Sivaraman T, Kumar T K, Jayaraman G, Han C C, Yu C
Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan, Republic of China.
Biochem J. 1997 Jan 15;321 ( Pt 2)(Pt 2):457-64. doi: 10.1042/bj3210457.
Cardiotoxin analogue III (CTX III) is a low-molecular-mass all-beta-sheet protein isolated from the Taiwan cobra (Naja naja atra) venom. A stable partially structured state similar to the "molten globule' state has been identified for CTX III in a 3% (w/v) solution of 2,2,2-trichloroacetic acid at 298 K. This stable state has been structurally characterized using a variety of techniques such as CD, 1-anilinonaphthalene-8-sulphonate fluorescence binding, Fourier transform IR and two-dimensional NMR spectroscopy techniques. Direct assignment of the homonuclear two-dimensional NMR spectra of the protein in 3% trichloroacetic acid showed that drastic structural perturbation had not taken place in the protein and that the 'intermediate' state retained a significant portion of the native secondary-structural interactions. It is found that about 65% of the native beta-sheet structural contacts are maintained in the partially structured state of CTX III in 3% trichloroacetic acid.
心脏毒素类似物III(CTX III)是一种从台湾眼镜蛇(眼镜蛇)毒液中分离出的低分子量全β-折叠蛋白。在298 K的2,2,2-三氯乙酸3%(w/v)溶液中,已鉴定出CTX III存在一种类似于“熔球”状态的稳定部分结构化状态。使用多种技术,如圆二色光谱(CD)、1-苯胺基萘-8-磺酸盐荧光结合、傅里叶变换红外光谱和二维核磁共振光谱技术,对这种稳定状态进行了结构表征。对蛋白质在3%三氯乙酸中的同核二维核磁共振谱的直接归属表明,蛋白质中并未发生剧烈的结构扰动,且“中间”状态保留了相当一部分天然二级结构相互作用。研究发现,在3%三氯乙酸中,CTX III的部分结构化状态下约65%的天然β-折叠结构接触得以保留。