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一种自互补核糖寡核苷酸A7U7螺旋-线圈转变的弛豫动力学

Relaxation kinetics of the helix-coil transition of a self-complementary ribo-oligonucleotide: A7U7.

作者信息

Breslauer K J, Bina-Stein M

出版信息

Biophys Chem. 1977 Nov;7(3):211-6. doi: 10.1016/0301-4622(77)87024-5.

Abstract

Relaxation measurements on the kinetics of the double helix to coil transition for the self-complementary ribo-oligonucleotide A7U7 are reported over a concentration range of 6.9 micrometer to 19.6 micrometer in single strand in 1 M NaCl. The rate constants for helix formation are about 2 X 10(6) M-1 s-1 and decrease with increasing temperature yielding an activation enthalpy of -6 kcal/mole. The rate constants for helix dissociation range from 3 to 250 s-1 and increase with increasing temperature yielding an activation enthalpy of +45 kcal/mole. The kinetic data reported here for 1 M NaCl is compared with previously published results obtained at lower salt concentrations. These data are discussed in terms of the quantitative effect of ionic strength on the kinetics of helix-coil transitions in oligo- and polynucleotides.

摘要

报道了在1M NaCl中,对自互补核糖寡核苷酸A7U7从双螺旋到单链卷曲转变动力学的弛豫测量,单链浓度范围为6.9微米至19.6微米。螺旋形成的速率常数约为2×10⁶M⁻¹ s⁻¹,并随温度升高而降低,活化焓为-6千卡/摩尔。螺旋解离的速率常数范围为3至250 s⁻¹,并随温度升高而增加,活化焓为+45千卡/摩尔。本文报道的1M NaCl的动力学数据与先前在较低盐浓度下发表的结果进行了比较。根据离子强度对寡核苷酸和多核苷酸中螺旋-卷曲转变动力学的定量影响对这些数据进行了讨论。

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