Literature DB >> 2061408

Electron microscopic studies of chicken gizzard caldesmon and its complex with calmodulin.

K Mabuchi1, C L Wang.   

Abstract

Caldesmon samples mounted on a stage rotating about a horizontal axis were shadowed keeping the shadow angle at about 3 degrees. This technique minimizes background metal deposits compared with the conventional method. The identity of caldesmon was confirmed by comparing the images of caldesmon alone with those of the caldesmon-calmodulin complex. In these samples the caldesmon molecules appeared to be elongated; most were between 30 and 80 nm in length. The maximum length was in good agreement with the earlier estimate of 74 nm based on hydrodynamic studies. Our observations also suggested the presence of a rather rigid 30-40 nm stretch in the middle of the caldesmon molecule, which was always visible under rotary shadowing, and a flexible structure of about 20 nm in length at each end of the molecule, which may or may not be visible depending on their orientation on the mica surface. In the samples of caldesmon crosslinked with calmodulin, we noticed the existence of complexes containing two calmodulin molecules per caldesmon molecule, separated by a distance of 60 nm, consistent with the suggestion that each end of caldesmon can interact with calmodulin.

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Year:  1991        PMID: 2061408     DOI: 10.1007/bf01774033

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  14 in total

1.  Melting of myosin and tropomyosin: electron microscopic observations.

Authors:  K Mabuchi
Journal:  J Struct Biol       Date:  1990-05       Impact factor: 2.867

2.  Calmodulin purification and fluorescent labeling.

Authors:  J R Dedman; M A Kaetzel
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

3.  Caldesmon. Molecular weight and subunit composition by analytical ultracentrifugation.

Authors:  P Graceffa; C L Wang; W F Stafford
Journal:  J Biol Chem       Date:  1988-10-05       Impact factor: 5.157

Review 4.  Caldesmon: a calmodulin-binding actin-regulatory protein.

Authors:  K Pritchard; C J Moody
Journal:  Cell Calcium       Date:  1986-12       Impact factor: 6.817

5.  Smooth muscle caldesmon. Rapid purification and F-actin cross-linking properties.

Authors:  A Bretscher
Journal:  J Biol Chem       Date:  1984-10-25       Impact factor: 5.157

6.  Smooth muscle caldesmon is an extended flexible monomeric protein in solution that can readily undergo reversible intra- and intermolecular sulfhydryl cross-linking. A mechanism for caldesmon's F-actin bundling activity.

Authors:  W P Lynch; V M Riseman; A Bretscher
Journal:  J Biol Chem       Date:  1987-05-25       Impact factor: 5.157

7.  Caldesmon has two calmodulin-binding domains.

Authors:  C L Wang; L W Wang; R C Lu
Journal:  Biochem Biophys Res Commun       Date:  1989-07-31       Impact factor: 3.575

8.  Cloning and expression of a smooth muscle caldesmon.

Authors:  J Bryan; M Imai; R Lee; P Moore; R G Cook; W G Lin
Journal:  J Biol Chem       Date:  1989-08-15       Impact factor: 5.157

9.  The mechanism of Ca2+ regulation of vascular smooth muscle thin filaments by caldesmon and calmodulin.

Authors:  C W Smith; K Pritchard; S B Marston
Journal:  J Biol Chem       Date:  1987-01-05       Impact factor: 5.157

10.  Caldesmon is an elongated, flexible molecule localized in the actomyosin domains of smooth muscle.

Authors:  D O Fürst; R A Cross; J De Mey; J V Small
Journal:  EMBO J       Date:  1986-02       Impact factor: 11.598

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  24 in total

1.  Sarcomeric binding pattern of exogenously added intact caldesmon and its C-terminal 20-kDa fragment in skinned fibers of skeletal muscle.

Authors:  S M Frisbie; M C Reedy; L C Yu; B Brenner; J M Chalovich; T Kraft
Journal:  J Muscle Res Cell Motil       Date:  1999-04       Impact factor: 2.698

Review 2.  Actin and the smooth muscle regulatory proteins: a structural perspective.

Authors:  J L Hodgkinson
Journal:  J Muscle Res Cell Motil       Date:  2000-02       Impact factor: 2.698

3.  Myosin VI must dimerize and deploy its unusual lever arm in order to perform its cellular roles.

Authors:  Monalisa Mukherjea; M Yusuf Ali; Carlos Kikuti; Daniel Safer; Zhaohui Yang; Helena Sirkia; Virginie Ropars; Anne Houdusse; David M Warshaw; H Lee Sweeney
Journal:  Cell Rep       Date:  2014-08-21       Impact factor: 9.423

4.  Smooth muscle caldesmon modulates peristalsis in the wild type and non-innervated zebrafish intestine.

Authors:  J Abrams; G Davuluri; C Seiler; M Pack
Journal:  Neurogastroenterol Motil       Date:  2012-03       Impact factor: 3.598

5.  A long helix from the central region of smooth muscle caldesmon.

Authors:  C L Wang; J M Chalovich; P Graceffa; R C Lu; K Mabuchi; W F Stafford
Journal:  J Biol Chem       Date:  1991-07-25       Impact factor: 5.157

6.  Sequence of an avian non-muscle caldesmon.

Authors:  J Bryan; R Lee
Journal:  J Muscle Res Cell Motil       Date:  1991-08       Impact factor: 2.698

Review 7.  The molecular anatomy of caldesmon.

Authors:  S B Marston; C S Redwood
Journal:  Biochem J       Date:  1991-10-01       Impact factor: 3.857

8.  Immunocytochemical localization of caldesmon and calponin in chicken gizzard smooth muscle.

Authors:  K Mabuchi; Y Li; T Tao; C L Wang
Journal:  J Muscle Res Cell Motil       Date:  1996-04       Impact factor: 2.698

9.  Affinity and structure of complexes of tropomyosin and caldesmon domains.

Authors:  E J Hnath; C L Wang; P A Huber; S B Marston; G N Phillips
Journal:  Biophys J       Date:  1996-10       Impact factor: 4.033

10.  Mode of caldesmon binding to smooth muscle thin filament: possible projection of the amino-terminal of caldesmon from native thin filament.

Authors:  E Katayama; M Ikebe
Journal:  Biophys J       Date:  1995-06       Impact factor: 4.033

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