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13.7: ATP Driven Pumps III: V-type Pumps

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ATP Driven Pumps III: V-type Pumps
 
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13.7: ATP Driven Pumps III: V-type Pumps

V-type pumps are ATP-driven pumps found in the vacuolar membranes of plants, yeast, endosomal and lysosomal membranes of animal cells, plasma membranes of a few specialized eukaryotic cells, and some prokaryotes. They are also known as the V1Vo-ATPase, that couple ATP hydrolysis to transport protons against a concentration gradient.

The peripheral or cytosolic V1 domain with eight subunits is involved in ATP hydrolysis. The integral or transmembrane V0 domain containing at least five subunits helps transport protons. This proton translocation activity is vital for cellular processes such as pH homeostasis, endocytosis, protein trafficking, urine acidification, and neurotransmitter release.

While complete loss of the pump function can be lethal, mutations in the subunits are associated with renal tubular acidosis, osteoporosis, neurodegenerative disease, and others, making this pump a potential drug target.

Regulation of the pumps’ activity by different mechanisms ensures that the cell and its organelles maintain the proton gradient. The reversible dissociation of the V0 and V1 domains is due to several factors like nutrients and growth factors that can silence the activity of both subunits. For instance, the reversible disulfide bond formation at the cysteine residues of the A-subunit does not allow ATP hydrolysis to occur.

Modulation of the pump density is another control mechanism seen in epithelial cells. In renal epithelial cells, proton transport in alpha intercalated and epididymal clear cells is controlled by reversible fusion of intracellular vesicles containing a high density of V-type pumps with the apical membrane. 


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ATP-driven Pumps V-type Pumps Vacuolar Membranes Plant Cells Yeast Cells Animal Cells Endosomal Membranes Lysosomal Membranes Plasma Membranes Eukaryotic Cells Prokaryotes V1Vo-ATPase ATP Hydrolysis Proton Transport Concentration Gradient PH Homeostasis Endocytosis Protein Trafficking Urine Acidification Neurotransmitter Release Renal Tubular Acidosis Osteoporosis Neurodegenerative Disease Drug Target Regulation Of Activity Reversible Dissociation Disulfide Bond Formation Cysteine Residues Control Mechanism

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