Kawasaki Maki, Oda Masayuki
Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto 606-8522, Japan.
Biophys Physicobiol. 2021 Mar 25;18:78-84. doi: 10.2142/biophysico.bppb-v18.009. eCollection 2021.
The minimum DNA-binding domain of the transcrip-tional factor c-Myb R2R3 remarkably fluctuates in the solution. In the present study, we evaluated the protein fluctuation of R2R3 C130I mutant, R2R3*, on its DNA-binding and folding thermodynamics. DNA-binding analysis using isothermal titration calorimetry revealed that the heat capacity change determined from the correlation between temperature and binding enthalpy change is highly negative above 35°C, indicating that the fluctuation increases with increasing temperature and elevates the conformational change on DNA binding. The results were in accordance with those of differential scanning calorimetry, which revealed that the heat capacity corresponding to thermal denatu-ration gradually increased above 35°C, followed by the broad transition peak. In contrast, the transition peak of R2R3* in the DNA-bound state was sharper and larger than that in the DNA-unbound state. The fluctuating form could transform into lesser fluctuating form upon DNA binding, resulting in a larger enthalpy change for denaturation of R2R3* in the DNA-bound state. It should also be noted that R2R3* could specifi-cally bind to DNA around thermal denaturation temperature. This would be due to proteins with numerous fluctuations. Moreover, we discuss specific and non-specific DNA binding accompanied by the conformational change between well-ordered and disordered forms of R2R3* observed around the denaturation temperature.
转录因子c-Myb R2R3的最小DNA结合结构域在溶液中显著波动。在本研究中,我们评估了R2R3 C130I突变体R2R3在其DNA结合和折叠热力学方面的蛋白质波动情况。使用等温滴定量热法进行的DNA结合分析表明,根据温度与结合焓变之间的相关性确定的热容变化在35°C以上高度为负,这表明波动随温度升高而增加,并提高了DNA结合时的构象变化。这些结果与差示扫描量热法的结果一致,差示扫描量热法表明,对应于热变性的热容在35°C以上逐渐增加,随后出现宽的转变峰。相比之下,R2R3在DNA结合状态下的转变峰比在DNA未结合状态下更尖锐、更大。波动形式在DNA结合时可转变为波动较小的形式,导致DNA结合状态下R2R3变性的焓变更大。还应注意的是,R2R3在热变性温度附近可特异性结合DNA。这可能是由于蛋白质具有大量波动。此外,我们讨论了在变性温度附近观察到的R2R3*有序和无序形式之间的构象变化所伴随的特异性和非特异性DNA结合。