Freist W, Sternbach H, Cramer F
Max-Planck-Institut für experimentelle Medizin, Göttingen, Germany.
Eur J Biochem. 1996 Sep 15;240(3):526-31. doi: 10.1111/j.1432-1033.1996.0526h.x.
For discrimination between phenylalanine and 18 other naturally occurring non-cognate amino acids by the class II aminoacyl-tRNA synthetase specific for phenylalanine, discrimination factors, D, of 190-6300 have been determined from kcal and K(m) values. Generally, phenylalanyl-tRNA synthetase is more specific than the class II enzymes specific for Lys and Thr, but works with lower accuracy than the class I enzymes specific for IIe, Tyr, and Arg. In aminoacylation of tRNA(Phe)-C-C-A(3'NH2) discrimination factors D1 vary between 80-1610. Pre-transfer proof-reading factors II1 are in the range 2.3-74, post-transfer proof-reading factors II2 in the range 1.0-4.6, showing that pre-transfer proof-reading is the main correction step, post-transfer proofreading is less effective or negligible. Initial discrimination factors (I1 and I2) caused by differences in Gibbs free energies of binding between phenylalanine and non-cognate amino acids have been calculated assuming a two-step binding process. Factors I1 can be related to hydrophobic-interaction forces depending on accessible surface areas of the amino acids, factors I2 scatter about a low mean value and do not show any relation to amino acid structures or surfaces, indicating less checking of amino acid side chains in the putative second binding step.
对于由苯丙氨酸特异性的II类氨酰 - tRNA合成酶区分苯丙氨酸与其他18种天然存在的非同源氨基酸,已根据kcat和Km值确定了190 - 6300的区分因子D。一般来说,苯丙氨酰 - tRNA合成酶比赖氨酸和苏氨酸特异性的II类酶更具特异性,但与异亮氨酸、酪氨酸和精氨酸特异性的I类酶相比,其准确性较低。在tRNA(Phe)-C-C-A(3'NH2)的氨酰化过程中,区分因子D1在80 - 1610之间变化。转移前校对因子II1在2.3 - 74范围内,转移后校对因子II2在1.0 - 4.6范围内,这表明转移前校对是主要的校正步骤,转移后校对效果较差或可忽略不计。假设存在两步结合过程,已计算出由苯丙氨酸与非同源氨基酸结合的吉布斯自由能差异引起的初始区分因子(I1和I2)。因子I1可能与取决于氨基酸可及表面积的疏水相互作用力有关,因子I2围绕一个低平均值分散,并且与氨基酸结构或表面没有任何关系,这表明在假定的第二步结合中对氨基酸侧链的检查较少。