A Model for the Proteolipid Ring and Bafilomycin/Concanamycin-binding Site in the Vacuolar ATPase ofNeurospora crassa

Abstract

The vacuolar ATPase has been implicated in a variety of physiological processes in eukaryotic cells. Bafilomycin and concanamycin, highly potent and specific inhibitors of the vacuolar ATPase, have been widely used to investigate the enzyme. Derivatives have been developed as possible therapeutic drugs. We have used random mutagenesis and site-directed mutagenesis to identify 23 residues in the c subunit involved in binding these drugs. We generated a model for the structure of the ring of c subunits in Neurospora crassa by using data from the crystal structure of the homologous subunits of the bacterium Enterococcus hirae (Murata, T., Yamato, I., Kakinuma, Y., Leslie, A. G., and Walker, J. E. (2005) Science 308, 654 -659). In the model 10 of the 11 mutation sites that confer the highest degree of resistance are closely clustered. They form a putative drug-binding pocket at the interface between helices 1 and 2 on one c subunit and helix 4 of the adjacent c subunit. The excellent fit of the N. crassa sequence to the E. hirae structure and the degree to which the structural model predicts the clustering of these residues suggest that the folding of the bacterial and eukaryotic polypeptides is very similar. The vacuolar ATPase (V-ATPase)2 is a component of almost all the eukaryotic cell membranes derived from the endoplasmic reticulum, e.g. Golgi, vacuoles, and coated vesicles (1-4). It generates an electrochemical gradient for protons, providing a driving force for metabolite transport. It also plays a major role in adjusting the pH within organelles.In animals many diverse physiological processes depend on the function of the V-ATPase. For example, a single mutation of the enzyme in humans was shown to cause both loss of kidney function and deafness (5). The V-ATPase is critical for the growth of bone (6), and overexpression of the enzyme has been correlated with the metastasis of breast cancer cells (7). The common thread linking these physiological events is secretion of protons by specialized cells that have high amounts of V-ATPase in the plasma membrane. A high rate of proton transport by the V-ATPase appears to be a key element in the development of diseases such as osteoporosis and in the growth of certain types of tumors. These findings have led to an investigation of the use of V-ATPase inhibitors as therapeutic drugs (8, 9).Several different classes of natural products, such as the benzolactone enamides and the chondropsins, have been shown to be potent and specific inhibitors of V-ATPases (10 -12). The most widely used inhibitors are two similar macrolide antibiotics, bafilomycin and concanamycin. These molecules inhibit the V-ATPase from all eukaryotic cells that have been tested, typically with half-maximal inhibition at 0.1-5 nM when assayed in vitro (13-15). At higher concentrations these antibiotics also inhibit in vivo, and derivatives of bafilomycin were effective in treating osteoporosis in a rat model system (16).We have been trying to identify the site on the V-ATPase at which bafilomycin an...

Models for the a subunits of the Thermus thermophilus V/A-ATPase and Saccharomyces cerevisiae V-ATPase enzymes by cryo-EM and evolutionary covariance

“…Other than these differences, comparison of the two states reveals only minor conformational changes in individual subunits, suggesting little flexibility in the enzyme as a whole (Movie S3). The T. thermophilus V/A-ATPase thus seems to be relatively rigid compared with the S. cerevisiae V-ATPase (8) Numerous studies, many by Forgac and coworkers, have investigated the topology, function, and subunit arrangement of the S. cerevisiae V-ATPase V O region (31,34,(38)(39)(40)(41)(42)(43)(44). The model of the a subunit presented here is in excellent agreement with these studies.…”

“…Finally, studies of the a and c subunits identified residues that, when mutated, can lead to partial resistance to bafilomycin, an inhibitor of V-ATPases. Single and double mutants were made in the c subunit of Neurospora crassa, a mold whose c subunit sequence is 79% identical to that of the S. cerevisiae c subunit (43). Ten residues were proposed to participate in bafilomycin binding, all of which are conserved in S. cerevisiae.…”

“…(D) Residues that, when mutated (blue spheres) in the c subunit (T32, T39, L50, I54, V57, G61, L131, F135, L139, and Y142) and a subunit (E721, L724, and N725), give partial resistance to bafilomycin (43,44). The positions of these residues suggest a binding site for bafilomycin between two adjacent c subunits (pink and magenta) that is accessed via the a subunit (green ribbon).…”

Vacuolar ATPase depletion affects mitochondrial ATPase function, kinetoplast dependency, and drug sensitivity in trypanosomes

“…We next used an orthogonal chemical approach to assess the role of V-ATPase function in sensitizing T. brucei to ISM. Bafilomycin is a specific inhibitor of the V-ATPase that binds to the c subunit of V o (22). As predicted, and as demonstrated using isobologram analysis, bafilomycin strongly antagonizes ISM action (Fig.…”

Estimating the rotation rate in the vacuolar proton-ATPase in native yeast vacuolar membranes

“…Our data is compatible only with a single binding site per monomeric enzyme. Since concanamycin A most likely binds to intramembranous subunits Whyteside et al 2005;Bowman et al 2006;Dixon et al 2008), the present result suggests that an interaction with a single subunit c is not sufficient for concanamycin A binding: it either binds to more than one subunits or it binds to either subunit a, c' or c" (Huss et al 2002), of which there are only one copies in the structure, although its interaction with the lobster c ring and other recent data Bowman et al 2006;Dixon et al 2008) argue against c' and c'' being the binding sites. The accuracy of our approach could be further improved by adding more points to the inhibitor titration curve.…”