Burckhardt G, Walter A, Zimmer C
Abteilung Molekulare Biologie, Institut fur Molekularbiologie der Friedrich-Schiller-Universitat Jena, Germany.
J Biomol Struct Dyn. 1996 Feb;13(4):671-6. doi: 10.1080/07391102.1996.10508879.
Poly(dA-dT) center dot poly(dA-dT) which adopts the Z-form at 5 M NaCl in presence of 95 mM Ni2+ions is reversed to the B-conformation by the nonintercalating drugs netropsin (Nt) and distamycin A (Dst). The drug-induced reversal from the Z-to B-form of poly(dA-dT) center dot poly(dA-dT) is evidenced by CD spectral changes at characteristic wavelengths around 295 nm and 248 nm. The drug-induced conformational transition is accompanied by a slow kinetic process. The results suggest the preference of these AT-specific drugs for the B-form and the inability of Nt and Dst to form a stable complex with the Z-form of poly(dA-dT) center dot poly(dA-dT).
在95 mM Ni²⁺离子存在下于5 M NaCl中呈Z型的聚(dA-dT)·聚(dA-dT),会被非嵌入性药物纺锤菌素(Nt)和偏端霉素A(Dst)转变为B构象。聚(dA-dT)·聚(dA-dT)从Z型到B型的药物诱导转变,通过295 nm和248 nm左右特征波长处的圆二色光谱变化得到证实。药物诱导的构象转变伴随着一个缓慢的动力学过程。结果表明这些AT特异性药物对B型的偏好,以及Nt和Dst无法与聚(dA-dT)·聚(dA-dT)的Z型形成稳定复合物。