Kwak Juliann, De Capua Antonia, Locardi Elsa, Goodman Murray
Department of Chemistry and Biochemistry, University of California-San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0343, USA.
J Am Chem Soc. 2002 Nov 27;124(47):14085-91. doi: 10.1021/ja0209621.
A new scaffold, TREN-(suc-OH)(3) where TREN is tris(2-aminoethyl)amine and suc is the succinic acid spacers, was incorporated to assemble triple helices composed of Gly-Nleu-Pro sequences (Nleu denotes N-isobutylglycine). Extensive biophysical studies which include denaturation studies, CD and NMR spectroscopy, and molecular modeling demonstrated that TREN-suc-(Gly-Nleu-Pro)(n)-NH(2) (n = 5 and 6) form stable triple helical structures in solution. A comparative analysis of TREN-assembled and KTA-assembled collagen mimetics (KTA denotes Kemp triacid, 1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid) indicates that the flexibility of the TREN scaffold is superior to the KTA scaffold in inducing triple helicity. This effect most likely arises from the flexibility of the TREN scaffold which allows the three peptide chains to adjust their register for a tighter triple helical packing.
一种新的支架TREN-(suc-OH)(3)(其中TREN是三(2-氨基乙基)胺,suc是琥珀酸间隔基)被用于组装由Gly-Nleu-Pro序列(Nleu表示N-异丁基甘氨酸)组成的三螺旋。包括变性研究、圆二色光谱和核磁共振光谱以及分子建模在内的广泛生物物理研究表明,TREN-suc-(Gly-Nleu-Pro)(n)-NH(2)(n = 5和6)在溶液中形成稳定的三螺旋结构。对TREN组装的和KTA组装的胶原模拟物(KTA表示肯普三酸,1,3,5-三甲基环己烷-1,3,5-三羧酸)的比较分析表明,在诱导三螺旋性方面,TREN支架的灵活性优于KTA支架。这种效应很可能源于TREN支架的灵活性,它允许三条肽链调整其排列以实现更紧密的三螺旋堆积。