mProX™ Human ABCB11 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Transporter Cell Lines
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Published Data
Fig.1 Human bile salts exporter ABCB11.
In the presence or absence of 40 μM taurocholic and two inhibitors (GC glycocholic, TC taurocholic, TUDC tauroursodesoxycholic, Rif rifampicin, and Glib glibenclamide), the relative ATPase activity of ABCB11 is examined.
Ref: Wang, Liang, et al. "Cryo-EM structure of human bile salts exporter ABCB11." Cell Research 30.7 (2020): 623-625.
Pubmed: 32203132
DOI: 10.1038/s41422-020-0302-0
Research Highlights
In biliary secretion, the bile salt export pump (BSEP) is crucial. The disease known as progressive familial intrahepatic cholestasis type 2 (PFIC2), which manifests as severe jaundice and liver failure, is caused by mutations in the ABCB11 gene, which codes for BSEP.
Imagawa, Kazuo, et al. "Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasis." Journal of Human Genetics 63.5 (2018): 569-577.
Pubmed:
29507376
DOI:
10.1038/s10038-018-0431-1
Bile acids are a class of physiological surfactants generated from cholesterol that are necessary for the digestion of fats and fat-soluble vitamins.
Wang, Liang, et al. "Structures of human bile acid exporter ABCB11 reveal a transport mechanism facilitated by two tandem substrate-binding pockets." Cell Research 32.5 (2022): 501-504.
Pubmed:
35043010
DOI:
10.1038/s41422-021-00611-9