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1.
Braz. j. med. biol. res ; 36(12): 1621-1627, Dec. 2003. ilus
Article in English | LILACS | ID: lil-350452

ABSTRACT

Trypsin is a serino-protease with a polypeptide chain of 223 amino acid residues and contains six disulfide bridges. It is a globular protein with a predominance of antiparallel á-sheet and helix in its secondary structure and has two domains with similar structures. We assessed the stability of á-trypsin in the acid pH range using microcalorimetric (differential scanning calorimetry) techniques. Protein concentrations varied in the range of 0.05 to 2.30 mg/ml. Buffer solutions of 50.0 mM á-alanine and 20.0 mM CaCl2 at different pH values (from 2.0 to 4.2) and concentrations of sorbitol (1.0 and 2.0 M), urea (0.5 M) or guanidinium hydrochloride (0.5 and 1.0 M) were used. The data suggest that we are studying the same conformational transition of the protein in all experimental situations using pH, sorbitol, urea and guanidinium hydrochloride as perturbing agents. The observed van't Hoff ratios (deltaHcal/deltaHvH) of 1.0 to 0.5 in the pH range of 3.2 to 4.2 suggest protein aggregation. In contrast, deltaHcal/deltaHvH ratios equal to one in the pH range of 2.0 to 3.2 suggest that the protein unfolds as a monomer. At pH 3.00, á-trypsin unfolded with Tm = 54ºC and deltaH = 101.8 kcal/mol, and the change in heat capacity between the native and unfolded forms of the protein (deltaCp) was estimated to be 2.50 ± 0.07 kcal mol-1 K-1. The stability of á-trypsin calculated at 298 K was deltaG D = 5.7 kcal/mol at pH 3.00 and deltaG D = 15.2 kcal/mol at pH 7.00, values in the range expected for a small globular protein.


Subject(s)
Animals , Cattle , Trypsin , Calorimetry, Differential Scanning , Hot Temperature , Hydrogen-Ion Concentration , Protein Denaturation , Thermodynamics , Trypsin
2.
Braz. j. med. biol. res ; 34(1): 35-44, Jan. 2001. tab, graf
Article in English | LILACS | ID: lil-277054

ABSTRACT

Hydrolysis of D-valyl-L-leucyl-L-arginine p-nitroanilide (7.5-90.0 `M) by human tissue kallikrein (hK1) (4.58-5.27 nM) at pH 9.0 and 37ºC was studied in the absence and in the presence of increasing concentrations of 4-aminobenzamidine (96-576 `M), benzamidine (1.27-7.62 mM), 4-nitroaniline (16.5-66 `M) and aniline (20-50 mM). The kinetic parameters determined in the absence of inhibitors were: Km = 12.0 + or - 0.8 `M and k cat = 48.4 + or - 1.0 min-1. The data indicate that the inhibition of hK1 by 4-aminobenzamidine and benzamidine is linear competitive, while the inhibition by 4-nitroaniline and aniline is linear mixed, with the inhibitor being able to bind both to the free enzyme with a dissociation constant Ki yielding an EI complex, and to the ES complex with a dissociation constant Ki', yielding an ESI complex. The calculated Ki values for 4-aminobenzamidine, benzamidine, 4-nitroaniline and aniline were 146 + or - 10, 1,098 + or - 91, 38.6 + or - 5.2 and 37,340 + or - 5,400 `M, respectively. The calculated Ki' values for 4-nitroaniline and aniline were 289.3 + or - 92.8 and 310,500 + or - 38,600 `M, respectively. The fact that Ki'>Ki indicates that 4-nitroaniline and aniline bind to a second binding site in the enzyme with lower affinity than they bind to the active site. The data about the inhibition of hK1 by 4-aminobenzamidine and benzamidine help to explain previous observations that esters, anilides or chloromethyl ketone derivatives of Nalpha-substituted arginine are more sensitive substrates or inhibitors of hK1 than the corresponding lysine compounds


Subject(s)
Humans , Aniline Compounds/pharmacology , Benzamidines/pharmacology , Chromogenic Compounds/metabolism , Oligopeptides/metabolism , Tissue Kallikreins/antagonists & inhibitors , Amidohydrolases/metabolism , Binding Sites , Hydrolysis , Linear Models , Tissue Kallikreins/metabolism , Trypsin Inhibitors/pharmacology
3.
Rev. argent. dermatol ; 80(2): 74-80, abr.-jun. 1999. ilus, tab
Article in Spanish | LILACS | ID: lil-248531

ABSTRACT

Se presentan dos casos de melanoma acral de localización imterdigital en una mujer de 67 años y en un hombre de 65. Se realiza una reseña bibliográfica de 28 trabajos de la literatura médica, con 843 casos de esta enfermedad. Se aprecia de este modo que la mayor frecuencia es la plantar seguida por la ungueal, siendo la ubicada en los espacios de los dedos, la de menor cuantía


Subject(s)
Humans , Male , Female , Aged , Foot Diseases/diagnosis , Foot Diseases/surgery , Melanoma/classification
5.
An. paul. med. cir ; 110(3): 5-10, 1983.
Article in Portuguese | LILACS | ID: lil-18495

ABSTRACT

Os autores historiam sucintamente as tecnicas de tratamento cirurgico da luxacao escapulo-umeral. Descrevem a tecnica de Bittar e comentam os resultados de 20 casos operados no Hospital da Beneficiencia Portuguesa de Sao Paulo,que aumentam a casuistica do metodo usado ha 25 anos


Subject(s)
Adolescent , Adult , Humans , Male , Female , Osteotomy , Shoulder Dislocation
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