ABCC1 p.Trp1246Phe

[switch to full view]
Comments [show]
Publications
PMID: 11278867 [PubMed] Ito K et al: "Mutation of a single conserved tryptophan in multidrug resistance protein 1 (MRP1/ABCC1) results in loss of drug resistance and selective loss of organic anion transport."
No. Sentence Comment
3 A similar phenotype was observed when Trp1246 was replaced with Ala, Phe, and Tyr.
X
ABCC1 p.Trp1246Phe 11278867:3:38
status: NEW
Login to comment

47 Mutagenesis was then performed according to the manufacturer`s instructions with the following sense mutagenic primers (substituted nucleotides are underlined): W1246C, 5Ј-CCACGTACT- TGAACTGCCTGGTTCGGATGTC-3Ј; W1246A, 5Ј-CCACGTACTTGAA- CGCGCTGGTTCGGATGTC-3Ј; W1246F, 5Ј-CCACGTACTTGAACTTC- CTGGTTCGGATGTC-3Ј; and W1246Y, 5Ј-CCACGTACTTGAACTATCT- GGTTCGGATGTC-3Ј.
X
ABCC1 p.Trp1246Phe 11278867:47:283
status: NEW
Login to comment

128 These included substitution with a nonpolar non-aromatic amino acid (Ala; W1246A-MRP1) as well as conservative substitutions with polar (Tyr; W1246Y-MRP1) and nonpolar (Phe; W1246F-MRP1) aromatic amino acids.
X
ABCC1 p.Trp1246Phe 11278867:128:174
status: NEW
Login to comment

131 The LTC4 transport levels of the W1246A-MRP1 mutant (Fig. 3B) and the W1246Y-MRP1 and W1246F-MRP1 mutants (Fig. 3C) were similar to those of wild-type MRP1 and the W1246C-MRP1 mutant.
X
ABCC1 p.Trp1246Phe 11278867:131:86
status: NEW
Login to comment

133 E217betaG transport by the W1246Y and W1246F mutants was also extremely low (ϳ10% of wild-type MRP1) (Fig. 3E).
X
ABCC1 p.Trp1246Phe 11278867:133:38
status: NEW
Login to comment

144 A, immunoblots of membrane vesicles prepared from HEK293T cells transiently transfected with pcDNA3.1(-)-MRP1K (wild-type MRP1 (WT-MRP1)), pcDNA3.1(-)-W1236A-MRP1, pcDNA3.1(-)-W1246C-MRP1, pcDNA3.1(-)-W1246F-MRP1, pcDNA3.1(-)-W1246Y-MRP1, and pcDNA3.1(-) alone as a control.
X
ABCC1 p.Trp1246Phe 11278867:144:201
status: NEW
Login to comment

146 B and C, time course of [3 H]LTC4 uptake by inside-out membrane vesicles prepared from HEK293T cells expressing MRP1 mutants W1246A (Ⅺ) and W1246C (f) (B) and W1246F (Œ) and W1246Y () (C).
X
ABCC1 p.Trp1246Phe 11278867:146:166
status: NEW
Login to comment

149 D and E, time course of [3 H]E217betaG uptake by inside-out membrane vesicles prepared from MRP1 mutants W1246A (Ⅺ) and W1246C (f) (D) and W1246F (Œ) and W1246Y () (E).
X
ABCC1 p.Trp1246Phe 11278867:149:146
status: NEW
Login to comment

PMID: 12034727 [PubMed] Mao Q et al: "GSH-dependent photolabeling of multidrug resistance protein MRP1 (ABCC1) by [125I]LY475776. Evidence of a major binding site in the COOH-proximal membrane spanning domain."
No. Sentence Comment
56 Cell Culture and Membrane Protein Preparation-The doxorubicin-selected, multidrug-resistant H69AR small cell lung cancer cell line that expresses high levels of MRP1, and the transfected HeLa cell lines that express recombinant wild-type MRP1 (T5 or WT-MRP1), and mutant MRP1 bearing substitutions of Trp1246 (W1246F-MRP1, W1246Y-MRP1, W1245C-MRP1, and W1246A-MRP1) were maintained as described previously (15, 37).
X
ABCC1 p.Trp1246Phe 12034727:56:310
status: NEW
Login to comment

154 After normalizing expression levels of the mutant MRP1 molecules relative to wild-type MRP1 (Fig. 8B), it was estimated that [125 I]LY475776 labeling of HeLa cell membrane proteins containing the W1246F-MRP1 mutant was ϳ23% of wild-type MRP1 membrane proteins, whereas labeling of membranes containing the W1246Y-MRP1, W1246C-MRP1, and W1246A-MRP1 mutants was less than 10% of wild-type MRP1 levels.
X
ABCC1 p.Trp1246Phe 12034727:154:196
status: NEW
Login to comment

163 Membrane vesicles (50 ␮g of protein) were prepared from stably transfected HeLa cells expressing wild-type (WT-MRP1) and mutant MRP1 molecules in which Trp1246 has been replaced with Ala (W1246A), Phe (W1246F), Cys (W1246C), or Tyr (W1246Y).
X
ABCC1 p.Trp1246Phe 12034727:163:209
status: NEW
Login to comment

PMID: 16816140 [PubMed] Deeley RG et al: "Transmembrane transport of endo- and xenobiotics by mammalian ATP-binding cassette multidrug resistance proteins."
No. Sentence Comment
798 For example, mutation of Trp1246 to Cys, Ala, Phe, or Tyr eliminated E217betaG and NNAL-O-glucuronide transport, resistance to natural product drugs, and binding of the GSH-dependent inhibitor LY475776, but had little effect or no effect on LTC4 transport (207, 281, 327).
X
ABCC1 p.Trp1246Phe 16816140:798:25
status: NEW
Login to comment

797 For example, mutation of Trp1246 to Cys, Ala, Phe, or Tyr eliminated E217betaG and NNAL-O-glucuronide transport, resistance to natural product drugs, and binding of the GSH-dependent inhibitor LY475776, but had little effect or no effect on LTC4 transport (207, 281, 327).
X
ABCC1 p.Trp1246Phe 16816140:797:25
status: NEW
Login to comment

799 For example, mutation of Trp1246 to Cys, Ala, Phe, or Tyr eliminated E217betaG and NNAL-O-glucuronide transport, resistance to natural product drugs, and binding of the GSH-dependent inhibitor LY475776, but had little effect or no effect on LTC4 transport (207, 281, 327).
X
ABCC1 p.Trp1246Phe 16816140:799:25
status: NEW
Login to comment

PMID: 17295059 [PubMed] Chang XB et al: "A molecular understanding of ATP-dependent solute transport by multidrug resistance-associated protein MRP1."
No. Sentence Comment
117 Many mutations in TM17, such as Y1236F, T1241A, T1242A, T1242C, T1242S, T1242L, Y1243F, N1245A, W1246C, W1246A, W1246F, W1246Y, or R1249K, significantly affect MRP1 function [83-86].
X
ABCC1 p.Trp1246Phe 17295059:117:112
status: NEW
Login to comment

PMID: 19398503 [PubMed] Maeno K et al: "Molecular basis for reduced estrone sulfate transport and altered modulator sensitivity of transmembrane helix (TM) 6 and TM17 mutants of multidrug resistance protein 1 (ABCC1)."
No. Sentence Comment
29 In contrast, substitution of TM17-Trp1246 with Phe, Tyr, Ala, or Cys selectively eliminates E217betaG and NNAL-O-glucuronide transport and drug resistance but has little or no effect on LTC4 and GSH transport (Ito et al., 2001a; Leslie et al., 2001a).
X
ABCC1 p.Trp1246Phe 19398503:29:34
status: NEW
Login to comment

PMID: 19949927 [PubMed] Chang XB et al: "Molecular mechanism of ATP-dependent solute transport by multidrug resistance-associated protein 1."
No. Sentence Comment
104 Mutations of C43S in TM1 (112); P343A, K332L and K332D in TM6 (113, 114); W445A and P448A in TM8 (113, 115); T550A, T556A and P557A in TM10 (113, 116); N590A, F594A, P595A, N597A, S604A and S605A in TM11 (113, 117, 118); E1089Q, E1089A, E1089L, E1089N, K1092, S1097 and N1100 in TM14 (119, 120); R1197K in TM16 (121); Y1236F, T1241A, T1242A, T1242C, T1242S, T1242L, Y1243F, N1245A, W1246C, W1246A, W1246F, W1246Y or R1249K in TM17 (121-124) significantly affect MRP1 function.
X
ABCC1 p.Trp1246Phe 19949927:104:398
status: NEW
Login to comment

PMID: 21143116 [PubMed] He SM et al: "Structural and functional properties of human multidrug resistance protein 1 (MRP1/ABCC1)."
No. Sentence Comment
763 In contrast, substitution of Trp1246 with Phe, Tyr, Ala, or Cys selectively eliminated E217 G and NNAL-O-glucuronide transport and drug resistance but showed little or no effect on LTC4 and GSH transport [166, 341, 371].
X
ABCC1 p.Trp1246Phe 21143116:763:29
status: NEW
Login to comment