Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: EC:3.4.21.1 (chymotrypsin)
10,938 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The distribution of myosin isozymes in embryonic and adult chicken gizzard muscle were examined by electrophoresis in a non-denaturing gel system (pyrophosphate acrylamide gel electrophoresis), and both light and heavy chains of embryonic and adult myosin isozymes were compared. In pyrophosphate acrylamide gel electrophoresis, there were three isozyme components in embryonic gizzard myosin, but only one isozyme in adult gizzard myosin. The mobility of the fastest migrating embryonic isozyme was similar to that of the adult isozyme. The three embryonic isozymes differ from each other in the light chain distribution. Two of them contain an embryo-specific myosin light chain, which is characterized by its molecular weight and isoelectric point, whereas the other embryonic myosin isozyme contained the same light chains as the adult myosin. The pattern of peptide fragments of embryonic heavy chain produced by digestion with alpha-chymotrypsin in the presence of SDS was not distinguishable from that of adult myosin heavy chain. Thus there are myosin isozymes specific to embryonic gizzard muscle which exhibit embryo-specific light chain compositions, but are similar to adult gizzard myosin in their heavy chain structure.
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PMID:Changes in myosin isozymes during development of chicken gizzard muscle. 687 71

Evidence is presented that the removal of the alkali light chain subunit from myosin subfragment 1 results in the exposure of a site (or sites) at the carboxyl-terminal region of the heavy chain that is rapidly digested by both trypsin and alpha-chymotrypsin. In the case of trypsin digestion, cleavage at this site proceeds at a much higher rate than cleavage at the two other sensitive regions located in the interior of the primary structure of this chain. This initial cleavage is responsible for the generation, on further digestion with trypsin, of a carboxyl-terminal fragment about 3000 daltons smaller than the corresponding fragment formed by digestion of subfragment 1. The ability of the heavy chain to reassociate with alkali light chain at 4 degrees C in the presence of MgATP is essentially abolished by cleavage at this exposed site by either trypsin or chymotrypsin. These observations indicate that the alkali light chain is binding to, or is capable of perturbing, a region of the heavy chain adjacent to the subfragment 1/subfragment 2 "hinge" region and support recent proposals that both the DTNB light chain and the alkali light chain may be interacting and may be modulating this flexible region of the cross bridge.
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PMID:On the mode of the alkali light chain association to the heavy chain of myosin subfragment 1. Evidence for the involvement of the carboxyl-terminal region of the heavy chain. 688 36

Limited alpha-chymotryptic digestion of Ca2+-, calmodulin-dependent myosin light chain kinase partially purified from smooth muscle (turkey gizzard) yielded a Ca2+-independent form of the enzyme. Digestion to yield the Ca2+-independent kinase required the enzyme complexed with Ca2+-calmodulin; when digestion was performed on the apoenzyme, i.e., in the absence of Ca2+, the dependence of kinase activity on Ca2+ was retained. The Ca2+-independent kinase was purified by ion-exchange chromatography and shown to have an apparent molecular weight of approximately 80000. The specific activity of the freshly prepared enzyme was 6.5 +/- 0.2 mumol of Pi incorporated min-1 mg-1 in the presence of Ca2+ and 8.3 +/- 0.3 mumol min-1 mg-1 in the absence of Ca2+, using the isolated light chains of gizzard myosin as the substrate. The Ca2+-independent enzyme also phosphorylated the 20000-dalton light chains of purified myosin and crude actomyosin from turkey gizzard. The Km of the Ca2+-independent kinase for Mg2+-ATP (54 muM) was not significantly different from that of the native, CA2+-dependent enzyme (68 muM). These observations indicate maintenance of the integrity of the active site after digestion with alpha-chymotrypsin. It is suggested that the loss of Ca2+ sensitivity of the kinase after limited proteolysis is due to loss of the calmodulin-binding site from the 80000-dalton fragment. The two sites of phosphorylation by the cyclic AMP dependent protein kinase were also removed by the chymotryptic hydrolysis.
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PMID:Calcium-independent myosin light chain kinase of smooth muscle. Preparation by limited chymotryptic digestion of the calcium ion dependent enzyme, purification, and characterization. 689 83

A number of enzymes are currently in use for obtaining proteolytic subfragments of rabbit skeletal muscle myosin. Subfragment-1 can be obtained by papain digestion of polymeric myosin in the presence (Mg-S1) or absence (EDTA-S1) of divalent cations [Margossian, S.S., Lowey, S., & Barshop, B. (1975) Nature (London) 258, 163-166]. Subfragment-1 prepared by chymotrypsin is readily fractionated according to its alkali light-chain content into S1(A1) and S1(A2) [Weeds, A.G., & Taylor, R.S. (1975) Nature (London) 257, 54-56]. Digestion of soluble myosin by trypsin or chymotrypsin leads to heavy meromyosin (HMM) and light meromyosin (LMM). Many of these subfragments show extensive cleavages in the heavy- and/or light-chain region by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. In view of the widespread use of proteolytic subfragments in kinetics and structural studies, it was of interest to establish the extent of heterogeneity of these preparations under nondenaturing conditions by equilibrium centrifugation. Analysis of the fringe displacements by the computer programs of Roark & Yphantis [Roark, D.E., & Yphantis, D.A. (1969) Ann. N.Y. Acad. Sci. 164, 245-278] showed that for three initial loading concentrations, the molecular weight averages Mn, Mw, M2, were superimposable across the entire solution column for all S1 and HMM species. The same applied for the initial molecular weight averages of LMM and rod, except that with these highly asymmetric molecules, a small drop in molecular weight was observed toward the cell bottom as would be expected from excluded volume effects. We conclude that the subfragments of myosin are remarkably homogeneous in benign solvents, despite the existence of some cleavages in their primary structure.
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PMID:Homogeneity of myosin subfragments by equilibrium centrifugation. 701 75

The effects of various proteolytic enzymes on the high molecular weight protein (connectin) present in a direct sodium dodecyl sulfate extract of myofibrils from chicken breast muscle were studied in detail. To keep the high molecular weight proteins intact, myofibrils had to be prepared in the presence of EGTA. Trypsin, chymotrypsin, papain, and nagarse readily hydrolyzed connectin (doublet band of titin) and the band 3 protein (N2-line protein). Pepsin did not attack connectin, but digested the band 3 protein and myosin. Calcium-activated neutral proteinase hydrolyzed the band 3 protein, leaving connectin intact. On the other hand, serine protease digested connectin but not the band 3 protein.
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PMID:Connectin, an elastic protein of muscle. Effects of proteolytic enzymes in situ. 702 43

The proteolytic susceptibility of the subfragment 2/light meromyosin junction [heavy meromyosin (HMM) junction] of myosin was employed as a probe of the cross-bridge conformation. The proteolysis was carried out in the myofibrils where myosin assembled in arrays typical of the in vivo organization. When subfragment I formation was inhibited by saturating the Nbs2 [5,5'-dithiobis(2-nitrobenzoic acid)] light chains with Mg2+ ions, chymotrypsin attacked exclusively the HMM junction. The rate of this attack was assessed by measuring the rate of HMM formation by quantitative polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate and by following absorbance changes associated with the solubilization of myofibrillar suspensions. Under rigor conditions, the myofibrils were relatively resistant to the chymotryptic attack. The presence of MgAMP-PNP or MgPPi did not affect the rate of proteolytic attack. On the other hand, binding of MgADP had a powerful stimulating influence on the HMM site digestibility. The dissociation constant for the effect of MgADP was 10 microM less than Kd less than 50 microM. MgADP did not exercise its unique effect through destabilization of myosin filaments or through dissociation of the actomyosin complex. These results are explained in terms of a change in the myosin cross-bridge conformation brought about by the binding of MgADP to the active site.
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PMID:Magnesium adenosine 5'-diphosphate influences proteolytic susceptibility of myosin in myofibrils. 704 59

It has previously been shown that the binding of calcium and magnesium ions to the isolated metal-binding light chains, i.e. those dissociable by 5,5'-dithiobis(2-nitrobenzoate), of rabbit skeletal muscle myosin is moderated by phosphorylation and is accompanied by a sizeable conformational change. As judged by circular dichroism in the region of the aromatic Cotton effects, this conformational change occurs when calcium ions bind to the light chain in situ on the myosin head. Moreover the affinity for calcium is again changed by phosphorylation. The change in chymotryptic digestion patterns, in particular the protection of the head-rod junction in insoluble myosin, by divalent cations, has been used to obtain binding profiles. The results are consistent with the presence of a single class of independent sites, showing no cooperativity. The affinity of the site for both calcium and magnesium ions is enhanced by 1-2 orders of magnitude when the light chain in incorporated in the myosin heads. The effect of phosphorylation on the affinity persists in these circumstances, being marked for calcium and small for magnesium. On phosphorylation the calcium binding constant falls from 8 x 10(6) M-1 to 4 x 10(6) M-1 at physiological ionic strength, compared with 2.5 x 10(5) M-1 and 5 x 10(4) M-1 for the isolated light chains. The sensitivity of the proteolytic cleavage sites is affected by phosphorylation. Thus in the absence of calcium ions the yield of subfragment 1 at a low chymotrypsin concentration is substantially greater in dephosphorylated than phosphorylated myosin, whereas at saturating concentrations of calcium ions attack at the light meromyosin/heavy meromyosin junction is favoured by phosphorylation. These observations may signify a structural effect of phosphorylation on the prevailing interactions within the myosin filament in physiological solvent conditions.
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PMID:Phosphorylation and the binding of calcium and magnesium to skeletal myosin. 743 56

The myosin head (S1) consists of a wide, globular region that contains the actin- and nucleotide-binding sites and an alpha-helical, extended region that is stabilized by the presence of two classes of light chains. The essential light chain abuts the globular domain, whereas the regulatory light chain lies near the head-rod junction of myosin. Removal of the essential light chain by a mild denaturant exposes the underlying heavy chain to proteolysis by chymotrypsin. The cleaved fragment, or "motor domain" (MD), migrates as a single band on SDS-polyacrylamide gel electrophoresis, with a slightly greater mobility than S1 prepared by papain or chymotrypsin. Three-dimensional image analysis of actin filaments decorated with MD reveals a structure similar to S1, but shorter by an amount consistent with the absence of a light chain-binding domain. The actin-activated MgATPase activity of MD is similar to that of S1 in Vmax and Km. But the ability of MD to move actin filaments in a motility assay is considerably reduced relative to S1. We conclude that the globular, active site region of the myosin head is a stable, independently folded domain with intrinsic motor activity, but the coupling efficiency between ATP hydrolysis and movement declines markedly as the light chain binding region is truncated.
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PMID:A minimal motor domain from chicken skeletal muscle myosin. 779 23

Exposure of 3T3 fibroblasts to the phosphatase inhibitor, calyculin-A, induces marked morphological changes and the formation of an aggregate of actin and myosin connected to the nucleus by intermediate filaments (Hirano, K., L. Chartier, R. G. Taylor, R. E. Allen, N. Fusetani, H. Karaki, D. J. Hartshorne: J. Muscle Res. Cell Motil. 13, 341-353 (1992)). Vimentin was isolated from this complex and shown to be phosphorylated. At least 4 phosphorylation sites were indicated. These sites were distinct from those phosphorylated by the cAMP-dependent protein kinase. Limited proteolysis was used to define the domains in which phosphorylation occurred. Vimentin was isolated from 32P-labeled calyculin-A-treated cells and digested with thrombin and alpha-chymotrypsin. Proteolysis with thrombin limited the phosphorylation to either the central core or C-terminal domain. Proteolysis with alpha-chymotrypsin indicated that the multiple phosphorylation sites were restricted to the C-terminal domain of vimentin.
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PMID:Phosphorylation of vimentin in the C-terminal domain after exposure to calyculin-A. 826 79

In smooth muscle tissue, two or three isoforms of myosin heavy chain (MHC) have been reported (SM1, SM2, and/or NM). In mouse uterus tissue, four bands in the region of the MHC's can be resolved on high resolution SDS polyacrylamide gels. Western blots using smooth muscle (SM) MHC-specific and nonmuscle (NM) MHC-specific polyclonal antibodies show the upper two bands in the MHC region are SM isoforms, whereas the lower two bands are NM isoforms. One-dimensional peptide maps of these four bands show each to have a unique pattern of polypeptide fragments following alpha-chymotrypsin digestion. Developmental expression of myosin heavy chains (MHC) in mouse uterus, aorta, bladder, and stomach (6 ages, 10-150 days) was determined using tissue homogenates. In the uterus, both SM MHC's show an increase in relative content with increasing age, whereas the NM MHC's show a decrease. The mouse aorta shows a significant increase in the SM MHC's and a significant decrease in the NM MHC from day 10 to day 30, which is similar to data reported for the rat aorta. Whereas both the bladder and stomach contain relatively small amounts of NM MHC's (approximately 10% or less), these quantities do show decreases with development. The SM1:SM2 ratio for the uterus remains high (3.4 at 150 days) through development; the aorta, bladder, and stomach also start out high, but tend toward 1.0 in the 150-day animals. The presence of four MHC isoforms in the uterus with unique developmental regulation of expression is consistent with hypotheses of unique functional roles for these isoforms.
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PMID:Expression of four myosin heavy chain isoforms with development in mouse uterus. 840 56


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