Department of Chemistry, The Scripps Research Institute, Scripps Florida, 120 Scripps Way, Jupiter, Florida 33458, USA.
J Am Chem Soc. 2012 Oct 17;134(41):17015-8. doi: 10.1021/ja308871v. Epub 2012 Oct 3.
Protein arginine deiminases (PADs) catalyze the hydrolysis of peptidyl arginine to form peptidyl citrulline. Abnormally high PAD activity is observed in a host of human diseases, but the exact role of protein citrullination in these diseases and the identities of specific citrullinated disease biomarkers remain unknown, largely because of the lack of readily available chemical probes to detect protein citrullination. For this reason, we developed a citrulline-specific chemical probe, rhodamine-phenylglyoxal (Rh-PG), which we show can be used to investigate protein citrullination. This methodology is superior to existing techniques because it possesses higher throughput and excellent sensitivity. Additionally, we demonstrate that this probe can be used to determine the kinetic parameters for a number of protein substrates, monitor drug efficacy, and identify disease biomarkers in an animal model of ulcerative colitis that displays aberrantly increased PAD activity.
精氨酸蛋白脱亚氨酶(PADs)催化肽基精氨酸水解生成肽基瓜氨酸。在许多人类疾病中观察到异常高的 PAD 活性,但蛋白质瓜氨酸化在这些疾病中的确切作用以及特定的瓜氨酸化疾病生物标志物的身份仍然未知,这主要是因为缺乏易于获得的化学探针来检测蛋白质瓜氨酸化。出于这个原因,我们开发了一种瓜氨酸特异性化学探针,即罗丹明-苯乙醛(Rh-PG),我们证明它可用于研究蛋白质瓜氨酸化。这种方法优于现有技术,因为它具有更高的通量和出色的灵敏度。此外,我们证明该探针可用于确定许多蛋白质底物的动力学参数,监测药物疗效,并在显示异常增加 PAD 活性的溃疡性结肠炎动物模型中鉴定疾病生物标志物。