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Position 834 in TM6 plays an important role in cholesterol and phosphatidylcholine transport by ABCA1
Author(s) -
Shimpei Itoh,
Kohjiro Nagao,
Yasuhisa Kimura,
Michinori Matsuo,
Noriyuki Kioka,
Kazumitsu Ueda
Publication year - 2015
Publication title -
bioscience biotechnology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.509
H-Index - 116
eISSN - 1347-6947
pISSN - 0916-8451
DOI - 10.1080/09168451.2014.993358
Subject(s) - abca1 , atp binding cassette transporter 1 , cholesterol , phosphatidylcholine , reverse cholesterol transport , biochemistry , chemistry , mutant , atp binding cassette transporter , residue (chemistry) , amino acid , lipoprotein , membrane , phospholipid , transporter , gene
ATP-binding cassette protein A1 (ABCA1) plays a key role in eliminating excess cholesterol from peripheral cells by generating nascent high-density lipoprotein (HDL). However, it remains unclear whether both phospholipids and cholesterol are directly loaded onto apolipoprotein A-I (apoA-I) by ABCA1. To identify the amino acid residues of ABCA1 involved in substrate recognition and transport, we applied arginine scan mutagenesis to residues L821–E843 of human ABCA1 and predicted the environment to which each residue is exposed. The relative surface expression of each mutant suggested that residues L821–E843 pass through the plasma membrane as TM6, and the four residues (S826, F830, L834, and V837) of TM6 are exposed to the hydrophilic internal cavity of ABCA1. Furthermore, we showed that L834 is critical for the function of ABCA1.

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