Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601, Japan.
Free Radic Biol Med. 2011 Jul 1;51(1):1-4. doi: 10.1016/j.freeradbiomed.2011.02.037. Epub 2011 Mar 30.
We developed a procedure to measure 4-hydroxy-2-nonenal (HNE)-amino acid adducts using the fluorescent probe 2-aminopyridine (2-AP). The method is based on the fact that HNE forms Michael addition-type amino acid adducts possessing an aldehyde functionality, which upon reaction with 2-AP in the presence of NaBH₃CN can be converted to their pyridylaminated derivatives. The HNE-amino acid adducts, namely Michael addition-type HNE-cysteine, HNE-histidine, and HNE-lysine adducts, after pyridylamination were resistant to conventional acid-hydrolysis conditions for protein (6N HCl/110°C/24 h) and could be detected by HPLC with a fluorescence detector. The reductive amination-based fluorescent labeling of HNE adducts is a simple and accurate technique that may be widely used to reveal increased levels of covalently modified proteins with HNE and its related aldehydes during aging and disease.
我们开发了一种使用荧光探针 2-氨基吡啶(2-AP)测量 4-羟基-2-壬烯醛(HNE)-氨基酸加合物的方法。该方法基于 HNE 形成具有醛基的迈克尔加成型氨基酸加合物的事实,所述醛基在 NaBH₃CN 的存在下与 2-AP 反应,可以转化为其吡啶基氨基化衍生物。HNE-氨基酸加合物,即迈克尔加成型 HNE-半胱氨酸、HNE-组氨酸和 HNE-赖氨酸加合物,经吡啶基氨基化后,可耐受蛋白质的常规酸水解条件(6N HCl/110°C/24 h),并可通过 HPLC 用荧光检测器检测到。基于还原胺化的 HNE 加合物的荧光标记是一种简单而准确的技术,可广泛用于揭示衰老和疾病过程中与 HNE 及其相关醛结合的共价修饰蛋白水平的增加。