首页> 外文期刊>Biochemistry >Fidelity of binding of the guanidinium nucleic acid (DNG) d(Tg)4-T-azido with short strand DNA oligomers (A5G3A5, GA4G3A4G, G2A3G3A3G2, G2A2G5A2G2). A kinetic and thermodynamic study.
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Fidelity of binding of the guanidinium nucleic acid (DNG) d(Tg)4-T-azido with short strand DNA oligomers (A5G3A5, GA4G3A4G, G2A3G3A3G2, G2A2G5A2G2). A kinetic and thermodynamic study.

机译:胍基核酸(DNG)d(Tg)4-T-叠氮基与短链DNA寡聚物(A5G3A5,GA4G3A4G,G2A3G3A3G2,G2A2G5A2G2)的结合保真度。动力学和热力学研究。

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摘要

Short strand DNA oligomers (A5G3A5, GA4G3A4G, G2A3G3A3G2, and G2A2G5A2G2) and the guanidinium (g) linked thymidyl nucleoside d(Tg)4-T-azido associate as triplexes. The melting temperatures, Tm, the association and dissociation kinetic and thermodynamic parameters and activation energies for the triplexes were determined by UV thermal analysis. The hypochromic shift and Tm for triplex formation increases with increase in concentration and decreases with the number of mismatches. The melting temperatures are between 35 and 55 degrees C in the range of ionic strength of 0.06-0.24 and decrease with increase in ionic strength at 100 deg/(ionic strength unit). The melting and cooling curves exhibit hysteresis behavior in the temperature range 5-95 degrees C at 0.2 deg/min thermal rate. From these curves, the rate constants and the energies of activation for association (k(on), E(on)) and dissociation (k(off), E(off)) processes were obtained. The second-order rate constants, k(on), for the triplex formation at 288 K are between 10 and 500 M(-2) s(-1). Values of k(on) increase with the decrease in the ionic strength. The first order rate constants for the dissociation, k(off), at 288 K are between 10(-6) and 40 x 10(-6) s(-1) and increase with increase in ionic strength. The energies of activation for the association and dissociation processes are in the range -22 to -9 kcal/mol and 8 to 29 kcal/mol, respectively. At 6.3 x 10(-5) M/base and at the physiological ionic strength (0.15-0.30) and below, the triplex structures formed with d(Tg)4-T-azido and A5G3A5 and GA4G3A4G have well-defined Tm values. The melting curves with G2A3G3A3G2 and G2A2G5A2G2 are very shallow with small hypochromic shifts denoting negligible binding at physiological ionic strength. Therefore, with the increase in the G content (mismatched base pairs) at a certain concentration (e.g., 6.3 x 10(-5) M/base), discrimination (change in fidelity) occurs in the formation and strength of binding of d(Tg)4-T-azido to d(pAn pGm) oligomers. The standard molar enthalpies for triplex formation have in general larger negative values at low ionic strength than at high ionic strength, indicating that at lower mu values the formation of triplexes of d(Tg)4-T-azido with d(pAn pGm) are more favorable. The values of deltaH(standard)(288) calculated from the activation parameters are between -17 and -49 kcal/mol, and the values of deltaG(standard)(288) are between -7.5 and -11.8 kcal/mol for A5G3A5, GA4G3A4G, G2A3G3A3G2, and G2A2G5A2G2, respectively. There is a linear relationship in the enthalpy-entropy compensation for the triplex melting thermodynamics.
机译:短链DNA寡聚物(A5G3A5,GA4G3A4G,G2A3G3A3G2和G2A2G5A2G2)和胍基(g)连接的胸苷核苷d(Tg)4-T-叠氮基缔合为三链体。通过UV热分析确定三重链的熔融温度Tm,缔合和解离动力学和热力学参数以及活化能。三重态形成的变色位移和Tm随着浓度的增加而增加,并且随着错配的数量而减少。熔融温度在离子强度为0.06-0.24的范围内在35至55℃之间,并且随着在100℃/(离子强度单位)下离子强度的增加而降低。熔化和冷却曲线在5-95摄氏度的温度范围内以0.2度/分钟的热速率显示出滞后行为。从这些曲线,获得了速率常数和缔合(k(on),E(on))和离解(k(off),E(off))过程的活化能。在288 K下形成三重态的二阶速率常数k(on)在10到500 M(-2)s(-1)之间。 k(on)的值随离子强度的降低而增加。在288 K时解离的一级速率常数k(off)在10(-6)和40 x 10(-6)s(-1)之间,并且随着离子强度的增加而增加。用于缔合和解离过程的活化能分别在-22至-9kcal / mol和8至29kcal / mol的范围内。在6.3 x 10(-5)M /碱基和生理离子强度(0.15-0.30)及以下时,由d(Tg)4-T-叠氮基和A5G3A5和GA4G3A4G形成的三链体结构具有明确的Tm值。 G2A3G3A3G2和G2A2G5A2G2的熔解曲线非常浅,具有小的变色移位,表示在生理离子强度下的结合可忽略不计。因此,随着一定浓度(例如6.3 x 10(-5)M /碱基)的G含量(不匹配的碱基对)的增加,在d( Tg)4-T-叠氮基到d(pAn pGm)低聚物。低离子强度下的三摩尔形成标准摩尔焓通常比高离子强度下具有更大的负值,表明在较低的mu值下,具有d(pAn pGm)的d(Tg)4-T-叠氮基三重结构的形成为更有利。根据激活参数计算得出的deltaH(standard)(288)值在-17和-49 kcal / mol之间,对于A5G3A5,deltaG(standard)(288)的值在-7.5和-11.8 kcal / mol之间, GA4G3A4G,G2A3G3A3G2和G2A2G5A2G2。三重熔化热力学的焓-熵补偿具有线性关系。

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