The N-terminal end of nebulin interacts with tropomodulin at the pointed ends of the thin filaments

Abigail S. McElhinny, Bernhard Kolmerer, Velia M. Fowler, Siegfried Labeit, Carol Gregorio

Research output: Contribution to journalArticle

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Abstract

Strict regulation of actin thin filament length is critical for the proper functioning of sarcomeres, the basic contractile units of myofibrils. It has been hypothesized that a molecular template works with actin filament capping proteins to regulate thin filament lengths. Nebulin is a giant protein (∼800 kDa) in skeletal muscle that has been proposed to act as a molecular ruler to specify the thin filament lengths characteristic of different muscles. Tropomodulin (Tmod), a pointed end thin filament capping protein, has been shown to maintain the final length of the thin filaments. Immunofluorescence microscopy revealed that the N-terminal end of nebulin colocalizes with Tmod at the pointed ends of thin filaments. The three extreme N-terminal modules (M1-M2-M3) of nebulin bind specifically to Tmod as demonstrated by blot overlay, bead binding, and solid phase binding assays. These data demonstrate that the N terminus of the nebulin molecule extends to the extreme end of the thin filament and also establish a novel biochemical function for this end. Two Tmod isoforms, erythrocyte Tmod (E-Tmod), expressed in embryonic and slow skeletal muscle, and skeletal Tmod (Sk-Tmod), expressed late in fast skeletal muscle differentiation, bind on overlapping sites to recombinant N-terminal nebulin fragments. Sk-Tmod binds nebulin with higher affinity than E-Tmod does, suggesting that the Tmod/nebulin interaction exhibits isoform specificity. These data provide evidence that Tmod and nebulin may work together as a linked mechanism to control thin filament lengths in skeletal muscle.

Original languageEnglish (US)
Pages (from-to)583-592
Number of pages10
JournalJournal of Biological Chemistry
Volume276
Issue number1
DOIs
StatePublished - Jan 5 2001

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Tropomodulin
Muscle
Skeletal Muscle
Actin Capping Proteins
Protein Isoforms
Erythrocytes
Sarcomeres
nebulin
Myofibrils
Actin Cytoskeleton
Fluorescence Microscopy
Actins
Assays
Microscopic examination
Proteins

ASJC Scopus subject areas

  • Biochemistry

Cite this

The N-terminal end of nebulin interacts with tropomodulin at the pointed ends of the thin filaments. / McElhinny, Abigail S.; Kolmerer, Bernhard; Fowler, Velia M.; Labeit, Siegfried; Gregorio, Carol.

In: Journal of Biological Chemistry, Vol. 276, No. 1, 05.01.2001, p. 583-592.

Research output: Contribution to journalArticle

McElhinny, Abigail S. ; Kolmerer, Bernhard ; Fowler, Velia M. ; Labeit, Siegfried ; Gregorio, Carol. / The N-terminal end of nebulin interacts with tropomodulin at the pointed ends of the thin filaments. In: Journal of Biological Chemistry. 2001 ; Vol. 276, No. 1. pp. 583-592.
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