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  • 1
    Electronic Resource
    Electronic Resource
    Circular dichroism and structure of Schiff's bases of hydroxybenzaldehydes anchored to poly(L-lysine) and poly(L-α,γ-diaminobutyric acid) (1978)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 1041-1049 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Schiff's bases of ortho-, meta- and para-hydroxybenzaldehydes with poly(L-α,γ-diaminobutyric acid) and poly(L-lysine) were investigated in solution of methanol and methanol-water mixtures by circular dichtroism, absorption spectroscopy and equilibrium dialysis techniques. The results so far obtained allow us to propose a molecular model, which fully justifies the stereospecific binding of ortho-hydroxybenzaldehyde with the polypeptide chain; moreover it is able to explain the dramatic change of the chemical equilibrium in the hydrolysis reaction.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1978.021790418
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  • 2
    Electronic Resource
    Electronic Resource
    Chromatographic fractionation of primary amine initiated poly-γ-benzyl-L-glutamate (1966)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 97 (1966), S. 113-127 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die SCHULZsche Theorie über die chromatographische Fraktionierung mittels BAKERWILLIAMS-Säulen wurde auf das System Poly-γ-benzyl-L-glutamat/Methanol/Methylenchlorid angewandt.Es wurde gefunden, daß die Trennung sehr wirksam ist, wenn die Fraktionierungsbedingungen sorgfältig ausgewählt werden. Darüber hinaus stimmen die Ergebnisse mit dem vermuteten Mechanismus der mit primären Aminen initiierten N-Carboxyanhydrid-(NCA)-Polymerisation gut überein. An den Ergebnissen der Fraktionierung wurde erkannt, daß das Zahlenmittel des Polymerisationsgrades P̄n annähernd dem Verhältnis der Monomeranfangskonzentration zur Initiatorkonzentration ([M]0/[I]0) gleich ist. Eine sehr große Uneinheitlichkeit wurde mit P̄w/P̄n ≃ 7 in Übereinstimmung mit älteren Literaturdaten gefunden1.
    Notes: The SCHULZ theory on the chromatographic fractionation with a BAKER and WILLIAMS column was applied to the system poly-γ-benzyl-L-glutamate/methanol/methylenechloride.It was found that the separation is very efficient if the fractionation conditions are carefully selected. Moreover the results are in good agreement with the suggested mechanism of N-carboxyanhydride (NCA) polymerization initiated by primary amines. In fact from the fractionation data it was found that the number average degree of polymerization P̄n is approximatively equal to the ratio between the initial concentrations of monomer and initiator ([M]0/[I]0). A very large inhomogeneity was found with P̄w/P̄n ≃ 7, in agreement with previous literature data1.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1966.020970110
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  • 3
    Electronic Resource
    Electronic Resource
    Formation, properties and structures of bis (o-hydroxybenzylideneamine)copper(II) chelates of polypeptide ligands (1974)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 175 (1974), S. 327-337 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Es wurden die Bildung, die optischen Eigenschaften und die Strukturen der Bis(o-hydroxybenzylidenamin)Kupfer(II)-Chelate von Poly(L-lysin), Poly(L-ornithin) und Poly(L-α,γ-diaminobuttersäure) untersucht.Aus den Versuchsergebnissen ging hervor, daß diese Polykomplexe in alkoholisch wäßriger Lösung eine bestimmte Struktur besitzen. Aus den strukturellen Eigenschaften resultierte, daß die asymmetrischen Polypeptid-Ketten die Metall-Chelate stereospezifisch binden.Auf Grund dieser Ergebnisse kann man stereoselektive Reaktionen der Kupfer(II)-polykomplexe von Bis(o-hydroxybenzylidenamin) erwarten.
    Notes: Formation, optical properties and structures of bis(o-hydroxybenzylideneamine)copper(II) chelates of poly(L-lysine), poly(L-ornithine), and poly(L-α,β-diaminobutyric acid) were investigated.Experimental evidence was obtained for a definite structure of these polycomplexes in alcoholic/aqueous solution. Structural features showed that asymmetric polypeptide matrices bind metal chelates stereospecifically. On the basis of these results stereoselective reactions on bis(o-hydroxybenzylideneamine)copper(II) polycomplexes are expected.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1974.021750201
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  • 4
    Electronic Resource
    Electronic Resource
    Fast atom bombardment mass spectrometry and selective acid hydrolysis for the analysis of partially modified retro-inverso peptide analogues (1989)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 18 (1989), S. 867-871 
    Details
    ISSN: 0887-6134
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fast atom bombardment (FAB) mass spectrometry has been successfully applied to the analysis of partially modified retro-inverso peptide isomers. The spectra are characterized by abundant protonated molecular ions and also by sequence ions due to fragmentation of the inverted bonds. Unambiguous information, as to the nature and the position in the backbone of the amino acids involved in the partial modification of the structure, are given by using a combination of FAB mass spectrometry and partial, selective acid hydrolysis, without separation of the resulting peptide mixtures.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200181005
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  • 5
    Electronic Resource
    Electronic Resource
    Analysis of a bioactive synthetic analogue of tuftsin by tandem mass spectrometry: Anomalous fast atom bombardment activated processes (1994)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 23 (1994), S. 262-266 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fast atom bombardment (FAB) tandem mass spectrometry has been used to analyse the biologically potent, partially modified retro-inverso (PMRI) synthetic isomer of tuftsin: this compound represents the active peptide of the fraction of γ-globulin (leukokinin) which binds specifically to blood neutrophilic leukocytes and monocytes. Protonated molecules and fragment ions were collisionally dissociated at low energies in a triple-quadrupole mass spectrometer to yield a complete picture of the reactions that occur in the condensed and in the gas phase. The study shows that, when retro-inversion is within the N-terminal amino acid, charge localization at the basic sites (possibly at the N-terminus) induces a marked decomposition of the molecule, the loss of ammonia being the most favourable fragmentation process. Also, artifacts are formed in the liquid phase via bimolecular reactions promoted by the high-energy beam. The findings indicate that despite the fact that PMRI isomers of this type are stable against exo-peptidases and also stable under acidic conditions, they appear to be labile under conditions where the energy deposition, due to FAB is necessarily high.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200230504
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  • 6
    Electronic Resource
    Electronic Resource
    1H-nmr studies of synthetic polypeptide models of Plasmodium falciparum circumsporozoite protein tandemly repeated sequence (1989)
    New York : Wiley-Blackwell
    Biopolymers 28 (1989), S. 225-246 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The major immunodominant region of the coating protein of Plasmodium falciparum sporozoites contains multiple tandem copies of the sequence Asn-Ala-Asn-Pro (NANP). Current efforts for the development of an antisporozoite vaccine are focused on the synthesis of polypeptides reproducing part of the circumsporozoite protein repeat sequence and, in an attempt to relate conformational properties and biological response, 1H-nmr one- and two-dimensional studies of the synthetic models (NANP)2NA and (NANP)6 were carried out in water and water/methanol mixtures, at 400 and 500 MHz. In water, (NANP)6 undergoes fast conformational averaging. At variance, in water/methanol, the molecule appears to adopt an extensive structure, but detailed analysis is impaired by high spectral degeneracy. Based on the results obtained with (NANP)2NA and from preliminary expermints in water/trifluoroethanol, an interpretation is suggested for the (NANP)6 data in water/methanol in terms of a mixed sequence of βI-turns and half-turns (or/and γI-turns) around the positions Ni-1-Pi-Ni+1.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360280124
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  • 7
    Electronic Resource
    Electronic Resource
    Toward the elucidation of the mechanism of attachment and entry of malaria sporozoites into cells: Synthetic polypeptides from the circumsporozoite protein of Plasmodium falciparumbind Ca2+ and interact with model phospholipid membranes (1991)
    New York : Wiley-Blackwell
    Biopolymers 31 (1991), S. 587-594 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Through the joint use of CD, Fourier transform ir (FTIR), and attenuated total reflectance FTIR we have found that synthetic polypeptide models of the Plasmodium falciparum circumsporozoite (CS) protein repeat domain bind calcium ions in helicogenic environments. Ca2+-(NANP)n complexes (n ≥ 20) interact vectorially with model phospholipid membranes orienting their polypeptide axes preferentially along those of the lipid acyl chains. It is proposed that the P. falciparum CS protein central region, rather than acting as a molecular lure helping the parasite to evade host immune control, plays, as a specific Ca2+ macroligand, a critical functional role during attachment, invasion, and development of the malaria parasite in the hepatic cell.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360310602
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  • 8
    Electronic Resource
    Electronic Resource
    Synthesis and circular dichroism characterization of L-azetidine-2-carboxylic acid cyclic peptidesThis is paper XX of the series “Cyclic Peptides.” For the previous paper in this series, see Baron et al. (1977) J. Am. Chem. Soc. 99, 8299-8306. (1978)
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2385-2399 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several cyclic hemopeptides containing L-azetidine-2-carboxylix acid (Aze) - an imino acid homologous with proline but containing one less methylene group in its cyclic side chain - have been prepared. The peptides reported include (Aze)2, cyclo(Aze)3, and cyclo(Aze)6. The synthesis and spectral characterization of these cyclic peptides are described, and the results discussed in terms of the rigidity and steric constraints attributable to Aze-containing peptides. CD spectra of these materials in several solvents are reported and compared with those of proline analogs; the similarity between the CD spectra of cyclo(Aze)3 and cyclo (Pro)3, is noted.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1978.360171008
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  • 9
    Electronic Resource
    Electronic Resource
    Conformational behavior of poly-N5-(3-hydroxypropyl)-L-glutamine in water-methanol mixtures studied by 13C nmr and CD spectroscopy (1974)
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 2209-2225 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The helix-coil transition of poly-N5-(3-hydroxypropyl)-L-glutamine (PHPLG) has been studied in methanol-water by CD and cmr spectroscopy. For polydisperse PHPLG, two separate peaks arising from residues in helical and random-coil conformations are observed during the transition for both main-chain carbons. These results are discussed and compared to those observed in the case of a polymer sample obtained by racemization of PHPLG in 0.1 M NaOH and of PHPLG samples of controlled molecular weight and dispersity. The dominant influence of the molecular-weight heterogeneity on the double-peak phenomenon has been verified. The linewidths and chemical shift of the 13C resonances are discussed in terms of side-chain-main-chain interactions and side-chain solvation.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1974.360131105
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  • 10
    Electronic Resource
    Electronic Resource
    13C Nmr study of the helix-coil transition of poly-N5-(3-hydroxypropyl)-L-glutamine (1974)
    New York : Wiley-Blackwell
    Biopolymers 13 (1974), S. 2405-2405 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1974.360131119
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