Lowenson Jonathan D, Shmanai Vadim V, Shklyaruck Denis, Clarke Steven G, Shchepinov Mikhail S
Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California, Los Angeles, CA, 90095-1569, USA.
Institute of Physical Organic Chemistry, National Academy of Science of Belarus, Minsk, 220072, Belarus.
Amino Acids. 2016 Sep;48(9):2189-96. doi: 10.1007/s00726-016-2250-z. Epub 2016 May 12.
Racemization in proteins and peptides at sites of L-asparaginyl and L-aspartyl residues contributes to their spontaneous degradation, especially in the biological aging process. Amino acid racemization involves deprotonation of the alpha carbon and replacement of the proton in the opposite stereoconfiguration; this reaction is much faster for aspartate/asparagine than for other amino acids because these residues form a succinimide ring in which resonance stabilizes the carbanion resulting from proton loss. To determine if the replacement of the hydrogen atom on the alpha carbon with a deuterium atom might decrease the rate of racemization and thus stabilize polypeptides, we synthesized a hexapeptide, VYPNGA, in which the three carbon-bound protons in the asparaginyl residue were replaced with deuterium atoms. Upon incubation of this peptide in pH 7.4 buffer at 37 °C, we found that the rate of deamidation via the succinimide intermediate was unchanged by the presence of the deuterium atoms. However, the accumulation of the D-aspartyl and D-isoaspartyl-forms resulting from racemization and hydrolysis of the succinimide was decreased more than five-fold in the deuterated peptide over a 20 day incubation at physiological temperature and pH. Additionally, we found that the succinimide intermediate arising from the degradation of the deuterated asparaginyl peptide was slightly less likely to open to the isoaspartyl configuration than was the protonated succinimide. These findings suggest that the kinetic isotope effect resulting from the presence of deuteriums in asparagine residues can limit the accumulation of at least some of the degradation products that arise as peptides and proteins age.
蛋白质和肽中L-天冬酰胺基和L-天冬氨酰残基位点的消旋化会导致其自发降解,尤其是在生物衰老过程中。氨基酸消旋化涉及α-碳原子的去质子化以及相反立体构型中质子的取代;天冬氨酸/天冬酰胺的这种反应比其他氨基酸快得多,因为这些残基形成了一个琥珀酰亚胺环,共振使质子损失产生的碳负离子稳定。为了确定用氘原子取代α-碳原子上的氢原子是否可能降低消旋化速率从而稳定多肽,我们合成了一种六肽VYPNGA,其中天冬酰胺基残基中与碳相连的三个质子被氘原子取代。在37°C的pH 7.4缓冲液中孵育该肽时,我们发现通过琥珀酰亚胺中间体的脱酰胺化速率不受氘原子存在的影响。然而,在生理温度和pH下孵育20天的过程中,氘代肽中由琥珀酰亚胺的消旋化和水解产生的D-天冬氨酰和D-异天冬氨酰形式的积累减少了五倍以上。此外,我们发现氘代天冬酰胺肽降解产生的琥珀酰亚胺中间体比质子化琥珀酰亚胺更不容易向异天冬氨酰构型开放。这些发现表明,天冬酰胺残基中氘的存在所产生的动力学同位素效应可以限制随着肽和蛋白质老化而产生的至少一些降解产物的积累。