Centro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC), Universidad Nacional de Córdoba - Consejo Nacional de Investigaciones Científicas y Técnicas (UNC-CONICET), Departamento de Química Biológica Ranwel Caputto, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Haya de la Torre s/n, X5000HUA, Córdoba, Pabellón Argentina Ala Oeste, Argentina.
Arch Biochem Biophys. 2020 Aug 15;689:108473. doi: 10.1016/j.abb.2020.108473. Epub 2020 Jun 22.
Eleven missense mutations have been describe in human triosephosphate isomerase (TPI), affecting its catalytic function. Several of these mutations generate triosephosphate isomerase deficiency, the consequences of which can in some cases be lethal. The missense F240L mutation was found in a Hungarian patient showing symptoms of chronic hemolytic anemia and neuromuscular dysfunction. In vitro studies using a recombinant version of this mutant showed that it affects kinetic parameters, thermal stability and dimeric stability. Using X-ray crystal structures, the present paper describes how this mutation affected the flexibility of catalytic residues K13 and part of the (β/α) 8-barrel fold facing the dimeric interface in the TPI.
已在人体磷酸丙糖异构酶(TPI)中描述了 11 种错义突变,这些突变影响其催化功能。其中一些突变会导致磷酸丙糖异构酶缺乏,在某些情况下,其后果可能是致命的。错义 F240L 突变在一名表现出慢性溶血性贫血和神经肌肉功能障碍症状的匈牙利患者中发现。使用该突变体的重组版本进行的体外研究表明,它会影响动力学参数、热稳定性和二聚体稳定性。本文利用 X 射线晶体结构,描述了该突变如何影响催化残基 K13 的灵活性,以及面向 TPI 二聚体界面的(β/α)8 桶折叠的一部分。