International journal of peptide and protein research最新文献_第10页

Hydrolysis of beta-casein by gastric proteases. I. Comparison of proteolytic action of bovine chymosin and pepsin A. 胃蛋白酶对-酪蛋白的水解。牛凝乳酶与胃蛋白酶A蛋白水解作用的比较。

International journal of peptide and protein research Pub Date : 1991-06-01

H Guillou, G Miranda, J P Pelissier

引用次数: 0

Enhancement of solubility by temporary dimethoxybenzyl-substitution of peptide bonds. Towards the synthesis of defined oligomers of alanine and of lysyl-glutamyl-glycine. 暂时二甲氧基苄取代肽键提高溶解度。合成丙氨酸和赖氨酸-谷氨酰-甘氨酸的低聚物。

International journal of peptide and protein research Pub Date : 1991-06-01

J Blaakmeer, T Tijsse-Klasen, G I Tesser

引用次数: 0

Infrared spectroscopic discrimination between alpha- and 3(10)-helices in globular proteins. Reexamination of Amide I infrared bands of alpha-lactalbumin and their assignment to secondary structures. 球形蛋白中α -和3(10)-螺旋的红外光谱区分。α -乳清蛋白酰胺I红外波段及其二级结构的重新研究。

International journal of peptide and protein research Pub Date : 1991-06-01

S J Prestrelski, D M Byler, M P Thompson

{"title":"Infrared spectroscopic discrimination between alpha- and 3(10)-helices in globular proteins. Reexamination of Amide I infrared bands of alpha-lactalbumin and their assignment to secondary structures.","authors":"S J Prestrelski, D M Byler, M P Thompson","doi":"","DOIUrl":"","url":null,"abstract":"We have undertaken a new and more detailed Fourier-transform infrared (FTIR) spectroscopic study of alpha-lactalbumin (in D2O solution) aimed at correlating its secondary structures to observed Amide I' infrared bands. The spectra reported here were interpreted in light of the recently determined crystal structure of alpha-lactalbumin and by comparison with the spectra and structure of the homologous protein lysozyme. Of particular importance is the new evidence supporting the assignment of the band at 1639 cm-1 to 3(10)-helices. This assignment is in excellent agreement with one based on theoretical and experimental studies of 3(10)-helical polypeptides. The frequency observed for 3(10)-helices is distinctly different from that at which alpha-helices are typically found (viz., around 1655 cm-1). In the present study, two bands are clearly resolved in the latter region at 1651 and 1659 cm-1. Both are apparently associated with alpha-helices. These results suggest that for D2O solutions of globular proteins. FTIR spectroscopy can be a facile method for detecting the presence of these two different types of helical conformation and distinguishing between them. This provides a distinct advantage over ultraviolet circular dichroism spectroscopy (UV-CD). This work also provides a basis for future studies of alpha-lactalbumin which examine the effects of environment (e.g., pH, temperature) and ligands (e.g., Ca2+, Mn2+) on its conformation.","PeriodicalId":14204,"journal":{"name":"International journal of peptide and protein research","volume":"37 6","pages":"508-12"},"PeriodicalIF":0.0,"publicationDate":"1991-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13077169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

2-Chlorotrityl chloride resin. Studies on anchoring of Fmoc-amino acids and peptide cleavage. 2-氯三烷基氯树脂。fmoc氨基酸的锚定与肽切割的研究。

International journal of peptide and protein research Pub Date : 1991-06-01

K Barlos, O Chatzi, D Gatos, G Stavropoulos

引用次数: 0

Conformation of MeAla6-cyclosporin A by NMR. Relationship of sidechain orientation of the MeBmt-1, MeLeu-9, and MeLeu-10 residues to immunosuppressive activity. meala6 -环孢素A的NMR构象。MeBmt-1、MeLeu-9和MeLeu-10残基侧链取向与免疫抑制活性的关系

International journal of peptide and protein research Pub Date : 1991-05-01

P R Gooley, P L Durette, J Boger, I M Armitage

{"title":"Conformation of MeAla6-cyclosporin A by NMR. Relationship of sidechain orientation of the MeBmt-1, MeLeu-9, and MeLeu-10 residues to immunosuppressive activity.","authors":"P R Gooley, P L Durette, J Boger, I M Armitage","doi":"","DOIUrl":"","url":null,"abstract":"MeAla6-cyclosporin A (MeAla6-CsA) is a unique CsA analog that shows weak immunosuppressive activity and yet binds strongly to the proposed cytosolic protein receptor, cyclophilin (CyP). Preliminary 1H NMR data showed significant chemical shift differences between spectra of MeAla6-CsA and CsA, suggesting different preferred conformations. A more detailed study, however, revealed that the backbone conformations of the two molecules are essentially identical, and that the differences can be accounted for, principally, by the sidechain motions of the MeBmt-1, MeLeu-9, and -10 residues. ROE and coupling constant data show that in MeAla6-CsA, the preferred chi 1 rotamers for MeLeu-9 and -10 are + 180 degrees (T), whereas in CsA there is a more even distribution of rotamer populations for MeLeu-10, and a preferred -60 degrees (G-) chi 1 rotamer for MeLeu-9. Similar data argue that the sidechain of MeBmt-1 is more restricted in its motion in MeAla-CsA than in CsA. Temperature studies suggest that these preferred rotamers for MeAla6-CsA may increase the stability of the hydrogen bond between NH(7) and CO(11), but prevent particular residues, especially the essential MeBmt-1 sidechain, from adopting orientations required to elicit immunosuppressive activity. The significant changes observed in the preferred orientations for the sidechains of the MeBmt-1, MeLeu-9, and MeLeu-10 residues in MeAla6-CsA argue that the particular orientations which they assume in CsA are not essential for cyclophilin binding.","PeriodicalId":14204,"journal":{"name":"International journal of peptide and protein research","volume":"37 5","pages":"351-63"},"PeriodicalIF":0.0,"publicationDate":"1991-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13077958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Heterodetic bicyclic decapeptide cyclo (Glu1-Leu2-Pro3-Gly4-Ser5-Ile6-Pro7- Ala8) cyclo-(1 gamma-5 beta) Phe9-Gly10. Synthesis and 2-D NMR conformational analysis. 异位双环十肽环(Glu1-Leu2-Pro3-Gly4-Ser5-Ile6-Pro7- Ala8)环-(1 γ -5 β) Phe9-Gly10。合成及二维核磁共振构象分析。

International journal of peptide and protein research Pub Date : 1991-05-01

G Barbato, G D'Auria, L Paolillo, G Zanotti

引用次数: 0

Human recombinant CuZn-superoxide dismutase. Amino acid sequence and location of the disulfide bond. 人重组cuzn -超氧化物歧化酶。二硫键的氨基酸序列和位置。

International journal of peptide and protein research Pub Date : 1991-02-01

M Peretz, M U Werber, Y Burstein

引用次数: 0

Fully synthetic immunogens. Part III. Synthesis of hinge-peptide/gastrin conjugates and their immunological properties. 全合成免疫原。第三部分。铰链肽/胃泌素缀合物的合成及其免疫学性质。

International journal of peptide and protein research Pub Date : 1991-02-01

E Wünsch, L Moroder, G Hübener, H J Musiol, R Von Grünigen, W Göhring, R Scharf, C H Schneider

{"title":"Fully synthetic immunogens. Part III. Synthesis of hinge-peptide/gastrin conjugates and their immunological properties.","authors":"E Wünsch, L Moroder, G Hübener, H J Musiol, R Von Grünigen, W Göhring, R Scharf, C H Schneider","doi":"","DOIUrl":"","url":null,"abstract":"As core molecule for the multiple attachment of antigenic peptides we have selected the human IgG1 hinge fragment 225-232/225'-232'. Two types of conjugates of this double-chain bis-cystinyl hinge-peptide were prepared i) by linking its C-termini to [NIe15]-human-little-gastrin-[2,17] and ii) by elongating the resulting hinge-peptide/[NIe15]-little-gastrin-[2-17] conjugate at the two N-termini with the human big-gastrin sequence 1-14 to produce the big-gastrin-[1-14]/hinge-peptide/little-gastrin-[2-17] conjugate. For the synthesis of these peptide structures both the route via the preformed double-chain bis-cystinyl peptide and the route via suitably protected monomeric bis-cysteinyl peptides were used. For the latter approach advantage was taken of the previous observation about the preferred oxidation of the bis-cysteinyl hinge-peptide 225-232 to the dimer in parallel alignment. Both synthetic routes led to identical products. Immunization experiments in guinea pigs with the synthetic hybrids led to surprisingly strong immune responses with anti-little-gastrin antibody titers comparable to those induced by the iso-1-cytochrome c/little-gastrin-[2-17] conjugate as carrier-hapten system. These findings show that the two gastrin constructs are fully competent immunogens. Additionally, the gastrin receptor-like specificity of the antibodies indicates that both the synthetic hybrids and the cytochrome c conjugate allow for expression of a little-gastrin-specific conformational epitope similar to the bioactive structure of this hormone. The usefulness of such synthetic hybrids is further confirmed by the observation that the bivalent immunogen, containing both the little-gastrin 2-17 and the big-gastrin 1-14 sequence, is capable of inducing an immune response against both antigenic sequences, although with different efficiency. These results fully confirm our expectations.","PeriodicalId":14204,"journal":{"name":"International journal of peptide and protein research","volume":"37 2","pages":"90-102"},"PeriodicalIF":0.0,"publicationDate":"1991-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12872851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Peptides containing 2-aminopimelic acid. Synthesis and study of in vitro effects on bacterial cells. 含有2-氨基苯甲酸的肽。体外对细菌细胞影响的合成与研究。

International journal of peptide and protein research Pub Date : 1991-02-01

P Le Roux, D Blanot, D Mengin-Lecreulx, J Van Heijenoort

引用次数: 0

Solid-phase synthesis of neurokinin A antagonists. Comparison of the Boc and Fmoc methods. 神经激肽A拮抗剂的固相合成。Boc和Fmoc方法的比较。

International journal of peptide and protein research Pub Date : 1991-02-01

P Rovero, L Quartara, G Fabbri

{"title":"Solid-phase synthesis of neurokinin A antagonists. Comparison of the Boc and Fmoc methods.","authors":"P Rovero, L Quartara, G Fabbri","doi":"","DOIUrl":"","url":null,"abstract":"During the preparation of the NK-2 selective tachykinin antagonist MEN 10208 (Thr-Asp-Tyr-D-Trp-Val-D-Trp-D-Trp-Arg-NH2) and its analogs by the solid-phase method employing the Boc strategy routinely used in our laboratory, we encountered difficulties in the coupling of hydrophobic amino acids D-Trp and Val. To study the coupling problems several syntheses of MEN 10208 and analogs were carried out with different activation strategies. These syntheses yielded considerable amounts of deletion sequences even though a negative Kaiser test was obtained after each coupling. Inaccessibility of the free amino group of the growing peptide due to steric hindrance of the hydrophobic residues during coupling, and for the ninhydrin complex during the Kaiser test, may account, at least in part, for the unsatisfactory synthetics results and for the false-negative ninhydrin tests. Repetition of each synthesis with the Fmoc strategy on a newly developed DOD resin for peptide amides using the DCC/HOBt chemistry gave superior results in terms of the yield and purity of the crude peptides. Therefore, the Fmoc strategy appears to offer advantages over the Boc method for the preparation of these peptides containing hydrophobic amino acids.","PeriodicalId":14204,"journal":{"name":"International journal of peptide and protein research","volume":"37 2","pages":"140-4"},"PeriodicalIF":0.0,"publicationDate":"1991-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13010938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0