ABCMdb

ABCB1 p.Asn820Cys

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Publications

PMID: 21589945 [PubMed] Klepsch F et al: "Exhaustive sampling of docking poses reveals binding hypotheses for propafenone type inhibitors of P-glycoprotein."

No. Sentence Comment

138 In addition, a recent cross-linking study further strengthened this by showing that an M1M cross-link between L175C and N820C did not prevent verapamil and rhodamine B to be transported [46]. Login to comment

PMID: 22700974 [PubMed] Loo TW et al: "The ATPase activity of the P-glycoprotein drug pump is highly activated when the N-terminal and central regions of the nucleotide-binding domains are linked closely together."

No. Sentence Comment

10 It was found that cross-linking of cysteines that lie close to the LSGGQ (P517C) and Walker A (I1050C) sites of NBD1 and NBD2, respectively, as well as the cytoplasmic extensions of TM segments 3 (D177C or L175C) and 9 (N820C) with a short cross-linker activated ATPase activity over 10-fold. Login to comment
106 The location of residues that were mutated to cysteine to test for the effect of cross-linking between NBD1 and NBD2 (P517C/I1050C), NBD1 and TMD2 (L443C/S909C), ICL1 and ICL3 (D177C/N820C), TM segments 2 and 11 (C137/A935C) or 6 and 12 (T333C/L975C) are shown. Login to comment
115 Cross-linking of ICL1 (TMD1) and ICL3 (TMD2) in Close Proximity Also Activates P-gp ATPase Activity-To test if cross-linking of other segments predicted to undergo large conformational changes during the reaction cycle would also activate P-gp ATPase activity, we performed cross-linking studies on mutant D177C/N820C. Login to comment
120 Membranes prepared from cells expressing mutant D177C/ N820C were treated with M4M and M17M. Login to comment
129 A, model showing predicted orientations of Leu175 , Asp177 , andAsn820 intheclosedconformation.B,membranespreparedfromHEK293 cells expressing the ICL1/ICL3 mutants D177C/N820C or L175C/N820C were treated with cross-linkers M1M, M4M, or M17M or no cross-linker (Control). Login to comment
132 C, membranes expressing mutants D177C/N820C or L175C/N820C were treated with or without (None) cross-linker and histidine-tagged P-gp isolated by nickel-chelate chromatography. Login to comment
136 It was found that the effect of cross-linking on ATPase of mutant D177C/N820C (Fig. 3C) was very similar to those observed for mutant P517C/I1050C (Fig. 2B). Login to comment
137 Prior to cross-linking, mutant D177C/N820C showed verapamil-stimulated ATPase activity that was similar to the Cys-less parent. Login to comment
138 The basal ATPase activity of the M4M cross-linked D177C/N820C mutant was similar to that of uncross-linked mutant assayed in the presence of verapamil (Fig. 3B). Login to comment
139 No further stimulation of ATPase activity was observed when the M4M cross-linked D177C/N820C was assayed in the presence of verapamil. Login to comment
143 In this study, we also observed that the majority of mutant L175C/N820C was cross-linked when the mutant was treated with 0.02 mM M1M at 20 °C while only a low level of cross-linking (about 25%) was observed when D177C/N820C was treated under the same conditions. Login to comment
144 Since D177C is predicted to have a more favorable orientation toward N820C compared with L175C (Fig. 3A), it would be expected that cross-linking of D177C/N820C would be more efficient than L175C/N820C. Login to comment
145 One possibility is that a separate M1M molecule preferentially modifies each cysteine of mutant D177C/ N820C as it was found that cross-linking was reduced when the concentration of M1M was increased (data not shown). Login to comment
146 We previously observed that mutant L175C/N820 only showed efficient cross-linking with a narrow concentration range of M1M (about 10-20 ␮M). Login to comment
150 We tested the effects of M4M and M17M cross-linking on the ATPase activity of mutant L175C/N820C and found that the effects were similar to those observed with mutant D177C/ N820C (Fig. 3C). Login to comment
151 Cross-linking of L175C/N820C with M4M highly activated the basal ATPase activity of the mutant while cross-linking with M17M caused little activation. Login to comment
152 The ATPase activity of M17M cross-linked L175C/N820C could still be highly activated when assayed in the presence of verapamil. Login to comment
158 In previous studies we showed that mutants C137/A935C (39) and L443C/ S909C (27) had verapamil-stimulated ATPase activities similar to Cys-less P-gp. Login to comment
163 These results indicate that stimulation of ATPase activity observed in M4M cross-linked mutants P517C/I1050C (Fig. 2B), D177C/N820C, or L175C/N820C (Fig. 3C) was likely a specific effect of trapping the protein in the closed conformation. Login to comment
194 Mutants that showed activation of ATPase after cross-linking with M4M (P517C/I1050C and D177C/N820C) were tested for inhibition of cross-linking. Login to comment
226 D, membranes prepared from cells expressing mutant P517C/I1050C were pretreated without (None) or with 0.03 mM tariquidar (Tar) followed by incubation in the absence (-) or presence (ϩ) of 0.05 mM M4M cross-linker. Samples were then subjected to immunoblot analysis. Login to comment
233 Cross-linking P517C/I1050C (or D177C/ N820C) with M4M would hold the Walker A and LSGGQ sites in close proximity (Fig. 7A) to increase the probability of generating the ATP-bound sandwich conformation and therefore increase the basal ATPase activity. Login to comment
236 The observation that cross-linked mutants P517C/I1050C, D177C/N820C, and L175C/N820C showed high levels of ATPase activity indicates that the protein does not have to adopt an inward-facing conformation with separation of the NBDs for ATP hydrolysis to continue after the first two hydrolysis steps. Login to comment
264 We predict that covalent attachment of thiol-reactive drug substrates to cysteines in the TMDs (or M4M cross-linking of mutants P517C/I1050C, D177C/N820C, or L175C/N820C) traps P-gp in states IV-VI (Fig. 8) that show a high rate of ATP hydrolysis. Login to comment
104 The location of residues that were mutated to cysteine to test for the effect of cross-linking between NBD1 and NBD2 (P517C/I1050C), NBD1 and TMD2 (L443C/S909C), ICL1 and ICL3 (D177C/N820C), TM segments 2 and 11 (C137/A935C) or 6 and 12 (T333C/L975C) are shown. Login to comment
113 Cross-linking of ICL1 (TMD1) and ICL3 (TMD2) in Close Proximity Also Activates P-gp ATPase Activity-To test if cross-linking of other segments predicted to undergo large conformational changes during the reaction cycle would also activate P-gp ATPase activity, we performed cross-linking studies on mutant D177C/N820C. Login to comment
117 Membranes prepared from cells expressing mutant D177C/ N820C were treated with M4M and M17M. Login to comment
126 A, model showing predicted orientations of Leu175 , Asp177 , andAsn820 intheclosedconformation.B,membranespreparedfromHEK293 cells expressing the ICL1/ICL3 mutants D177C/N820C or L175C/N820C were treated with cross-linkers M1M, M4M, or M17M or no cross-linker (Control). Login to comment
133 It was found that the effect of cross-linking on ATPase of mutant D177C/N820C (Fig. 3C) was very similar to those observed for mutant P517C/I1050C (Fig. 2B). Login to comment
134 Prior to cross-linking, mutant D177C/N820C showed verapamil-stimulated ATPase activity that was similar to the Cys-less parent. Login to comment
135 The basal ATPase activity of the M4M cross-linked D177C/N820C mutant was similar to that of uncross-linked mutant assayed in the presence of verapamil (Fig. 3B). Login to comment
140 In this study, we also observed that the majority of mutant L175C/N820C was cross-linked when the mutant was treated with 0.02 mM M1M at 20 &#b0;C while only a low level of cross-linking (about 25%) was observed when D177C/N820C was treated under the same conditions. Login to comment
141 Since D177C is predicted to have a more favorable orientation toward N820C compared with L175C (Fig. 3A), it would be expected that cross-linking of D177C/N820C would be more efficient than L175C/N820C. Login to comment
142 One possibility is that a separate M1M molecule preferentially modifies each cysteine of mutant D177C/ N820C as it was found that cross-linking was reduced when the concentration of M1M was increased (data not shown). Login to comment
147 Cross-linking of L175C/N820C with M4M highly activated the basal ATPase activity of the mutant while cross-linking with M17M caused little activation. Login to comment
148 The ATPase activity of M17M cross-linked L175C/N820C could still be highly activated when assayed in the presence of verapamil. Login to comment
189 Mutants that showed activation of ATPase after cross-linking with M4M (P517C/I1050C and D177C/N820C) were tested for inhibition of cross-linking. Login to comment
229 The observation that cross-linked mutants P517C/I1050C, D177C/N820C, and L175C/N820C showed high levels of ATPase activity indicates that the protein does not have to adopt an inward-facing conformation with separation of the NBDs for ATP hydrolysis to continue after the first two hydrolysis steps. Login to comment
257 We predict that covalent attachment of thiol-reactive drug substrates to cysteines in the TMDs (or M4M cross-linking of mutants P517C/I1050C, D177C/N820C, or L175C/N820C) traps P-gp in states IV-VI (Fig. 8) that show a high rate of ATP hydrolysis. Login to comment

PMID: 20394729 [PubMed] Loo TW et al: "Human P-glycoprotein is active when the two halves are clamped together in the closed conformation."

No. Sentence Comment

7 Only mutant L175C/N820C was cross-linked. Login to comment
58 The majority of mutant L175C/N820C was cross-linked after treatment with M1M cross-linker (Fig. 2A). Login to comment
59 Cross-linked product was not observed in the other 11 mutants (Fig. 2A) or in the single cysteine mutants L175C and N820C (data not shown). Login to comment
60 When mutant L175C/N820C was treated with various concentrations of M1M, it was found that the highest amount of cross-linked product was obtained in the presence of about 0.01-0.02 mM cross-linker and decreased with higher concentrations of cross-linker (Fig. 2B). Login to comment
62 To test whether mutant L175C/N820C was still active, the histidine-tagged version of mutant L175C/N820C was isolated by nickel-chelate chromatography and assayed for drug-stimulated ATPase activity. Login to comment
64 It was found that activation and apparent affinity of mutant L175C/N820C for the drug substrates verapamil, vinblastine, rhodamine B, and colchicine were not significantly different from the Cys-less parent (data not shown). Login to comment
65 For example, mutant L175C/N820C showed 50% stimulation of ATPase activity (S50) in the presence of 12.6 ± 1.0 lM verapamil, 44 ± 7 lM rhodamine B, 450 ± 40 lM colchicine, and 2.2 ± 0.4 lM vinblastine. Login to comment
67 Therefore, the mutant was selected for further analysis. Cross-linking of mutant L175C/N820C with M1M (Fig. 2A) suggested that these residues were in close proximity. Login to comment
78 Mutant L175C/N820C was cross-linked with 0.02 mM M1M at 0 °C for various intervals in the presence of 0.3 mM verapamil or 5 mM Mg.ATP. Login to comment
83 Since mutant L175C/N820C was active, we tested the effect of cross-linking with M1M on drug-stimulated ATPase activity. Login to comment
84 Membranes prepared from cells expressing mutant L175C/N820C were first treated for 15 min at 0 °C in the presence or absence of M1M cross-linker. Login to comment
86 Fig. 4A shows that untreated mutant L175C/N820C exhibited about a 12-fold increase in verapamil-stimulated ATPase activity with basal and verapamil-stimulated ATPase activities of 0.14 and 1.75 lmol Pi/min/mg P-gp, respectively. Login to comment
92 We compared the effects of treating mutant L175C/N820C with low (0.02 mM; promotes cross-linking) or high (3 mM; inhibits cross-linking) concentrations of M1M on ATPase activity. Login to comment
93 Treatment of the mutant L175C/N820C with 0.02 mM M1M elevated the basal ATPase activity (Fig. 4A) while treatment with 3 mM cross-linker yielded ATPase activities that were similar to those of untreated control (data not shown). Login to comment
94 It was also found that the activity of mutants containing only L175C or N820C mutation was not affected by treatment with 0.02 mM M1M. Login to comment
97 Verapamil and rhodamine B were selected for study because thiol-reactive derivatives of these drug substrates have been used extensively in cysteine mutagenesis studies to characterize the X-link 170 kDa + + + _ + ++ + + + T176C D177C D178C L175C T176C D177C D178C L175C N820C + D821C + M1M A822C + ++ + T176C D177C D178C L175C B 0.0003 0.001 0.003 0.009 0.027 0.08 0.24 0.73 [M1M] (mM) X-link 170 kDa 0 2.2 C 0 20 40 60 80 100 PercentCross-linked 0.0003 0.001 0.003 0.009 0.027 0.08 0.24 0.73 [M1M] (mM) 0 2.2 A Fig. 2. Login to comment
100 (B) Mutant L175C/N820C was treated with various concentrations of M1M cross-linker for 15 min at 0 °C. Login to comment
104 Effect of ATP and verapamil on cross-linking of mutant L175C/N820C. Login to comment
105 (A) Membranes from cells expressing mutant L175C/N820C were incubated in the presence of no drug (None), 0.3 mM verapamil (+ verapamil) or 5 mM ATP plus 10 mM MgCl2 (+ Mg.ATP) for 15 min at 0 °C. Login to comment
111 Fig. 4B shows that untreated mutant L175C/N820C showed 50% stimulation (S50) of ATPase activity with 12.6 ± 1.0 lM verapamil and 44 ± 7 lM rhodamine B. Login to comment
113 Mutant L175C/N820C cross-linked with M1M showed an S50 of 4.3 ± 0.4 lM and 7.8 ± 0.8 lM for verapamil and rhodamine B, respectively. Login to comment
114 We also tested the activity of untreated and M1M-treated mutant L175C/N820C in the presence of various concentrations of ATP. Login to comment
121 The cross-linking results, however, suggest that L175C/N820C were already in close proximity in the absence of drug substrate or ATP (Figs. Login to comment
138 M1M-cross-linked mutant L175C/N820C still showed drug-stimulated ATPase activity with drug substrates verapamil and rhodamine B (Fig. 4B). Login to comment

PMID: 24275649 [PubMed] Loo TW et al: "Locking intracellular helices 2 and 3 together inactivates human P-glycoprotein."

No. Sentence Comment

114 Cross-linking of IH2 and IH3 Inhibits Activity-In a previous cysteine mutagenesis and cross-linking study, we showed that clamping ICL3 (N820C) in close proximity to ICL1 (D175C or D177C) by cross-linking cysteines with short cross-linkers activated P-gp ATPase activity (15, 33). Login to comment

PMID: 24523403 [PubMed] Loo TW et al: "Identification of the distance between the homologous halves of P-glycoprotein that triggers the high/low ATPase activity switch."

No. Sentence Comment

10 To determine the distance that show high or low ATPase activity, we cross-linked reporter cysteines L175C (N-half) and N820C (C-half) with cross-linkers of various lengths that separated the halves between 6 and 30 &#c5; (ॷ-carbons). Login to comment
48 The L175C and N820C reporter cysteines were selected because they are located at positions predicted to undergo large changes in distance between the closed (12 &#c5; between ॷ-carbons) and open (about 30 &#c5; between ॷ-carbons) conformations. Login to comment
49 In addition, modifications to L175C and N820C are not expected to have a major impact on activity because they reside outside the drug- and ATP-binding sites. Login to comment
50 We previously showed that L175C/N820C could be efficiently cross-linked with the short cross-linker 1,4-butanediyl bismethanethiosulfonate (M4M) that can span a distance of 7.5 &#c5; (about 13 &#c5; between ॷ-carbons) to activate ATPase activity (40). Login to comment
51 Here, we tested the effects of cross-linking mutant L175C/ N820C at 10 different distances between the halves. Login to comment
52 It was found that linkage of L175C to N820C with cross-linkers predicted to span a distance of less than 20 &#c5; highly activated P-gp ATPase activity (over 10-fold), but cross-linking with longer cross-linkers yielded P-gps with low ATPase activity. Login to comment
55 Mutations L175C and N820C were introduced into Cys-less P-gp as described previously (42). Login to comment
60 Disulfide Cross-linking Analysis-The double cysteine mutant L175C/N820C was transiently expressed in HEK 293 cells. Login to comment
66 Intramolecular disulfide cross-linking between L175C and N820C can be detected because the cross-linked product migrates with a slower mobility on SDS-polyacrylamide gels (47). Login to comment
68 Cross-linking of L175C/N820C with M1M or oxidant (copper phenanthroline) was performed using P-gp isolated by nickel-chelate chromatography. Login to comment
81 P-gp ATPase Activity Is Highly Activated When Residues L175C and N820C Are Cross-linked in Close Proximity-In a previous study, we found that cross-linking the two homologous halves through formation of a direct disulfide bond between A259C in intracellular helix 2 (IH2) and W803C in IH3 inhibited activity (49). Login to comment
83 Because cysteines at positions L175C and N820C are located away from the IH TMD/NBD contact points (Fig. 1), cross-linking L175C and N820C in close proximity might not disrupt TMD/NBD interactions. Login to comment
84 The L175C or N820C mutations did not appear to affect activity of P-gp because the drug-stimulated ATPase activity of the L175C/N820C mutant was very similar to the Cys-less parent (42). Login to comment
86 Cross-linking of mutant L175C/N820C was low (b0d;50% cross-linking) when membranes prepared from transfected cells were treated with oxidant (copper phenanthroline) even at 37 &#b0;C (data not shown). Login to comment
88 Accordingly, histidine-tagged mutant L175C/N820C was expressed in HEK 293 cells, isolated by nickel chelate chromatography and treated with oxidant. Login to comment
89 In the presence of dodecyl maltoside detergent, mutant L175C/ N820C could be efficiently cross-linked with copper phenanthroline (Fig. 2, A and B). Login to comment
101 Cross-linking of L175C and N820C in close proximity highly activates P-gp basal ATPase activity. Login to comment
102 A, purified histidine-tagged mutant L175C/N820C was treated with (af9;) or without (afa;) copper phenanthroline (CuP) or M1M cross-linker. Login to comment
105 B, amount of cross-linked protein relative to total P-gp was quantitated from three different transfections afe; S.D. C, ATPase activities of mutant L175C/N820C were determined in the absence (afa;) or presence (af9;) of verapamil (Ver) before (None) and after cross-linking with copper phenanthroline or M1M. Login to comment
107 To test for the effects of cross-linking on activity, isolated L175C/N820C was treated with or without 0.5 mM copper phenanthroline or 0.009 mM M1M. Login to comment
112 Activation of mutant L175C/N820C basal ATPase activity with M1M was higher than previously observed using membranes (42) suggesting that the efficiency of cross-linking was improved using purified P-gp. Login to comment
115 P-gp ATPase Activity Is Not Highly Activated When Residues L175C and N820C Are Cross-linked with Long Cross-linkers- The next step was to test the effects of cross-linking with MTS cross-linkers that could span longer distances such as M2M (5.2 &#c5;), M4M (7.8 &#c5;), M5M (8.8 &#c5;), M6M (10.4 &#c5;), M8M (13 &#c5;), M11M (16.9 &#c5;), M14M (19 &#c5;) and M17M (22 &#c5;) (45). Login to comment
117 For example, we used 0.009 mM M1M to treat L175C/N820C because we previously showed that cross-linking efficiency was sharply reduced at lower concentrations (0.003 mM) or higher concentrations (0.027 mM) (42). Login to comment
118 Accordingly, membranes prepared from cells expressing mutant L175C/N820C were treated with various concentrations of MTS cross-linkers with various lengths of spacer arms for 10 min at 20 &#b0;C, and samples were subjected to immunoblot analysis. Login to comment
127 Membranes prepared from cells expressing mutant L175C/ N820C were first treated for 10 min at 20 &#b0;C in the absence or presence of 0.027 mM MTS cross-linkers of different lengths. Login to comment
129 Because mutant L175C/N820C was efficiently cross-linked with the MTS cross-linkers, we tested whether cross-linking affected activity. Login to comment
131 Cross-linking of L175C/N820C P-gp with various concentrations of M2M and M17M cross-linker. Login to comment
132 Membranes prepared from HEK 293 cells expressing mutant L175C/N820C were treated with various concentrations (0-2.2 mM) of M2M (A and B) or M17M (C and D) cross-linker. Login to comment
136 Activation Switch for P-gp ATPase Activity MARCH 21, 2014ߦVOLUME 289ߦNUMBER 12 JOURNAL OF BIOLOGICAL CHEMISTRY 8487 membranes and assayed for ATPase activity in the presence or absence of saturating concentrations (0.4 mM) of verapamil. Fig. 5 shows that untreated mutant L175C/N820C isolated from membranes exhibited about a 12-fold increase in verapamil-stimulated ATPase activity. Login to comment
139 By contrast, treatment of mutant L175C/ N820C with the intermediate size MTS cross-linkers (M2M, M4M, M5M, M6M, and M8M) that span maximum distances of about 5.2-13 &#c5; (distance of about 10.6-18.6 &#c5; between the ॷ-carbons) highly activated ATPase activity in the absence of verapamil. Login to comment
142 It appeared that cross-linking of mutant L175C/N820C with the intermediate size cross-linkers locked P-gp in an activated state resulting in high levels of ATPase activity in the absence or presence of drug substrates. Login to comment
143 A quite different effect was observed when mutant L175C/ N820C was treated with the long cross-linkers M11M, M14M, and M17M that could span maximum distances of about 16.9, 19, and 22 &#c5; in length, respectively (span distances of about 22 to 28 &#c5; between the ॷ-carbons) (Fig. 5). Login to comment
145 Cross-linking of mutant L175C/N820C with the intermediate size MTS cross-linkers like M2M increased the basal ATPase activity of the mutant (Fig. 5). Login to comment
147 To test these possibilities, a series of control experiments were carried out with L175C/N820C using M2M. Login to comment
150 We compared the effects of treating mutant L175C/N820C with low (0.027 mM; promotes cross-linking) or high (3 mM; likely labels each cysteine with a separate M2M molecule) concentrations of M2M on ATPase activity. Login to comment
154 Next, mutant histidine-tagged P-gps were constructed that contained only the L175C or N820C mutation alone to test if modification of only one cysteine had an impact on ATPase activity. Login to comment
159 Cross-linking of mutant L175C/N820C with cross-linkers of various lengths. Login to comment
160 A, membranes prepared from HEK 293 cells expressing mutant L175C/N820C were treated without (None) or with MTS cross-linkers of various lengths (MXM). Login to comment
164 ATPase activity of mutant L175C/N820C cross-linked with various MXM cross-linkers. Login to comment
165 Membranes were prepared from HEK 293 cells expressing mutant histidine-tagged L175C/N820C and cross-linked with various MXM cross-linkers (X afd; 2-17). Login to comment
169 These results show that activation of mutant L175C/N820C basal ATPase activity by M2M was due to cross-linking between the two cysteines. Login to comment
173 In agreement with the EPR and simulation studies (55), we found that the presence of ATP did not promote the formation of a more closed structure as it did not promote L175C/N820C cross-linking (42). Login to comment
174 We also found that verapamil did not promote or inhibit cross-linking of L175C/N820C (42). Login to comment
179 The experiments presented here show that human L175C/ N820C P-gp remains active when it is trapped in conformations with a wide range of separations between the halves (about 6-30 &#c5;). Login to comment
192 Activity of L175C/N820C, Cys-less, L175C, and N820C P-gp treated with various concentrations of M2M. Login to comment
193 A, histidine-tagged mutant L175C/N820C was isolated from membranes treated was treated without (None), low (0.027 mM), or high (3 mM) concentrations of M2M and ATPase activity determined in the absence (afa;) or presence (af9;) of verapamil (Ver). Login to comment
194 B, membranes expressing histidine-tagged mutant L175C/N820C, Cys-less, L175C, or N820C P-gp were treated without (afa;) or with (af9;) 0.027 mM M2M. Login to comment
197 Correlation of ATPase activity of L175C/N820C treated with cross-linkers of various lengths and the distance between the ॷ-carbons of L175C and N820C. Login to comment
198 The activity of mutant L175C/N820C cross-linked with MXM cross-linker (M1M (2), M2M (3), M4M (4), M5M (5), M6M (6), M8M (7), M11M (8), M14M (9), or M17M (10)) was compared with that treated with copper phenanthroline (1). Login to comment
211 Could P-gp still transport drug substrates when L175C/ N820C is cross-linked with short (M2M to M8M) cross-linkers? Login to comment
212 Unfortunately, it was not possible to use whole cell transport or drug resistance assays because cross-linking could not be detected when cells expressing the L175C/N820C mutant were treated with the MTS cross-linkers.3 The lack of cross-linking in whole cells could be due to the presence of intracellular thiol reductants such as glutathione that would not only react with the MTS cross-linkers but also reduce any disulfide bond. Login to comment
214 We predict, however, that P-gp cross-linked at L175C/ N820C with short cross-linkers should be able to bind substrates with relatively high affinity because it was reported that P-gp trapped in the closed vanadate-trapped transition state had similar affinity for the drug substrates verapamil, Hoechst 33342, cyclosporin A, vinblastine, colchicine, rhodamine B, and doxorubicin as in the relaxed (open) state (66). Login to comment

PMID: 25053414 [PubMed] Loo TW et al: "Cysteines introduced into extracellular loops 1 and 4 of human P-glycoprotein that are close only in the open conformation spontaneously form a disulfide bond that inhibits drug efflux and ATPase activity."

No. Sentence Comment

257 Direct cross-linking of the cysteines L175C and N820C (23) or cross-linking of mutant P571C/I1050C with the short 1,4-butanediyl bismethanethiosulfonate cross-linker (7.8 &#c5;) (24) highly activated P-gp ATPase activity over 10-fold in the absence of drug substrates. Login to comment
258 Cysteines L175C/N820C are located in the intracellular loops (Fig. 1, C and D), whereas cysteines P517C/I1050C are located in the NBDs (Fig. 1, C and D). Login to comment
259 An explanation for the difference is that linkage of the homologous halves at the L175C/N820C or P517C/I1050C sites would tend to favor the closed conformation (Fig. 1C) to FIGURE 9. Login to comment

PMID: 25068895 [PubMed] Prajapati R et al: "Translocation mechanism of P-glycoprotein and conformational changes occurring at drug-binding site: Insights from multi-targeted molecular dynamics."

No. Sentence Comment

325 In another recent experiment [69], Loo and Clarke tested the effects of cross-linking mutant L175C (ICL1)/N820C (ICL3) to determine the distance between N-terminal and C-terminal half of P-gp that show high or low ATPase activity. Login to comment
326 They observed that there was over 10 fold increase in basal ATPase activity when L175C was linked to N820C with cross-linkers predicted to span a distance of less than 20 &#c5;, and predicted that the ATPase activation switch appears to be turned on or off when this distance is less than or greater than 20 &#c5;, respectively. Login to comment