An in vitro assay reveals essential protein components for the "catch" state of invertebrate smooth muscle.

"Catch," a state where some invertebrate muscles sustain high tension over long periods of time with little energy expenditure (low ATP hydrolysis rate) is similar to the "latch" state of vertebrate smooth muscles. Its induction and release involve Ca(2+)-dependent phosphatase and cAMP-dependent protein kinase, respectively. Molecular mechanisms for catch remain obscure. Here, we describe a quantitative microscopic in vitro assay reconstituting the catch state with proteins isolated from catch muscles. Thick filaments attached to glass coverslips and pretreated with approximately 10(-4) M free Ca(2+) and soluble muscle proteins bound fluorescently labeled native thin filaments tightly in catch at approximately 10(-8) M free Ca(2+) in the presence of MgATP. At approximately 10(-4) M free Ca(2+), the thin filaments moved at approximately 4 microm/s. Addition of cAMP and cAMP-dependent protein kinase at approximately 10(-8) M free Ca(2+) caused their release. Rabbit skeletal muscle F-actin filaments completely reproduced the results obtained with native thin filaments. Binding forces >500 pN/microm between thick and F-actin filaments were measured by glass microneedles, and were sufficient to explain catch tension in vivo. Synthetic filaments of purified myosin and twitchin bound F-actin in catch, showing that other components of native thick filaments such as paramyosin and catchin are not essential. The binding between synthetic thick filaments and F-actin filaments depended on phosphorylation of twitchin but not of myosin. Cosedimentation experiments showed that twitchin did not bind directly to F-actin in catch. These results show that catch is a direct actomyosin interaction regulated by twitchin phosphorylation.

Catchin, a novel protein in molluscan catch muscles, is produced by alternative splicing from the myosin heavy chain gene.

Molluscan catch muscles contain polypeptides of 110-120 kDa in size which have the same partial amino acid sequences as those of the myosin heavy chain (MHC). Here we provide evidence that these polypeptides are major components only of the catch-type muscles (their estimated molar ratio to MHC is approximately 1:1) and they are alternative products of the MHC gene. Northern blot analysis of total RNA from Mytilus galloprovincialis catch muscles was carried out with fragments from the 3'-end of the MHC cDNA as probes. We detected two bands of 6.5 kb and 3.5 kb. The former corresponds to the MHC mRNA, and the latter is an mRNA coding for catchin, a novel myosin rod-like protein. By using a 5'-rapid amplification of cDNA ends (RACE) PCR method, the full-length cDNA of Mytilus catchin was cloned. It codes for a protein with a unique N-terminal domain of 156 residues (rich in serine, threonine, and proline), which includes a phosphorylatable peptide sequence. The rest of the sequence is identical with the C-terminal 830 residues of the MHC. We also analyzed Mytilus and scallop (Argopecten irradians) genomic DNAs and found that the 5'-end of the cDNA sequence was located in a large intron of the MHC gene in both species. Since catchin is abundantly expressed only in catch muscles and it is phosphorylatable, we suggest that it may play an important role in the catch contraction of molluscan smooth muscles.

Polypeptide composition of envelopes of spinach chloroplasts: two major proteins occupy 90% of outer envelope membranes.

Outer and inner envelope membranes of spinach chloroplasts were isolated using floatation centrifugation followed by sedimentation sucrose density gradient centrifugation after disruption of intact chloroplasts by freezing and thawing. Two major fractions with buoyant densities of 1.11 and 1.08 g cm-3 and a minor fraction with a density of 1.15 g cm-3 were obtained. They were identified as inner and outer envelope and thylakoid fractions, respectively by analyzing their polypeptide composition by high-resolution SDS-PAGE and the N-terminal sequences of their protein components. Due to the refinement of the isolation procedure, most of the ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO), which had always been observed as a contaminant, was eliminated from the outer envelope fraction. Application of high-resolution SDS-PAGE revealed that this fraction was rich in the low-molecular-mass outer envelope protein, E6.7 [Salomon et al. (1990) Proc. Natl. Acad. Sci. USA 87: 5778] and a protein with a molecular mass of 15 kDa which is homologous to the 16 kDa outer envelope protein of pea [Pohlmeyer et al. (1997) Proc. Natl. Acad. Sci. USA 94: 9504]. The two proteins account for 90% of the total proteins present in outer envelope membranes. Proteins which are suggested to function in translocation of nuclear-encoded polypeptides were not identified in the envelopes from spinach in the present study. Differences in the protein composition of outer envelope membranes are discussed based on the developemental stages of chloroplasts.

A study of cell death in Werdnig Hoffmann disease brain.

We examined the occurrence of apoptotic cell death in the autopsied brains of four patients with Werdnig Hoffmann disease (WH), using TdT-mediated DIG-dUTP nick end labeling (TUNEL) and immunohistochemistry for apoptosis-related proteins. Three of the four patients, aged over 6 months, exhibited TUNEL-positive cells in the lateral nuclei of the thalamus, and one of the three patients also had TUNEL-positive cells in the cerebral cortex. The labeled nuclei did not show characteristic features such as nuclear fragmentation or apoptotic bodies, and synaptophysin-positive granules were observed around some of the TUNEL-positive cells, although none of the antibodies against glial markers could visualize TUNEL-positive cells. TUNEL-positive cells were not observed in other regions examined, including the spinal cord, medulla and cerebellum or in the brains of three age-matched controls. There were neither immunopositive structures for bcl-2 or p53 nor alteration of in situ expression of bcl-xs/l or bax in any subject, and the TUNEL-positive cells lacked immunopositivity against apoptosis-related proteins. The presence of these TUNEL-positive cells might suggest latent neurodegeneration in the thalamus before central chromatolysis of neurons or neuronal loss appears, although it is not clear whether apoptotic cell death is involved in this degenerative process.

Bi-directional movement of actin filaments along long bipolar tracks of oriented rabbit skeletal muscle myosin molecules.

In actomyosin in vitro motility assays, orientation of myosin molecules affects their interaction with actin. We obtained long tracks of myosin molecules with uniform orientation. Bipolar filaments about 50 microm long were made from myosin rod prepared from molluscan smooth muscles, to which rabbit skeletal-muscle myosin bound, creating long synthetic thick-filaments. Movement of F-actin toward their center was much faster (4.7 +/- 0.6 microm s(-1)) than in the opposite direction (1.9 +/- 0.2 microm s(-1)), indicating that myosin molecules were arranged in the same orientation along each half of the bipolar filament. These complex thick-filaments permit measurement of actin movement over 20 microm of oriented skeletal myosin tracks facilitating mechanistic studies of actomyosin motility.