Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Robert Schwyzer"'
Publikováno v:
Journal of Peptide Science. 3:65-81
Lipid-induced secondary structures and orientations of the two enantiomeric [Leu5]-enkephalins, L-Tyr-Gly-Gly- L-Phe-L-Leu, and D-Tyr-Gly-Gly-D-Phe- D-Leu, on flat multi-bilayers of 1-palmitoyl-2-oleoyl-sn- glycero-3-phosphocholine (POPC) were examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37a6d2b4907d77896ddc540485f95abd
https://doi.org/10.1002/(sici)1099-1387(199701)3:1<65::aid-psc90>3.0.co
https://doi.org/10.1002/(sici)1099-1387(199701)3:1<65::aid-psc90>3.0.co
Autor:
Robert Schwyzer
Publikováno v:
Journal of Molecular Recognition. 8:3-8
Conformations of regulatory peptides interacting with artificial lipid membranes were compared with those of chemically constrained molecules that react selectively with different receptor classes. Striking similarities in the topochemistry of molecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90d7d0f1b5ce1fe22b64205c7b734dd8
https://doi.org/10.1002/jmr.300080103
https://doi.org/10.1002/jmr.300080103
Autor:
Robert Schwyzer
Publikováno v:
Biopolymers. 37:5-16
The ideas developed in the Membrane Compartments Theory which allow a quantitative prediction of receptor preference are discussed in terms of our present knowledge of opioid and neurokinin receptor structure. Furthermore, conformations of regulatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::660b5384de948e1a8577903d91999f05
https://doi.org/10.1002/bip.360370104
https://doi.org/10.1002/bip.360370104
Autor:
Robert Schwyzer
Publikováno v:
Biopolymers. 31:785-792
Ideas about “active conformations” of peptides as the basis of their biological action are reviewed and put into perspective with recent work on the possible role of the lipid phase of the target cell membrane in mediating receptor subtype select
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd5b736fe489911843e8b63b93dcb66
https://doi.org/10.1002/bip.360310624
https://doi.org/10.1002/bip.360310624
Publikováno v:
International journal of peptide and protein research. 39(5)
The enhancement of fluorescence emission from the tryptophan residue of glucagon, the quenching of that emission with acrylamide and with 5-doxyl and 16-doxyl stearic acid, circular dichroism spectra, the release of 6-carboxyfluorescein, and polarize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9552d8872bfc41cffdf33336f3258a88
https://pubmed.ncbi.nlm.nih.gov/1358848
https://pubmed.ncbi.nlm.nih.gov/1358848
Publikováno v:
Peptides ISBN: 9789401050050
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7588f77656ee76331654e3870ab6a55a
https://doi.org/10.1007/978-94-011-2264-1_59
https://doi.org/10.1007/978-94-011-2264-1_59
Autor:
Robert Schwyzer
Publikováno v:
Journal of receptor research. 11(1-4)
In this review, I discuss our recent work on the possible role of the lipid phase of the target cell membrane in mediating receptor subtype selectivity of peptides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f61442b815a80f3db297e2106773f1
https://pubmed.ncbi.nlm.nih.gov/1653346
https://pubmed.ncbi.nlm.nih.gov/1653346
Autor:
Aung Tun‐Kyi, Robert Schwyzer
Publikováno v:
Helvetica Chimica Acta. 59:1642-1646
The preparation and properties of thirty two N(α)-[2-(p-phenylazophenyl)-isopropylcarbonyl]-amino-acids and derivatives are described. The new coloured protecting group (AZOC-) can be easily and selectively removed with mild acid treatment, much the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ab3ac36e1ebfaf6324b6637e7661af
https://doi.org/10.1002/hlca.19760590524
https://doi.org/10.1002/hlca.19760590524
Publikováno v:
Helvetica Chimica Acta. 62:2442-2451
Alkali cation complexation and bilayer transport by the bicyclic decapeptides S,S′-bis-cyclo-glycyl-L-hemicystyl-glycyl-glycyl-L-prolyl (1), S, S′-bis-cyclo-glycyl-L-hemicystyl-glycyl-glycyl-D-prolyl (2), S, S′-bis-cyclo-glycyl-L- hemicystyl-sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72f9ae39381776920972be2e335bcb35
https://doi.org/10.1002/hlca.19790620739
https://doi.org/10.1002/hlca.19790620739