In vitro assembly of homopolymer and copolymer filaments from intermediate filament subunits of muscle and fibroblastic cells.
Open Access
- 1 June 1981
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 78 (6) , 3692-3696
- https://doi.org/10.1073/pnas.78.6.3692
Abstract
Evidence is presented that the intermediate filament (IF) subunits of [hamster stomach] muscle cells (skeleton or desmin) and fibroblastic cells (decamin or vimentin) separately form homopolymer IF in vitro and, when mixed, prefer to form copolymer IF in vitro. Because they coexist in cells, they may also form copolymers in vivo. The IF of baby hamster kidney fibroblasts (BHK-21) consist of a major subunit, decamin and 2 minor subunits which, on the basis of 2-dimensional gel and peptide mapping criteria, are identical to the .alpha.- and .beta.-subunits of smooth muscle desmin. The subunits differ only in their degrees of phosphorylation: .alpha.-desmin contained 2 mol/mol of O-phosphoserine whereas .beta.-desmin contained none. The decamin and desmin subunits assembled into homopolymer IF in vitro in high yield from purified denatured subunits under identical conditions of pH and ionic strength. Homopolymer decamin IF disassembled into soluble protofilaments in solutions of ionic strength < 0.05 mol/l whereas homopolymer desmin IF disassembled at ionic strength < 0.02 mol/l. When decamin and desmin were mixed together as denatured subunits or as soluble protofilaments, the IF assembled in vitro had solubility properties intermediate between those of the homopolymer IF, indicating that the 2 subunits had formed copolymer IF. The stoichiometry of copolymerization as determined in mixtures in which 1 subunit was present in excess was suggestive of the formation of 3 chain units. The possibility of nonspecific aggregation was eliminated by isolation of stable 3-chain .alpha.-helix-enriched particles from such IF. When tracer amounts of [35S]methionine-labeled decamin were mixed with desmin, labeled IF were obtained under conditions in which homopolymer decamin IF were soluble. These in vitro findings may be of physiological significance because native BHK-21 IF also had solubility properties similar to those of the copolymer IF.This publication has 39 references indexed in Scilit:
- Ultrastructural localization to 10 nm filaments of an insoluble 58K protein in cultured fibroblasts.Journal of Histochemistry & Cytochemistry, 1980
- In Vitro Reassembly of Squid Brain Intermediate Filaments (Neurofilaments): Purification by Assembly-DisassemblyScience, 1980
- Formation of 100 Å filaments from purified glial fibrillary acidic protein in VitroJournal of Molecular Biology, 1979
- Cytoplasmic Fibers in Mammalian Cells: Cytoskeletal and Contractile ElementsAnnual Review of Physiology, 1979
- HeLa cells contain intermediate-sized filaments of the prekeratin typeExperimental Cell Research, 1978
- The expression of keratin genes in epidermis and cultured epidermal cellsCell, 1978
- Structure of the three-chain unit of the bovine epidermal keratin filamentJournal of Molecular Biology, 1978
- Self-assembly of bovine epidermal keratin filaments in vitroJournal of Molecular Biology, 1976
- Neurofilament disguise, destruction and disciplineNature, 1975
- A Suggested Nomenclature for Fine-Structural Components of Keratin and Keratin-Like Products of CellsNature, 1964