Reassociation of microvillar core proteins: making a microvillar core in vitro.
Open Access
- 1 February 1989
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 108 (2) , 495-502
- https://doi.org/10.1083/jcb.108.2.495
Abstract
Intestinal epithelia have a brush border membrane of numerous microvilli each comprised of a cross-linked core bundle of 15-20 actin filaments attached to the surrounding membrane by lateral crossbridges; the cross-bridges are tilted with respect to the core bundle. Isolated microvillar cores contain actin (42 kD) and three other major proteins: fimbrin (68 kD), villin (95 kD), and the 110K-calmodulin complex. The addition of ATP to detergent-treated isolated microvillar cores has previously been shown to result in loss of the lateral cross-bridges and a corresponding decrease in the amount of the 110-kD polypeptide and calmodulin associated with the core bundle. This provided the first evidence to suggest that these lateral cross-bridges to the membrane are comprised as least in part by a 110-kD polypeptide complexed with calmodulin. We now demonstrate that purified 110K-calmodulin complex can be readded to ATP-treated, stripped microvillar cores. The resulting bundles display the same helical and periodic arrangement of lateral bridges as is found in vivo. In reconstitution experiments, actin filaments incubated in EGTA with purified fimbrin and villin form smooth-sided bundles containing an apparently random number of filaments. Upon addition of 110K-calmodulin complex, the bundles, as viewed by electron microscopy of negatively stained images, display along their entire length helically arranged projections with the same 33-nm repeat of the lateral cross-bridges found on microvilli in vivo; these bridges likewise tilt relative to the bundle. Thus, reconstitution of actin filaments with fimbrin, villin, and the 110K-calmodulin complex results in structures remarkably similar to native microvillar cores. These data provide direct proof that the 110K-calmodulin is the cross-bridge protein and indicate that actin filaments bundled by fimbrin and villin are of uniform polarity and lie in register. The arrangement of the cross-bridge arms on the bundle is determined by the structure of the core filaments as fixed by fimbrin and villin; a contribution from the membrane is not required.This publication has 33 references indexed in Scilit:
- Mapping of the microvillar 110K-calmodulin complex: calmodulin-associated or -free fragments of the 110-kD polypeptide bind F-actin and retain ATPase activityThe Journal of cell biology, 1988
- ATPase activity of the microvillar 110 kDa polypeptide‐calmodulin complex is activated in Mg2+ and inhibited in K+‐EDTA by F‐actinFEBS Letters, 1987
- The 110-kD protein-calmodulin complex of the intestinal microvillus is an actin-activated MgATPase.The Journal of cell biology, 1987
- Calcium-regulated cooperative binding of the microvillar 110K-calmodulin complex to F-actin: formation of decorated filaments.The Journal of cell biology, 1987
- Microvillus 110K-calmodulin: effects of nucleotides on isolated cytoskeletons and the interaction of the purified complex with F-actin.The Journal of cell biology, 1985
- The 110,000-dalton actin- and calmodulin-binding protein from intestinal brush border is a myosin-like ATPase.Journal of Biological Chemistry, 1984
- Characterization of the 110-kdalton actin-calmodulin-, and membrane-binding protein from microvilli of intestinal epithelial cells.The Journal of cell biology, 1983
- Microfilament organization in the cytoskeleton of the intestinal brush border.1983
- INDUCED MORPHOLOGICAL-CHANGES IN ISOLATED MICROVILLI - REGULATION OF MEMBRANE TOPOLOGY INVITRO BY SUBMEMBRANOUS MICROFILAMENTS1983
- The digestive function of the epithelium of the small intestineBiochimica et Biophysica Acta, 1961