Mapping the microtubule binding regions of calponin

Biochemistry. 2003 Feb 11;42(5):1274-82. doi: 10.1021/bi020336g.

Abstract

The smooth muscle basic calponin interacts with F-actin and inhibits the actomyosin ATPase in a calmodulin or phosphorylation modulated manner. It also binds in vitro to microtubules and its acidic isoform, present in nonmuscle cells, and co-localizes with microfilaments and microtubules in cultured neurons. To assess the physiological significance and the molecular basis of the calponin-microtubule interaction, we have first studied the solution binding of recombinant acidic calponin to microtubules using quantitative cosedimentation analyses. We have also characterized, for the first time, the ability of both calponin isoforms to induce the inhibition of the microtubule-stimulated ATPase activity of the cytoskeletal, kinesin-related nonclaret dysjunctional motor protein (ncd) and the abolition of this effect by calcium calmodulin. This property makes calponin a potent inhibitor of all filament-activated motor ATPases and, therefore, a potential regulatory factor of many motor-based biological events. By combining the enzymatic measurements of the ncd-microtubules system with various in vitro binding assays employing proteolytic, recombinant and synthetic fragments of basic calponin, we further unambiguously identified the interaction of microtubules at two distinct calponin sites. One is inhibitory and resides in the segment 145-182, which also binds F-actin and calmodulin. The other one is noninhibitory, specific for microtubules, and is located on the COOH-terminal repeat-containing region 183-292. Finally, quantitative fluorescence studies of the binding of basic calponin to the skeletal pyrenyl F-actin in the presence of microtubules did not reveal a noticeable competition between the two sets of filaments for calponin. This result implies that calponin undergoes a concomitant binding to both F-actin and microtubules by interaction at the former site with actin and at the second site with microtubules. Thus, in the living cells, calponin could potentially behave as a cross-linking protein between the two major cytoskeletal filaments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / chemistry
  • Actins / metabolism
  • Adenosine Triphosphatases / antagonists & inhibitors
  • Adenosine Triphosphatases / metabolism
  • Animals
  • Brain / enzymology
  • Brain / metabolism
  • Calcium-Binding Proteins / chemistry*
  • Calcium-Binding Proteins / metabolism*
  • Calcium-Binding Proteins / physiology
  • Calponins
  • Cattle
  • Drosophila Proteins*
  • Enzyme Activation / physiology
  • Enzyme Inhibitors / chemistry
  • Kinesins / antagonists & inhibitors
  • Kinesins / metabolism
  • Microfilament Proteins
  • Microtubule-Associated Proteins / chemistry*
  • Microtubule-Associated Proteins / metabolism*
  • Microtubule-Associated Proteins / physiology
  • Microtubules / chemistry*
  • Microtubules / enzymology
  • Microtubules / metabolism*
  • Molecular Motor Proteins / antagonists & inhibitors
  • Molecular Motor Proteins / enzymology
  • Muscle, Smooth / chemistry
  • Muscle, Smooth / enzymology
  • Myosins / antagonists & inhibitors
  • Myosins / metabolism
  • Peptide Fragments / chemistry*
  • Peptide Fragments / metabolism*
  • Peptide Mapping
  • Protein Binding
  • Rabbits
  • Rats
  • Swine
  • Turkeys

Substances

  • Actins
  • Calcium-Binding Proteins
  • Drosophila Proteins
  • Enzyme Inhibitors
  • Microfilament Proteins
  • Microtubule-Associated Proteins
  • Molecular Motor Proteins
  • Peptide Fragments
  • ncd protein, Drosophila
  • Adenosine Triphosphatases
  • Myosins
  • Kinesins