Bhatwadekar A D, Ghole V S
Molecular Biology Laboratory, Division of Biochemistry, Department of Chemistry, University of Pune, Pune, India.
J Clin Lab Anal. 2005;19(1):11-5. doi: 10.1002/jcla.20048.
Estimation of advanced glycation end products (AGEs) by determining fluorescence is based on the use of a standard calibrator prepared by incubating bovine serum albumin (BSA) and glucose at 37 degrees C for 60 days. In the present study we attempted to reduce the duration of incubation to 4 days by increasing the temperature to 50 degrees C. It is noteworthy that incubation at 50 degrees C resulted in the rapid production of an AGE-BSA standard calibrator within 4 days. Aminoguanidine reduced the intensity of the glycation-induced fluorescence, while the addition of lysine intensified the reaction, as shown by the calibrator incubated at 37 degrees C. The protein carbonyl content was shown to increase in the rapidly-formed standard calibrator. Thus we conclude that a simple increase in temperature and the addition of lysine (0.1M) can accelerate the process of glycation-induced fluorescence. This calibrator can be used effectively in fluorescence assays of AGEs.
通过测定荧光来估算晚期糖基化终产物(AGEs),其依据是使用一种标准校准物,该校准物通过在37℃下将牛血清白蛋白(BSA)与葡萄糖孵育60天制备而成。在本研究中,我们试图通过将温度提高到50℃,将孵育时间缩短至4天。值得注意的是,在50℃下孵育导致在4天内快速产生了AGE-BSA标准校准物。氨基胍降低了糖基化诱导的荧光强度,而添加赖氨酸增强了反应,如在37℃下孵育的校准物所示。结果表明,在快速形成的标准校准物中蛋白质羰基含量增加。因此我们得出结论,简单地提高温度并添加赖氨酸(0.1M)可以加速糖基化诱导荧光的过程。这种校准物可有效地用于AGEs的荧光测定。