Structurally Homologous Toxins Isolated from the Taiwan Cobra (Naja naja atra) Differ Significantly in Their Structural Stability

• Published in: Archives of biochemistry and biophysics Vol. 363; no. 1; pp. 107 - 115
• Main Authors: Sivaraman, T., Kumar, T.K.S., Tu, Y.T., Peng, H.J., Yu, C.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.1999
• Subjects: Animals; Circular Dichroism; Cobra Cardiotoxin Proteins - chemistry; Cobra Neurotoxin Proteins - chemistry; denaturation; Elapid Venoms - chemistry; Elapidae; folding; Guanidine - pharmacology; Magnetic Resonance Spectroscopy; Models, Molecular; Protein Conformation - drug effects; Protein Denaturation; Spectrophotometry, Ultraviolet; stability; structure; Temperature; Time Factors; denaturation; structure; stability; folding
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1006/abbi.1998.1057

Cardiotoxin and neurotoxin analogues isolated from snake venom sources are highly homologous proteins (>50% homology) with similar three-dimensional structures but exhibit drastically different biological properties. In the present study, we compare the conformational stability of cardiotoxin analogue III (CTX III) and cobrotoxin (CBTX), a neurotoxin analogue, from the Taiwan cobra (Naja naja atra), using circular dichroism spectroscopy and hydrogen–deuterium (H/D) exchange techniques in conjunction with two-dimensional NMR methods. Contrary to expectations, it is found that CTX III and CBTX differ significantly in their structural stabilities. The three-dimensional structure of CBTX is less stable than that of CTX III. The amide protons of residues at the N- and C-terminal ends of the CTX III molecule are strongly protected against H/D exchange, implying that the terminal ends of the molecule are bridged together by significant numbers of hydrogen bonds. However, in CBTX, amide protons at the terminal ends of the molecule do not exhibit an significant protection against H/D exchange. Comparison of the protection factors of the various amide protons in CTX III and CBTX reveals that the extraordinary stability of CTX III stems from the strong network of interactions among the residues at the N- and C-terminal ends and also due to the tight and ordered packing of the nonpolar residues involved in the triple-stranded, anti-parallel, β-sheet segment of the molecule.