Department of Chemistry, Binghamton University, Binghamton, New York 13902, United States.
Bioconjug Chem. 2011 Oct 19;22(10):1954-61. doi: 10.1021/bc2001566. Epub 2011 Oct 4.
Hydrazone formation and similar reactions are highly versatile and specific, but their application to biological systems has been limited by their characteristically slow reaction kinetics at neutral pH. Catalysis of these reactions through imine formation with aromatic amines such as aniline has broadened the applicability of these reactions to biomolecular labeling. High concentrations of the catalyst are necessary, which may be incompatible with the native structure of certain proteins. In this study, we investigated the utility of 4-aminophenylalanine (4a-Phe) as a catalyst for these reactions. We find that 4a-Phe is nearly as effective as aniline in catalyzing hydrazone formation between the reactive amino acid 3-formyltyrosine (3f-Tyr) and hydrazine-containing fluorophores, both free in solution and incorporated into the protein tubulin. The catalyst 4a-Phe maintains ∼70% of the catalytic efficacy of aniline and is less detrimental to the native structure of tubulin. Examination of the temperature dependence of imine formation between 3f-Tyr and 4a-Phe shows an increase in imine concentration accompanying a decrease in temperature, confirming the exothermic nature of the equilibrium reaction. Interestingly, decreasing the temperature of the 4a-Phe-catalyzed hydrazone reaction between 3f-Tyr and the fluorophore 7-hydrazinyl-4-methylcoumarin increases the overall rate of the reaction. This result indicates that the temperature dependence of the catalyst-aldehyde equilibrium is greater than the temperature dependence of the rate constant for hydrazone formation from this intermediate, and that the rate of hydrazone formation a direct function of the concentration of the intermediate imine. These results provide a platform for conducting nucleophilic catalysis under conditions that are more compatible with biomolecular targets than previously demonstrated, thereby expanding the utility of hydrazone ligations in biological systems.
腙的形成和类似反应具有高度的多功能性和特异性,但由于在中性 pH 下反应动力学较慢,其在生物系统中的应用受到限制。通过与芳香胺(如苯胺)形成亚胺来催化这些反应,拓宽了这些反应在生物分子标记中的应用。需要高浓度的催化剂,但这可能与某些蛋白质的天然结构不兼容。在这项研究中,我们研究了 4-氨基苯丙氨酸(4a-Phe)作为这些反应催化剂的实用性。我们发现,4a-Phe 在催化 3-甲酰基酪氨酸(3f-Tyr)与含肼荧光团之间形成腙的反应中,与苯胺一样有效,无论是在溶液中游离的还是整合到蛋白质微管蛋白中的。催化剂 4a-Phe 保持了苯胺催化效能的约 70%,对微管蛋白的天然结构的损害较小。考察 3f-Tyr 和 4a-Phe 之间亚胺形成的温度依赖性表明,随着温度的降低,亚胺浓度增加,证实了平衡反应的放热性质。有趣的是,降低 3f-Tyr 和荧光团 7-肼基-4-甲基香豆素之间的 4a-Phe 催化腙反应的温度会增加反应的总速率。这一结果表明,催化剂-醛平衡的温度依赖性大于该中间体形成腙的速率常数的温度依赖性,并且腙的形成速率是中间亚胺浓度的直接函数。这些结果为在比以前更能与生物分子靶标兼容的条件下进行亲核催化提供了一个平台,从而扩展了腙键合在生物系统中的应用。