Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C1275122 (TEM)
 21,810 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

beta-Lactamase activity was detected in cell-free preparations obtained from ultrasonic treatment of Neisseria gonorrhoeae after growth in liquid medium. Crude preparations of beta-lactamase were subjected to affinity chromatography, using several beta-lactam antibiotics as ligands bound to agarose supports. Affinity gels produced by coupling 7-aminocephalosporanic acid or 6-aminopenicillanic acid by their amino groups to carboxyl-terminal agarose via a five- to eight-carbon spacer arm proved to be effective chromatography media. beta-Lactamase preparations subjected to chromatography using these gels were purified 200-fold, with approximately 80% recovery of active material. Purified preparations were judged homogeneous by their behavior during electrophoresis on polyacrylamide in both the presence and absence of sodium dodecyl sulfate. Characterization of the purified enzyme established a molecular weight of approximately 25,000 and an isoelectric point of 5.4. Analyses of substrate specificity, effect of inhibitors, pH, and kinetic parameters were performed. The evidence suggests that the beta-lactamase produced in N. gonorrhoeae closely resembles the character of class IIIa (TEM-type) beta-lactamases.
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PMID:Purification by affinity chromatography and properties of a beta-lactamase isolated from Neisseria gonorrhoeae. 10 75

The results of ultrastructural studies and transmission electron microscope microanalysis of two Scenedesmus strains experimentally exposed to copper sulfate are presented. A fine-structural examination of the cells revealed the presence of nuclear inclusions in the form of central dense-core complexes. Cytoplasmic structures resembling the intranuclear inclusions were occasionally found in the cells. TEM-X-ray microanalysis of these structures has provided evidence that the inclusions contain copper. It is concluded that their presence may be regarded as a detoxifying mechanism.
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PMID:Intranuclear complexes in a copper-tolerant green alga. 125 45

The factors influencing the interaction of herpes simplex virus (HSV) glycoprotein C (gC) with the third component of complement (C3) were investigated in this study. The ability of gC of HSV type 1 (gC-1) to bind to the C3b fragment of C3 was found to be influenced by cell specific processing of gC-1 in a different manner, binding being remarkably enhanced in some cell lines following removal of sialic acid residues. Testing several intertypic recombinants of HSV we found that only strains expressing gC-1 exhibited binding to C3b, even though their genome consisted mainly of HSV-2 sequences in some recombinants. Expression of type-2 glycoproteins gB, gD, gE, gG, gH, and gI did not alter the ability of gC-1 to bind to C3b. Rosetting of HSV-1 infected Vero cells with C3b-coated red blood cells (EAC) was found to be temperature dependent and could be inhibited with purified C3b and anti-C3 antibodies. Polyanions like heparin or dextran sulfate were also inhibitory in a dose dependent manner, whereas C3d, neomycin and other aminoglycoside antibiotics failed to block. As the tested polyanions are also known to inhibit the infectivity of HSV, it could be speculated, that the complement binding function and the heparin-binding/attachment function of gC might be related.
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PMID:Factors influencing the interaction of herpes simplex virus glycoprotein C with the third component of complement. 133 54

Patients with chorea-acanthocytosis exhibit symptoms of self-biting, choreic movement, and acanthocytosis, but not dementia. The mechanism of choreic movements is still unknown. In order to clarify the etiologic mechanism underlying these movements, we evaluated the erythrocyte membrane in one patient with chorea-acanthocytosis. A 35-year-old female was admitted to Saitama Medical School Hospital because of involuntary movements. She was alert, well-oriented, and had no gross memory defects. She had slurred speech, choreic movements and lip biting. Laboratory examination showed acanthocytes in her peripheral red blood cells, normal serum lipid values, and caudate atrophy on her brain CT scan. In analyzing the acanthocytes, we initially evaluated the size of the acanthocyte population by incubating her red blood cells with plasma. The cell population approximately doubled after 2 hours incubation. Next we examined the protein composition of erythrocyte ghost by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). There was no significant difference between the patient's erythrocyte ghosts and those of a control. Then we investigated morphological changes in the patient's erythrocyte by scanning and transmission electron microscopy (SEM and TEM). SEM showed the typical acanthocyte shape. The quick-freeze, freeze-substitution method confirmed that the routine TEM section was not artifactual, and was in fact in accurate reflection of the actual features of acanthocytes. TEM of the sections prepared from erythrocyte ghosts demonstrated that spectrin tended to be accumulated in the thorn region. Furthermore, TEM of quick-freeze, deep-etched replica of the ghost revealed more clearly a spectrin network densely packed on the inner hydrophilic surface.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[Studies on the erythrocyte membrane skeleton in a patient with chorea-acanthocytosis--theoretical speculation on the mechanism of neurological involvement]. 141 52

Two crystal forms of Gram- bacteria TEM beta-lactamase have been obtained. The tetragonal form has a very large unit cell and diffracts to 3.0 A resolution. Orthorhombic crystals, grown using ammonium sulfate and a small amount of acetone as precipitating agents, belong to space group P2(1)2(1)2(1) with cell parameters a = 43.1 A, b = 64.4 A, c = 91.2 A and diffract to 1.7 A resolution. A seeding procedure has been designed that ensures reproducibility of the crystal properties. Molecular replacement, using a model reconstructed from the C alpha co-ordinates from Staphylococcus aureus PC1 beta-lactamase, gives a solution that satisfies crystal packing constraints.
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PMID:Crystallization and preliminary crystallographic data on Escherichia coli TEM1 beta-lactamase. 173 Oct 83

Picric acid-paraformaldehyde-glutaraldehyde (PA-P-G) was used to stabilize chemically ocular surface-associated mucus in mice of various ages. Transmission electron microscopy was then used to examine those specimens stained with cationic ferritin (CF), dialysed iron and Alcian Blue. Collectively, all of these stains are markers for anionic sulfate or carboxyl groups. With each of them, positive labeling of the ocular surface was observed for all ages examined, even when mucus cannot be morphologically demonstrated. Except for dialysed iron, staining was weak in the youngest animals and heaviest in young adult and aged mice. The ocular surface was negative for high iron diamine (HID) in pups and older mice through 1 year of age. Scant positive staining for HID was seen at the ocular surface in 14-month-old mice indicating that mucus became slightly sulfated with aging. Treatment of eyes with neuraminidase prior to fixation reduced the number of CF binding sites in all ages of mice examined, confirming that many of the carboxyl groups at the ocular surface are associated with sialic acid residues. Comparison of percentage reduction in CF labeling following neuraminidase treatment of the eyes of 5- and 10-postnatal day mice with all other ages of mice suggested that fewer removable carboxyl groups at the ocular surface are associated with sialic acid residues in pups. The ocular surface of all eyes also stained positively at the TEM level when a periodic acid-thiocarbohydrazide-silver protein (PA-T-SP) staining sequence was used. Collectively, these data are of significance with respect to further characterization of the ocular surface, particularly with regard to development-associated changes and their possible role in defence of the eye surface.
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PMID:Ocular surface complex carbohydrates are modified with aging. 243 68

The rare tyrosine-rich crystalloids (TRC) of salivary gland pleomorphic adenoma (PA) give a positive Million reaction indicating the presence of tyrosine. Their varied histochemical reactions, however, suggest a more complex composition. Two cases of TRC were encountered in a series of 144 PA (1.4%). Both were studied with several histochemical stains, and one tumor particularly rich in TRC was further examined with transmission and scanning electron microscopy and subjected to biochemical analysis using fresh-frozen tissue. TEM showed amorphous, electron-dense masses with no discernable internal structure. SEM revealed a geodelike structure of radially arranged, interlocking plates. Amino acid analysis of normal parotid, tumor with TRC, and a similar tumor without TRC indicated a slightly elevated level of tyrosine and arginine in the tumor with TRC. Polyacrylamide gel electrophoresis of tissue dissolved in sodium dodecyl sulfate revealed dense banding corresponding to polypeptides of a relative molecular weight of approximately 17,000 only in the TRC-rich sample. These bands on further analysis contained relatively large amounts of arginine. Tyrosine was present in only small amounts. TRC appear to be small proteins containing some tyrosine but rich in arginine.
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PMID:Tyrosine-rich crystalloids in pleomorphic adenoma: SEM findings and partial biochemical characterization. 285 75

Mild trypsinization of human erythrocyte stroma solubilized CR1 (complement receptor type 1, C3b/C4b receptor) without significant loss of decay-accelerating activity to C5 convertases on hemolytic intermediate cells (EAC 1-3b, P). The solubilized CR1 was purified using DEAE-Sephacel, C3-Sepharose, and anti-CR1-Sepharose column chromatographies. The purified material showed a single band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis under non-reducing conditions, and its molecular weight was determined to be 175K, about 20K smaller than native CR1. Because the purified sample was separated into the several segments by sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions, the molecule is considered to be nicked and those segments are associated by disulfide bonds. These results mean that a large portion of the CR1 molecule is present outside of the plasma membrane of erythrocytes, and the intramembranous and cytoplasmic domains are not necessary for decay-accelerating activity.
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PMID:Solubilization of active complement receptor type 1 (CR1) from human erythrocyte stroma with trypsin and its purification. 295 80

A fraction (60F) which had cytotoxic and antitumor activity could be obtained by precipitating cell-free extract (CFE) of group A streptococcus (Su strain) with a 50% to 60% saturation of ammonium sulfate. 60F exhibited a potent inhibitory effect on the incorporation of 3H-thymidine into various types of transplantable tumor cells. The activity of 60F was reduced by proteases and heating at 45 degrees C, but not by glycosidases and nucleases. Furthermore, 60F showed antitumor activity, such as cure and prolongation of life, in animals bearing EAC, MM-2, and S-180 tumors. These results show that 60F is probably protein and essentially exerts cytotoxic action against every cell line of tumor tested in vitro, and that the antitumor activity of 60F in vivo depends on the transplantability of tumor cells.
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PMID:Cytotoxic and antitumor effect of a fraction from cell-free extract of group A Streptococcus on transplantable tumor cells. 332 52

The effect of temperature and chemical modification on the interaction of the human erythrocyte Band 3 protein (the anion transport protein) with 4-acetamido-4'-isothiocyanostilbene 2,2'-disulfonate (SITS; Ki = 10 microM)-Affi-Gel 102 resin was studied. Band 3 binds to the affinity resin in two states; weakly bound, which is eluted by 1 mM 4-benzamido-4'-aminostilbene 2,2'-disulfonate (BADS; Ki = 2 microM), and strongly bound, which is eluted only under denaturing conditions by 1% lithium dodecyl sulfate (LDS). At 4 degrees C, most of band 3 was present initially in the weakly bound form and very little in the strongly bound form. With longer incubations at 4 degrees C, the weakly bound form was slowly converted to the strongly bound form. At 37 degrees C, most of Band 3 was rapidly converted to the strongly bound form, with some Band 3 still remaining in the weakly bound form. Band 3 dimers, labelled with 4,4'-diisothiocyanostilbene 2,2'-disulfonate (DIDS) in one monomer, did bind to immobilized SITS but did not become tightly bound upon incubation at 37 degrees C. Since the covalent attachment of DIDS to one monomer prevented the adjacent monomer from becoming tightly bound to immobilized SITS ligand, this observation suggests that the inhibitor-binding sites of the two adjacent monomers must be interacting with each other. When the inhibitor site of Band 3 was selectively modified by citrate in the presence of 1-ethyl-3-(3-azonia-4,4-dimethylpentyl)carbodiimide (EAC), Band 3 bound to the resin was more easily eluted by BADS, suggesting reduced affinity for immobilized SITS. However, citrate-modified Band 3 did become tightly bound upon incubation at 37 degrees C.
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PMID:Studies on the interaction of matrix-bound inhibitor with Band 3, the anion transport protein of human erythrocyte membranes. 339 12


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