hHV1 | Xenopus i-o | Yes | −22 | Hong et al., 2013 | |||||
F150W | hHV1 | Xenopus i-o | Yes | −55 | Hong et al., 2013 | |||||
E153A | hHV1 | HEK wc | Yes | −55 | 42 | Ramsey et al., 2010 | ||||
E153A | CiHV1 [E201A] | Xenopus TEVC | No | Chamberlin et al., 2014 | ||||||
E153G | CiHV1 [E201G] | Xenopus TEVC | No | Chamberlin et al., 2014 | ||||||
E153N | hHV1 | HEK wc | Yes | −1.17 | 45 | Ramsey et al., 2010 | ||||
E153A | hHV1 | Vesicle flux | nc H+ flux | Letts, 2014 | ||||||
E153D | hHV1 | HEK wc | Yes | −23 | 37 | Ramsey et al., 2010 | ||||
E153D/D174E | hHV1 | HEK wc | Yes | −102 | 40 | Ramsey et al., 2010 | ||||
E153C | hHV1 | Xenopus i-o | Yes | −55 | Tombola et al., 2010 | |||||
E153C | CiHV1 [E201C] | Xenopus TEVC | Yes | −101 | Chamberlin et al., 2014 | |||||
E153C/R205C | CiHV1 [E201C/R255C] | Xenopus TEVC | Yes | −43 | Chamberlin et al., 2014 | |||||
E153C/R208 | CiHV1 [E201C/R258C] | Xenopus TEVC | Yes | 37 | Chamberlin et al., 2014 | |||||
E153C/R211C | CiHV1 [E201CR261C] | Xenopus TEVC | Yes | −60 | Chamberlin et al., 2014 | |||||
K157A | hHV1 | HEK wc | Yes | 1 | 39 | Ramsey et al., 2010 | ||||
K157A | hHV1 | Vesicle flux | nc H+ flux | Letts, 2014 | ||||||
R162A | hHV1 | HEK wc | Yes | 13 | Ramsey et al., 2010 |
That numerical entries are shown does not imply that any given change was significant. Italicized mutant entries from nonhuman species show the hHV1 equivalent. HEK, HEK-293, HEK-293T, tsA, or HM1; COS, COS-7; Xenopus, Xenopus laevis oocyte; wc, whole cell; i-o, inside-out patch configuration; TEVC, two-electrode voltage clamp. Blank entries indicate that the parameter was not examined. nc, measured, but no change. Parameters are given relative to WT in each study. For I?, yes means currents are detectable. The ΔVthreshold value is the change in absolute position of the gH–V relationship versus WT. The ΔpH slope is the slope in millivolts of the relationship between Vthreshold (or other parameters reflecting the absolute position of the gH–V relationship) and Vrev or EH (which are not identical; see section Table entries defined).
Nominal Kd values are nearly meaningless for Zn2+ inhibition of HV1 because its main effects are slowing activation and shifting the gH–V relationship positively (Cherny and DeCoursey, 1999). As demonstrated in the Appendix of DeCoursey et al. (2001a), the apparent Kd derived from the ratio IH(Zn2+)/IH can vary more than three orders of magnitude depending on the test potential selected. If all measurements are done the same way, relative Kd values have meaning.