Mutational analysis of conserved aromatic residues in the A-loop of the ABC transporter ABCB1A (mouse Mdr3)

被引:10
作者
Carrier, Isabelle
Urbatsch, Ina L.
Senior, Alan E.
Gros, Philippe
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, McGill Canc Ctr, Montreal, PQ H3G 1Y6, Canada
[3] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
基金
加拿大健康研究院;
关键词
ABC transporter; ATP hydrolysis; Abcb1a; nucleotide-binding domain; site-directed mutagenesis;
D O I
10.1016/j.febslet.2006.12.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The A-loop is a recently described conserved region in the NBDs of ABC transporters [Ambudkar, SN., Kim, I.-W., Xia, D. and Sauna, Z.E. (2006) The A-loop, a novel conserved aromatic acid subdomain upstream of the Walker A motif in ABC transporters, is critical for ATP binding. FEBS Lett. 580,1049-1055; Kim, I.W., Peng, X.H., Sauna, Z.E., FitzGerald, P.C., Xia, D., Muller, M., Nandigama, K. and Ambudkar, SN. (2006) The conserved tyrosine residues 401 and 1044 in ATP sites of human P-glycoprotein are critical for ATP binding and hydrolysis: evidence for a conserved subdomain, the A-loop in the ATP-binding cassette. Biochemistry 45, 7605-76161. In mouse P-glycoprotein (Abcb1a), the aromatic residue of the Aloop in both NBDs is a tyrosine: Y397 in NBDI and Y1040 in NBD2. Another tyrosine residue (618 in NBDI and 1263 in NBD2) also appears to lie in proximity to the ATP molecule. We have mutated residues Y397, Y618, Y1040, and Y1263 to tryptophan and analyzed the effect of these substitutions on transport properties, ATP binding, and ATP hydrolysis by Abcb1a (mouse Mdr3). Y618W and Y1263W enzymes had catalytic characteristics similar to WT Abcbla. On the other hand, Y397W and Y1040W showed impaired transport and greatly reduced ATPase activity, including a similar to 10-fold increase in K-m for MgATP. Thus, Y397 and Y1040 play an important role in Abcb1a catalysis. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:301 / 308
页数:8
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