Characterization of HeLa 5′-Nucleotidase: A Stable Plasma Membrane Marker

Abstract

5′-Nucleotidase, assayed as 5′-AMPase, has been extensively characterized and established as a stable, quantitative plasma membrane marker in HeLa S3 cells. The membrane 5′-AMPase has a K_m of 7.0 μM. Relative affinities of the other 5′-mononucleotides for the enzyme are 5′-GMP > 5′-TMP > 5′-UMP > 5′-CMP. There are activity optima at pH7 and 10; the latter is Mg²⁺-dependent. The membrane preparations have a small amount of acid phosphatase activity that is distinct from 5′-AMPase activity but no alkaline phosphatase. AOPCP, ADP, and ATP are strongly inhibitory. Mg²⁺, Ca²⁺, or Co²⁺ additions do not affect the pH 7.0 activity; Mn²⁺ activates slightly, whereas Zn²⁺, Cu²⁺, and Ni²⁺ are inhibitory. EDTA slowly inactivates, but removal of the EDTA without the addition of divalent cations restores activity. The inactivation is also substantially reversed by Co²⁺ or Mn²⁺, but reactivability by divalent cations decreases with time in EDTA. ConA strongly inhibits, and α-methyl-D-mannoside or glucose (the latter much less efficiently) relieves the inhibition, indicating that the 5′-AMPase is a glycoprotein. Histidine is also inhibitory. Ouabain, phloretin, cytochalasin B, cysteine, phenyl-alanine, MalNEt, and IAA are without effect.

5′-AMPase activity codistributes with pulse-bound [³H]ouabain when either of two cell fractionation procedures are used. The 5′-AMPase activity per cell is constant at different cell densities in exponentially growing cells, and activity per unit cell volume remains constant throughout the cell cycle. These properties, together with its absence in other organelles, its stability to storage, its insensitivity to certain experimental manipulations, and its general insensitivity to inhibitors of specific transport systems, make 5′-AMPase a useful quantitative marker in studies on the regulation of HeLa membrane transport systems.

Key Words:

• HeLa
• 5′-nucleotidase
• plasma membrane marker
• non-specific phosphatases
• divalent ions
• ConA
• AOPCP
• cell cycle
• mitochondria
• transport inhibitors