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PMID: 15835752
Takada T, Suzuki H, Sugiyama Y
Characterization of polarized expression of point- or deletion-mutated human BCRP/ABCG2 in LLC-PK1 cells.
Pharm Res. 2005 Mar;22(3):458-64.,
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
36
ABCG2 p.Asn596Ala
X
ABCG2 p.Asn596Ala 15835752:36:79
status:
VERIFIED
view ABCG2 p.Asn596Ala details
ABCG2 p.Asn418Ala
X
ABCG2 p.Asn418Ala 15835752:36:72
status:
VERIFIED
view ABCG2 p.Asn418Ala details
ABCG2 p.Cys592Ala
X
ABCG2 p.Cys592Ala 15835752:36:107
status:
VERIFIED
view ABCG2 p.Cys592Ala details
Using the site-directed mutagenesis technique, several mutants of BCRP (
N418A
,
N596A
, N418A&N596A BCRP and
C592A
, C603A&C608A, C592A&C603A&C608A BCRP) were constructed on pcDNA3.1(+) vector.
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57
ABCG2 p.Asn596Ala
X
ABCG2 p.Asn596Ala 15835752:57:142
status:
VERIFIED
view ABCG2 p.Asn596Ala details
ABCG2 p.Asn418Ala
X
ABCG2 p.Asn418Ala 15835752:57:97
status:
VERIFIED
view ABCG2 p.Asn418Ala details
Western blot analysis revealed that the modification was on the latter asparagine (Fig. 3B); the
N418A
mutant was N-glycosylated, whereas the
N596A
and N418A&N596A mutants did not exhibit any alteration in molecular weight following PNGase F treatment.
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61
ABCG2 p.Cys592Ala
X
ABCG2 p.Cys592Ala 15835752:61:118
status:
VERIFIED
view ABCG2 p.Cys592Ala details
Results of immunohistochemical staining suggested the importance of disulfide bonds on apical localization; a part of
C592A
mutant product seemed to be located on apical membrane, whereas other mutants appeared intracellularly (Fig. 4C).
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