Abstract
Nebulin is a family of giant sarcomere matrix proteins of 6OO-900 kDa in most vertebrate skeletal muscles. Recent sequence analysis suggests that human nebulin is mainly composed of a large number (> 200) of conserved repeats of ∼ 35 residues. Two cloned nebulin fragments, consisting of 6 and 8 of the repeats, have been expressed in E. coli using the pET3d vector. Both F-actin cosedimentation and solid-phase binding assays demonstrated a specific binding of these nebulin fragments to actin. This finding suggests that nebulin is a giant protein which binds actin at multiple sites in a template-manner. The presence of an actin-binding template protein in the skeletal muscle sarcomere may have significant implications in the assembly and function of the contractile apparatus.
Original language | English |
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Pages (from-to) | 93-96 |
Number of pages | 4 |
Journal | FEBS Letters |
Volume | 281 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - Apr 9 1991 |
Externally published | Yes |
Keywords
- Actin-binding protein
- cDNA expression in E. Coli
- ELISA
- Muscle thin filament
- Nebulin
ASJC Scopus subject areas
- Biophysics
- Structural Biology
- Biochemistry
- Molecular Biology
- Genetics
- Cell Biology