La bibliothèque de Fulvio Orsini : contributions à l'histoire des collections d'Italie et à l'étude de la Renaissance / Pierre de Nolhac

Collection : Bibliothèque de l'École des Hautes-Études. Sciences philologiques et historiques ; 74

Carte du cours du Danube : depuis Passau jusqu'à Lintz : De l'Inn depuis Wœrgl jusqu'à son confluent : De la Salza depuis Hallein jusqu'à son confluent : et de la grande route de Kufften à Salzbourg / Atelier de gravure sur pierre de Hellrigel

Échelle(s) : [ca 1:205 000]

Rossignols amoureux : extrait d'"Hippolyte et Aricie" / Rameau, comp. ; Leïla Ben Sedira, S ; Quintette [i.e.] instrumental Pierre Jamet. Psyché / Manuel de Falla, comp. ; Leïla Ben Sedira, S ; G. Crunelle, fl. ; P. Jamet, hrp

Comprend : Rossignols amoureux / Rameau, comp. ; Leïla Ben Sedira, S ; G. Crunelle, fl. ; P. Jamet, hrp ; Psyché / Manuel de Falla, comp. ; Leïla Ben Sedira, S ; Quintette [i.e.] instrumental Pierre Jamet

Beta(1)-selective agonist (-)-1-(3,4-dimethoxyphenetylamino)-3-(3,4-dihydroxy)-2-propanol [(-)-RO363] differentially interacts with key amino acids responsible for beta(1)-selective binding in resting and active states.

(-)-1-(3,4-Dimethoxyphenetylamino)-3-(3,4-dihydroxy)-2-propanol [(-)-RO363] is a highly selective beta(1)-adrenergic receptor (beta(1)AR) agonist. To study the binding site of beta(1)-selective agonist, chimeric beta(1)/beta(2)ARs and Ala-substituted beta(1)ARs were constructed. Several key residues of beta(1)AR [Leu(110) and Thr(117) in transmembrane domain (TMD) 2], and Phe(359) in TMD 7] were found to be responsible for beta(1)-selective binding of (-)-RO363, as determined by competitive binding. Based on these results, we built a three-dimensional model of the binding domain for (-)-RO363. The model indicated that TMD 2 and TMD 7 of beta(1)AR form a binding pocket; the methoxyphenyl group of N-substituent of (-)-RO363 seems to locate within the cavity surrounded by Leu(110), Thr(117), and Phe(359). The amino acids Leu(110) and Phe(359) interact with the phenyl ring of (-)-RO363, whereas Thr(117) forms hydrogen bond with the methoxy group of (-)-RO363. To examine the interaction of these residues with beta(1)AR in an active state, each of the amino acids was changed to Ala in a constitutively active (CA)-beta(1)AR mutant. The degree of decrease in the affinity of CA-beta(1)AR for (-)-RO363 was essentially the same as that of wild-type beta(1)AR when mutated at Leu(110) and Thr(117). However, the affinity was decreased in Ala-substituted mutant of Phe(359) compared with that of wild-type beta(1)AR. These results indicated that Leu(110) and Thr(117) are necessary for the initial binding of (-)-RO363 with beta(1)-selectivity, and interaction of Phe(359) with the N-substituent of (-)-RO363 in an active state is stronger than in the resting state.

Carte de France / dressée par Pierre Tardieu

Échelle(s) : [ca 1:2 128 000], échelle 10 myriamètres [= 4,7 cm]

Lettres d'"aristocrates" : la Révolution racontée par des correspondances privées : 1789-1794 ([Reprod.]) / [publ. par] Pierre de Vaissière

Collection : Les archives de la Révolution française ; 3.60