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Distance variations between active sites of H+-pyrophosphatase determined by fluorescence resonance energy transfer
Journal article   Open access   Peer reviewed

Distance variations between active sites of H+-pyrophosphatase determined by fluorescence resonance energy transfer

Yun-Tzu Huang, Tseng-Huang Liu, Yen-Wei Chen, Chien-Hsien Lee, Hsueh-Hua Chen, Tsu-Wei Huang, Shen-Hsing Hsu, Shih-Ming Lin, Yih-Jiuan Pan, Ching-Hung Lee, …
Journal of Biological Chemistry, Vol.285(31), pp.23655-23664
30/07/2010

Abstract

Homodimeric H + -pyrophosphatase (H + -PPase; EC 3.6.1.1) is a unique enzyme playing a pivotal physiological role in pH homeostasis of organisms. This novel H + -PPase supplies energy at the expense of hydrolyzing metabolic byproduct, pyrophosphate (PP i ), for H + translocation across membrane. The functional unit for the translocation is considered to be a homodimer. Its putative active site on each subunit consists of PPi binding motif, Acidic I and II motifs, and several essential residues. In this investigation structural mapping of these vital regions was primarily determined utilizing single molecule fluorescence resonance energy transfer. Distances between two C termini and also two N termini on homodimeric subunits of H + -PPase are 49.3 ± 4.0 and 67.2 ± 5.7 Å, respectively. Furthermore, putative PP i binding motifs on individual subunits are found to be relatively far away from each other (70.8 ± 4.8 Å), whereas binding of potassium and substrate analogue led them to closer proximity. Moreover, substrate analogue but not potassium elicits significant distance variations between two Acidic I motifs and two His-622 residues on homodimeric subunits. Taken together, this study provides the first quantitative measurements of distances between various essential motifs, residues, and putative active sites on homodimeric subunits of H + -PPase. A working model is accordingly proposed elucidating the distance variations of dimeric H + -PPase upon substrate binding. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
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https://doi.org/10.1074/jbc.M110.134916View
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