Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, Indiana 47907-2084, USA.
J Am Chem Soc. 2012 Jul 18;134(28):11412-4. doi: 10.1021/ja304778j. Epub 2012 Jul 6.
Gas-phase conjugation to unprotonated arginine side-chains via N-hydroxysuccinimide (NHS) esters is demonstrated through both charge reduction and charge inversion ion/ion reactions. The unprotonated guanidino group of arginine can serve as a strong nucleophile, resulting in the facile displacement of NHS from NHS esters with concomitant covalent modification of the arginine residue. This reactivity is analogous to that observed with unprotonated primary amines such as the N-terminus or ε-amino group of lysine. In solution, however, the arginine residues tend to be protonated at pH values low enough to prevent hydrolysis of NHS esters, which would render them relatively unreactive with NHS esters. This work demonstrates novel means for gas-phase conjugation to arginine side chains in polypeptide ions.
通过电荷还原和电荷反转的离子/离子反应,展示了通过 N-羟基琥珀酰亚胺 (NHS) 酯在气相中与未质子化的精氨酸侧链连接。精氨酸的未质子化胍基可以作为一个强亲核试剂,导致 NHS 从 NHS 酯中容易取代,同时精氨酸残基发生共价修饰。这种反应性类似于与未质子化的伯胺(如赖氨酸的 N-末端或ε-氨基)观察到的反应性相似。然而,在溶液中,由于 pH 值足够低,精氨酸残基往往被质子化,以防止 NHS 酯的水解,这使得它们与 NHS 酯相对不反应。这项工作展示了在多肽离子中与精氨酸侧链进行气相连接的新方法。