ABCC7 p.Thr339Val

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PMID: 11557589 [PubMed] McCarty NA et al: "Identification of a region of strong discrimination in the pore of CFTR."
No. Sentence Comment
397 T339V CFTR, which did express in CHO cells, exhibited limited alterations in selectivity compared with mutants at T338 (24), consistent with a non-pore lining role for T339.
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ABCC7 p.Thr339Val 11557589:397:0
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PMID: 12745925 [PubMed] Gupta J et al: "Extent of the selectivity filter conferred by the sixth transmembrane region in the CFTR chloride channel pore."
No. Sentence Comment
41 Example leak-subtracted I Á/V relationships obtained with different intracellular anions are shown for wild-type, R334C, F337A, T338A, T339V and S341A in Figure 2.
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ABCC7 p.Thr339Val 12745925:41:140
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43 Other mutants studied (K335A, I336A, I340A), like T339V, had only minor effects (data not shown).
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ABCC7 p.Thr339Val 12745925:43:50
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44 Of eight mutants studied, only T339V was without any significant effect on anion permeability (Table 1), and five mutations (R334C, K335A, F337A, T338A, I340A) led to changes in the permeability sequence among halides (Figure 2 and Table 2).
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ABCC7 p.Thr339Val 12745925:44:31
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59 Wild type R334C K335A I336A F337A T338A T339V I340A S341A Cl 1.009/0.00 (6) 1.009/0.01 (6) 1.009/0.05 (5) 1.009/0.01 (5) 1.009/0.02 (6) 1.009/0.02 (8) 1.009/0.03 (6) 1.009/0.02 (5) 1.009/0.01 (6) Br 1.479/0.06 (6) 0.969/0.00 (5)** 1.529/0.03 (5) 1.359/0.05 (5) 0.669/0.03 (6)** 2.209/0.05 (5)** 1.829/0.24 (5) 1.409/0.09 (6) 2.459/0.20 (5)** I 0.819/0.04 (6) 0.729/0.05 (3) 1.579/0.06 (4)** 0.589/0.02 (4)* 0.389/0.15 (3)* 2.799/0.26 (7)** 0.769/0.02 (6) 1.249/0.07 (6)** 0.739/0.06 (6) F 0.119/0.01 (6) 0.099/0.01 (3) 0.139/0.02 (3) 0.079/0.01 (5) 0.409/0.02 (4)** 0.139/0.01 (6) 0.079/0.00 (5) 0.069/0.01 (5) 0.059/0.01 (6)* SCN 4.759/0.30 (6) 2.769/0.38 (6)** 3.989/0.16 (5) 3.709/0.11 (5)* 1.269/0.12 (5)** 7.509/0.29 (6)** 4.829/0.40 (5) 4.189/0.14 (7)* 10.09/1.8 (6)* Relative permeabilities for different anions present in the intracellular solution under bi-ionic conditions were calculated from macroscopic current reversal potentials according to Eq. (1) (see Experimental procedures).
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ABCC7 p.Thr339Val 12745925:59:40
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65 Wild-type R334C K335A I336A F337A T338A T339V I340A S341A Cl (G(50/G'50) 1.039/0.09 (6) 4.509/0.60 (6)** 1.399/0.09 (5)** 1.519/0.14 (5)* 1.189/0.22 (6) 1.779/0.25 (8)* 1.199/0.06 (7)* 1.419/0.11 (5)* 1.809/0.18 (5)** Cl (GCl/GCl) 1.009/0.08 (6) 1.009/0.13 (6) 1.009/0.07 (5) 1.009/0.09 (5) 1.009/0.22 (6) 1.009/0.14 (8) 1.009/0.06 (7) 1.009/0.09 (5) 1.009/0.10 (5) Br 0.649/0.05 (6) 0.329/0.02 (6)** 0.669/0.05 (5) 1.079/0.10 (5)* 0.359/0.06 (6)** 0.499/0.03 (5) 0.659/0.09 (5) 0.669/0.08 (6) 1.529/0.30 (4)* I 0.299/0.05 (6) 0.749/0.02 (3)* 0.279/0.01 (4) 0.109/0.02 (4)* 0.349/0.08 (3) 0.389/0.03 (5) 0.309/0.05 (7) 0.279/0.03 (6) 1.049/0.16 (7)** F 0.379/0.04 (6) 0.329/0.04 (3) 0.349/0.03 (3) 0.709/0.10 (4)* 0.129/0.02 (3)* 0.239/0.02 (6)* 0.509/0.10 (4) 0.309/0.02 (5) 0.519/0.07 (6) SCN 0.389/0.02 (6) 0.339/0.03 (6) 0.669/0.10 (5)* 0.279/0.02 (6)* 0.399/0.04 (5) 0.269/0.02 (5)* 0.269/0.02 (4)* 0.359/0.04 (6) 0.839/0.14 (6)* Relative conductances for different anions were calculated from the slope of the macroscopic I Á/V relationship for inward versus outward currents (see Experimental procedures).
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ABCC7 p.Thr339Val 12745925:65:40
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86 Halide permeability sequence Eisenman sequence CFTR variants I( !/Br( !/Cl( !/F( I K335A, T338A Br( !/I( !/Cl( !/F( II I340A Br( !/Cl( !/I( !/F( III wild-type, I336A, T339V, S341A Cl( !/Br( !/I( !/F( IV R334C Cl( !/Br( !/F( !/I( V F337A Sequences were derived from the relative permeabilities given in table 1.
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ABCC7 p.Thr339Val 12745925:86:167
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124 In most (six of eight) cases, alanine substitution was employed; however, we have previously found that the mutants R334A [15] and T339A [22] fail to express in BHK cells, and for these residues mutants which gave adequate current expression (R334C, T339V) were studied.
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ABCC7 p.Thr339Val 12745925:124:250
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PMID: 9729613 [PubMed] Linsdell P et al: "Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl- channel expressed in mammalian cell lines."
No. Sentence Comment
20 One mutant, T339V, was characterized in detail; its permeation properties were significantly altered, although these effects were not as strong as for T338 mutations.
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ABCC7 p.Thr339Val 9729613:20:12
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60 In contrast, of five mutations made at T339, only one (T339V) produced detectable levels of CFTR protein in Western blots using cell lysates from one confluent 10 cm culture plate (approximately 2 ² 10É-3 ² 10É cells; Fig. 1D).
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ABCC7 p.Thr339Val 9729613:60:55
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142 Permeability of intracellular anions in wild-type and mutant CFTR Cl¦ channels ------------------------------------------------------------ Anion WT T338A T338S T338N T338V T339V ------------------------------------------------------------ Thiocyanate 2·63 ± 0·13 (6) 5·85 ± 0·27 (4)* 4·80 ± 0·19 (3)* 8·72 ± 1·03 (4)* 1·92 ± 0·35 (4)* 3·28 ± 0·08 (4)* Nitrate 1·53 ± 0·04 (7) 2·04 ± 0·08 (3)* 1·82 ± 0·03 (4)* 4·22 ± 0·22 (3)* 6·84 ± 1·18 (7)* 1·61 ± 0·02 (3) Bromide 1·23 ± 0·03 (5) 1·74 ± 0·04 (3)* 1·47 ± 0·07 (3)* 1·66 ± 0·15 (3)* 1·04 ± 0·09 (5) 1·39 ± 0·06 (4)* Chloride 1·00 ± 0·01 (10) 1·00 ± 0·02 (11) 1·00 ± 0·02 (6) 1·00 ± 0·03 (10) 1·00 ± 0·04 (11) 1·00 ± 0·06 (10) Iodide 0·84 ± 0·03 (5) 2·09 ± 0·16 (5)* 1·76 ± 0·09 (3)* 1·03 ± 0·05 (3)* 0·79 ± 0·11 (3) 0·84 ± 0·02 (3) Perchlorate 0·25 ± 0·02 (6) 1·35 ± 0·08 (3)* 0·66 ± 0·06 (3)* 0·41 ± 0·03 (3)* 0·54 ± 0·00 (3)* 0·24 ± 0·01 (4) Benzoate 0·069 ± 0·006 (6) 0·17 ± 0·03 (4)* 0·091 ± 0·019 (3) 0·089 ± 0·015 (4) 0·15 ± 0·02 (4)* 0·097 ± 0·014 (4) Hexafluorophosphate < 0·019 (4) 0·53 ± 0·01 (3)* 0·31 ± 0·02 (3)* 0·68 ± 0·02 (3)* 0·39 ± 0·05 (3)* 0·051 ± 0·010 (4)* Fluoride 0·11 ± 0·01 (7) 0·12 ± 0·02 (4) 0·095 ± 0·012 (4) 0·11 ± 0·01 (4) 0·093 ± 0·009 (3) 0·17 ± 0·02 (4)* Formate 0·25 ± 0·01 (8) 0·45 ± 0·04 (3)* 0·43 ± 0·03 (3)* 0·35 ± 0·04 (4)* 0·22 ± 0·01 (3) 0·28 ± 0·02 (3) Acetate 0·090 ± 0·004 (8) 0·19 ± 0·01 (3)* 0·18 ± 0·01 (3)* 0·10 ± 0·02 (5) 0·11 ± 0·02 (3) 0·16 ± 0·01 (3)* Propanoate 0·14 ± 0·01 (3) 0·18 ± 0·02 (4) 0·098 ± 0·010 (4)* 0·077 ± 0·013 (3)* 0·13 ± 0·02 (3) - Pyruvate 0·10 ± 0·01 (5) 0·20 ± 0·01 (3)* 0·13 ± 0·02 (3) 0·075 ± 0·015 (3) 0·17 ± 0·03 (3)* - Methane sulphonate 0·077 ± 0·005 (5) 0·14 ± 0·02 (4)* 0·079 ± 0·014 (3) 0·038 ± 0·004 (3)* 0·088 ± 0·007 (3) - Glutamate 0·096 ± 0·008 (4) 0·082 ± 0·009 (3) 0·080 ± 0·008 (3) 0·060 ± 0·012 (5)* 0·11 ± 0·01 (3) - Isethionate 0·13 ± 0·01 (4) 0·11 ± 0·01 (3) 0·086 ± 0·012 (5)* 0·043 ± 0·007 (3)* 0·067 ± 0·005 (3)* - Gluconate 0·068 ± 0·004 (36) 0·10 ± 0·01 (3)* 0·060 ± 0·004 (3) 0·044 ± 0·004 (3) 0·077 ± 0·009 (3) 0·088 ± 0·021 (5) ------------------------------------------------------------ Relative permeabilities of different anions present in the intracellular solution under biionic conditions were calculated from macroscopic current reversal potentials (e.g. Figs 7 and 10) as described in Methods.
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ABCC7 p.Thr339Val 9729613:142:178
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173 Effects of mutations at T339 Of five amino acid substitutions carried out at position 339, only one (T339V) resulted in the production of detectable amounts of CFTR protein (Fig. 1D).
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ABCC7 p.Thr339Val 9729613:173:101
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175 PKAand ATP-dependent currents were observed, however, in twelve of fourteen T339V CFTR patches under the same conditions (Fig. 10A).
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ABCC7 p.Thr339Val 9729613:175:76
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176 T339V showed slight inward current rectification under these symmetrical ionic conditions (-I+50ÏI-50 = 0·86 ± 0·01; n = 8).
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ABCC7 p.Thr339Val 9729613:176:0
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178 Mean chord conductances for T339V were 7·95 ± 0·16 pS (n = 4) at -50 mV and 6·37 ± 0·29 pS (n = 3) at +50 mV, compared with wild-type values of 7·91 ± 0·09 pS (n = 18) at -50 mV and 7·85 ± 0·09 pS (n = 12) at +50 mV.
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ABCC7 p.Thr339Val 9729613:178:28
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179 As with T338A and T338S, T339V showed apparently normal channel gating, with open probability being time and P. Linsdell, S.-X. Zheng and J. W. Hanrahan J. Physiol. 512.110 Figure 9.
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ABCC7 p.Thr339Val 9729613:179:25
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183 Furthermore, as with T338 mutants, T339V had negligible cation permeability (data not shown).
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ABCC7 p.Thr339Val 9729613:183:35
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184 The T339V mutant also had significant alterations in ionic permeability (Fig. 10B and Table 1), although in general these were not as strong as those observed for T338 mutants.
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ABCC7 p.Thr339Val 9729613:184:4
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185 Indeed, the selectivity sequence for T339V (SCN¦ > NOצ > Br¦ > Cl¦ > I¦ > ClOÚ¦ > formate > F¦ > PFܦ) was the same as for wild-type (see Table 2).
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ABCC7 p.Thr339Val 9729613:185:37
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186 Gluconate permeability was not significantly altered in T339V, again suggesting no severe disruption of large organic anion permeability.
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ABCC7 p.Thr339Val 9729613:186:56
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187 All of these effects are consistent with the T339V mutant having less severely altered pore properties than any of the T338 mutants studied.
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ABCC7 p.Thr339Val 9729613:187:45
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197 Macroscopic current-voltage relationships for T339V CFTR A, T339V shows slight inward rectification with symmetrical Cl¦-containing solutions.
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ABCC7 p.Thr339Val 9729613:197:46
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ABCC7 p.Thr339Val 9729613:197:60
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198 B, example current-voltage relationships used to investigate the anion selectivity of T339V, measured under biionic conditions with ClOڦ or NOצ in the intracellular solution.
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ABCC7 p.Thr339Val 9729613:198:86
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199 Note that the permeability of these ions in T339V is similar to that observed in wild-type (Fig. 7).
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ABCC7 p.Thr339Val 9729613:199:44
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209 Inward rectification is observed in several other TM6 mutants at the single channel level, e.g. K335E (Tabcharani et al. 1993), T339V (Fig. 11B) and I332K (P. Linsdell, J. A. Tabcharani & J. W. Hanrahan, unpublished observations); however, voltage-dependent gating in T338 mutants cannot be excluded.
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ABCC7 p.Thr339Val 9729613:209:128
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222 Unitary properties of T339V CFTR A, activity of a single T339V channel at -50 mV (cf.
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ABCC7 p.Thr339Val 9729613:222:22
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ABCC7 p.Thr339Val 9729613:222:57
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224 B, mean single channel current-voltage relationships for wild-type (as in Fig. 4B and C) and T339V.
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ABCC7 p.Thr339Val 9729613:224:93
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237 However, it is unclear why mutations at T339 should apparently be more sensitive to misprocessing than those at T338 (Fig. 1C and D), or why the non-conservative T339V mutation alone should be appropriately processed (Fig. 1D).
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ABCC7 p.Thr339Val 9729613:237:162
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240 Because of low protein expression, we were only able to characterize the permeation properties of one T339 mutant, T339V.
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ABCC7 p.Thr339Val 9729613:240:115
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