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由L-天冬氨酸和L-谷氨酸组成的神经肽的结构及金属离子结合位点的13C核磁共振研究

13C n.m.r. study of the structure and the metal ion binding sites of neuropeptides composed of L-Asp and L-Glu.

作者信息

Lannom H K, Dill K, Denarié M, LaCombe J M, Pavia A A

出版信息

Int J Pept Protein Res. 1986 Jul;28(1):67-78. doi: 10.1111/j.1399-3011.1986.tb03230.x.

Abstract

13C NMR spectral data are presented for a variety of possible neuropeptides composed of L-Asp, Ac-L-Asp, and L-Glu which contain alpha and beta peptide linkages. The data for the various compounds are compared to the data presented for Ac-Asp-Glu, a known neuropeptide, in order to gain structural information about the related compounds. Indications are that for compounds 1 and 5, the cis peptide bond configuration exists due to the interaction of zwitterionic species. This interaction appears to be eliminated when the beta peptide bonds are formed, as in the case of compounds 3 and 7. Spin-lattice relaxation times were used to confirm the structures. Electron-nuclear relaxation rates are also used to elucidate the metal ion binding sites of these species.

摘要

给出了由L-天冬氨酸、Ac-L-天冬氨酸和L-谷氨酸组成的多种可能的神经肽的13C NMR光谱数据,这些神经肽含有α和β肽键。将各种化合物的数据与已知神经肽Ac-Asp-Glu的数据进行比较,以便获得有关相关化合物的结构信息。有迹象表明,对于化合物1和5,由于两性离子物种的相互作用,存在顺式肽键构型。当形成β肽键时,如化合物3和7的情况,这种相互作用似乎被消除了。自旋晶格弛豫时间用于确认结构。电子-核弛豫率也用于阐明这些物种的金属离子结合位点。

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