ABCB1 p.Tyr401Cys
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PMID: 16768456
[PubMed]
Kim IW et al: "The conserved tyrosine residues 401 and 1044 in ATP sites of human P-glycoprotein are critical for ATP binding and hydrolysis: evidence for a conserved subdomain, the A-loop in the ATP-binding cassette."
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86
HighFive insect cells (Invitrogen) were infected with the recombinant baculovirus carrying the wild type and Y401A, Y1044A, Y401A/Y1044A, Y401C, Y401L, and Y401W mutant human MDR1 cDNAs with a His6 tag at the C-terminal end [BV-MDR1(His6)] as described previously (37).
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ABCB1 p.Tyr401Cys 16768456:86:138
status: NEW100 The Pgp‚Mg-8-azido[R-32 P]ADP‚ BeFx or Pgp‚Mg-8-azido[R-32 P]ADP‚Vi preor posthydrolysis transition state conformation was generated as described Table 1: Effect of Substitution of the Conserved Y401 and Y1044 Residues in ATP Sites on Pgp Cell Surface Expression, Transport Function, ATP Binding, Nucleotide Trapping, and Hydrolysisa construct cell surface expressionb (%) transport functionc (%) ATP bindingd (%) ADP-Vi trappinge (%) ATP hydrolysisf (%) wild-type MDR1 100 100 100 100 100 Y401W 100 100 90-95 90-95 85-90 Y401F 95-100 90-100 NTg NTg NTg Y401C 90-95 45-55 50 <20 NTg Y401L 95-100 25-30 30-35 20-25 NTg Y401A 100-110 <2 <15 <2 <2 Y1044W 100 100 NTg NTg NTg Y1044F 95-100 90-100 NTg NTg NTg Y1044C 90-95 <2 NTg NTg NTg Y1044A 100 <2 <5 <2 <2 Y401W/Y1044W 90-95 <2 NTg NTg NTg Y401F/Y1044F 90-95 95-100 NTg NTg NTg Y401C/Y1044C 100 <2 NTg NTg NTg Y401A/Y1044A 90-95 <2 <2 <2 <2 Y401F/Y1044W 100 100 NTg NTg NTg Y401C/Y1044W 100 <2 NTg NTg NTg Y401A/Y1044W 100-110 <2 NTg NTg NTg Y401W/Y1044F 100 100 NTg NTg NTg a The levels of cell surface expression, transport activity, ATP binding, nucleotide trapping, and ATP hydrolysis by the wild-type protein were taken to be 100%, and these activities in mutant Pgps were expressed relative to wild-type levels.
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ABCB1 p.Tyr401Cys 16768456:100:582
status: NEWX
ABCB1 p.Tyr401Cys 16768456:100:583
status: NEWX
ABCB1 p.Tyr401Cys 16768456:100:856
status: NEW144 We generated the single mutants Y401A, Y1044A, Y401C, Y1044C, Y401F, Y1044F, Y401W, Y1044W, and Y401L.
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ABCB1 p.Tyr401Cys 16768456:144:47
status: NEW145 We also generated the double mutants Y401A/Y1044A, Y401F/Y1044F, Y401W/Y1044W, Y401C/Y1044C, Y401A/Y1044W, Y401F/Y1044W, Y401C/ Y1044W, and Y401W/Y1044F.
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ABCB1 p.Tyr401Cys 16768456:145:79
status: NEWX
ABCB1 p.Tyr401Cys 16768456:145:121
status: NEW153 Figure 2 illustrates that in a flow cytometry assay HeLa cells expressing wild-type Pgp show a reduced level of accumulation of fluorescent calcein, whereas cells expressing equivalent amounts of Y401L and Y401C mutant Pgps show partial (30-50%) transport function (Table 1).
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ABCB1 p.Tyr401Cys 16768456:153:206
status: NEW159 Furthermore, it would be expected that the substitution of both Y401 and Y1044 with A and C (Y401A/Y1044A and Y401C/Y1044C) would abrogate function, whereas substitutions with F and W in both NBDs (Y401F/Y1044F and Y401W/Y1044W) would retain functionality.
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ABCB1 p.Tyr401Cys 16768456:159:110
status: NEW161 We also found loss of function in mutants Y401A/ Y1044W and Y401C/Y1044W.
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ABCB1 p.Tyr401Cys 16768456:161:60
status: NEW163 The cell surface expression of wild-type and mutant Pgps was assessed by staining Pgp in intact cells with human Pgp-specific monoclonal antibody MRK-16 (33) followed by flow cytometry as described in Experimental Procedures: (A) (thin line) pTM1, (thick line) wild type, (‚‚‚) Y401A, (- - -) Y401C, (-‚-) Y401W, and (-‚‚-) Y401F, (B) (thin line) pTM1, (thick line) wild type, (‚‚‚) Y1044A, (- - -) Y1044C, (-‚-) Y1044W, and (-‚‚-) Y1044F, and (C) (thin line) pTM1, (thick line) wild type, (‚‚‚) Y401A/Y1044A, (- - -) Y401C/Y1044C, (-‚-) Y401W/ Y1044W, and (-‚‚-) Y401F/Y1044F.
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ABCB1 p.Tyr401Cys 16768456:163:314
status: NEWX
ABCB1 p.Tyr401Cys 16768456:163:623
status: NEW169 Binding of 8-Azido[R-32 P]ATP to Wild-Type, Y401A, Y1044A, Y401A/Y1044A, Y401W, Y401C, and Y401L Mutant Pgps.
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ABCB1 p.Tyr401Cys 16768456:169:80
status: NEW175 In Y401L and Y401C mutants, 30-50% of the azidonucleotide was incorporated.
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ABCB1 p.Tyr401Cys 16768456:175:13
status: NEW200 cross-linking with 8-azidoATP at 4 °C, both Y401L and Y401C trap ~20% nucleotide in the presence of vanadate (Table 1).
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ABCB1 p.Tyr401Cys 16768456:200:59
status: NEW264 Similar results were also obtained with Y401L and Y401C mutants (see Table 1).
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ABCB1 p.Tyr401Cys 16768456:264:50
status: NEW265 The partial activity is observed only with Y401C in NBD1 and not with Y1044C in NBD2, suggesting that there might be cooperativity and slight asymmetry in NBD1 and NBD2.
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ABCB1 p.Tyr401Cys 16768456:265:43
status: NEW297 Consistent with this view is the fact that while mutants Y401L and Y401C are partially (30-50%) functional, mutants Y1044C and Y401C/Y1044C are completely nonfunctional (Table 1).
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ABCB1 p.Tyr401Cys 16768456:297:67
status: NEWX
ABCB1 p.Tyr401Cys 16768456:297:127
status: NEW308 On the other hand, in the Y401C mutant, the S group of the C residue interacts with C6 of the adenine base through hydrogen bonding (distance of 3.3 Å).
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ABCB1 p.Tyr401Cys 16768456:308:26
status: NEW
No.
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Comment
78
Y401C and Y401L mutant P-gps showed partial (30-50%) transport function.
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ABCB1 p.Tyr401Cys 18058211:78:0
status: NEW