Rezabal E, Marino T, Mercero J M, Russo N, Ugalde J M
Kimika Fakultatea, Euskal Herriko Unibertsitatea and Donostia International Physics Center, PK 1072, 20080 Donostia, Euskadi, Spain.
Inorg Chem. 2007 Aug 6;46(16):6413-9. doi: 10.1021/ic7004776. Epub 2007 Jul 3.
The coordination properties of three natural aromatic amino acids (AAAs)-phenylalanine (Phe), tyrosine (Tyr), and tryptophan (Trp)-to AlIII are studied in this work, devoting special attention to the role of the aromatic side chain. A comparison with aluminum(III)-alanine complexes is also presented. The polarizability arising from the ring has been seen to be a key factor in the stability of the complexes, with the order being Trp-AlIII > Tyr-AlIII > Phe-AlIII, starting from the most stable one. Cation-pi interactions between the metal and the aromatic ring are present in the lowest energy conformers, especially for Trp, which seems to be very well suited for these kinds of interactions, occurring with both the six- and five-membered rings of the indole side chain. The most stable coordination mode for the three AAAs is found to be tricoordinated with the N and O of the backbone chain and the aromatic ring, as was found theoretically and experimentally for other metals.
本文研究了三种天然芳香族氨基酸(AAA)——苯丙氨酸(Phe)、酪氨酸(Tyr)和色氨酸(Trp)与AlIII的配位性质,特别关注芳香侧链的作用。同时还给出了与铝(III)-丙氨酸配合物的比较。已发现由环产生的极化率是配合物稳定性的关键因素,从最稳定的配合物开始,顺序为Trp-AlIII > Tyr-AlIII > Phe-AlIII。金属与芳香环之间的阳离子-π相互作用存在于能量最低的构象中,特别是对于Trp,它似乎非常适合这类相互作用,吲哚侧链的六元环和五元环均可发生这种作用。发现这三种AAA最稳定的配位模式是通过主链的N和O以及芳香环进行三配位,这与其他金属在理论和实验上的发现一致。