Sokolik C W, Liang T C, Wold F
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77225.
Protein Sci. 1994 Jan;3(1):126-31. doi: 10.1002/pro.5560030116.
In a continuing attempt to explore the types of specificity determinants that may affect protein-protein (peptide) interactions, a number of short (2-5 residues) acetylated peptides have been compared as substrates for the enzyme acetylaminoacyl-peptide hydrolase (EC 3.4.19.1). The reference substrate was Ac-AAAA, and most of the other substrates were derived from this basic structure by single amino acid substitutions. The Km and kcat for the different substrates were determined by standard steady-state kinetics, and the corresponding delta delta GT++ value derived from kcat/Km was used for the comparison, setting delta detal GT++ for Ac-AAAA equal to 0. The best substrates were found to be those containing negative charges (Asp > Glu) or aromatic residues in positions 1', 2', or 3' (delta delta GT++ values of 2-5 kJ); the negative charge provided by the C-terminus of the substrate also appears to be important, since the amide and O-Me ester derivatives caused a change in delta delta GT++ values of -7 to -8 kJ from the reference peptide. The stimulating effect of the negative charges is consistent with the inhibitory effect of positive charges in similar peptides (Krishna RG, Wold F, 1992, Protein Sci 1:582-589), and the proposed active site model incorporates subsites for both charge-charge and hydrophobic interactions. In assessing all the data, it is clear that the properties of the individual substrates reflect the total make-up of each peptide and not only the effect of a single residue in a given position.(ABSTRACT TRUNCATED AT 250 WORDS)
为了持续探索可能影响蛋白质 - 蛋白质(肽)相互作用的特异性决定因素的类型,已对许多短(2 - 5个残基)的乙酰化肽作为乙酰氨基酰肽水解酶(EC 3.4.19.1)的底物进行了比较。参考底物是Ac - AAAA,大多数其他底物是通过单个氨基酸取代从这个基本结构衍生而来的。通过标准稳态动力学测定不同底物的Km和kcat,并使用从kcat / Km得出的相应ΔΔGT ++值进行比较,将Ac - AAAA的ΔΔGT ++设为0。发现最佳底物是在1'、2'或3'位含有负电荷(Asp > Glu)或芳香族残基的那些(ΔΔGT ++值为2 - 5 kJ);底物C末端提供的负电荷似乎也很重要,因为酰胺和O - 甲基酯衍生物使参考肽的ΔΔGT ++值变化了 - 7至 - 8 kJ。负电荷的刺激作用与类似肽中正电荷的抑制作用一致(Krishna RG,Wold F,1992,Protein Sci 1:582 - 589),并且所提出的活性位点模型包含了用于电荷 - 电荷和疏水相互作用的亚位点。在评估所有数据时,很明显各个底物的性质反映了每个肽的整体组成,而不仅仅是给定位置单个残基的作用。(摘要截断于250字)