Bilirubin-protein interactions monitored by difference spectroscopy.

نویسندگان

  • K O Ash
  • M Holmer
  • C S Johnson
چکیده

Difference spectroscopy is used to monitor bilirubin-protein interactions, to assess the residual binding capacity of proteins for bilirubin. A change in the difference spectra monitored at 482 nm is directly proportional to bound bilirubin up to a molar ratio of bilirubin to albumin of approximately 1; increasing bilirubin beyond the 1:1 molar ratio does not further change the difference spectra. After excess free bilirubin is added, the change in the difference spectrum is proportional to the residual binding capacity of the serum for bilirubin. The risk of kernicterus among neonates may be assessed by monitoring the residual bilirubin binding capacity of serum. This report summarizes our research effort leading to an assay method which requires only 40 microliter of serum and can be completed in less than 10 min.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The effect of hepatic protection of hydro alcoholic extract of Thyme in rats (Thymus daenensis).

Background  Thyme has high antioxidant properties due to polyphenols and flavonoids. The aim of this study was to evaluate the effects of hepatic protection of Thyme on the toxicity induced by carbon tetrachloride in rats. Materials and methods In this experimental study, 40 male Wistar rats weighing 220-250 grams were randomly divided into five groups of eight. One group was monitored and f...

متن کامل

Label-free screening of drug-protein interactions by time-resolved Fourier transform infrared spectroscopic assays exemplified by Ras interactions.

Time-resolved Fourier transform infrared (FT-IR) spectroscopy can reveal molecular details of protein interactions. Analysis of difference spectra selects the absorptions of respective protein groups involved in an interaction against the background of the whole sample. By comparison of the same difference spectrum with and without a small molecule, one can determine whether the small molecule ...

متن کامل

Bilirubin binding to myelin basic protein, histones and its inhibition in vitro of cerebellar protein synthesis.

The binding of unconjugated bilirubin to bovine CNS myelin basic protein and to lysine and arginine rich histones has been demonstrated by means of difference spectroscopy and circular dichroism spectroscopy. This is the first demonstration of a brain specific protein that can bind bilirubin and provides a mechanism for bilirubin retention in brain as well as a mechanism for interfering with th...

متن کامل

FOLDING OF THE INTERACTION OF HISTONE HI WITH SODIUM N-DODECYL SULPHATE

The effects of sodium n-dodecyl sulphate (SDS) on the structure of histone HI has been studied by a combination of e:quilibrium dialysis, U.V. spectroscopy ; polyacrylamide gel electrophoresis, protein titration and viscometery techniques using, 2.5 mM phosphate buffer, pH 6.4. The interaction of H, and SDS in contrast tomanyothel-protein-SDS interactions is organized between V 40 to 70. A...

متن کامل

آیا بیلی روبین می‌تواند شاخصی برای پیشگویی بیماری شریان کرونر باشد؟

Background and Aim: Oxidative interactions such as the formation of oxygen, peroxy radicals and LDL-cholesterol oxidation are involved in the development of atherosclerosis process This study aims to examine the relationship between serum bilirubin levels and the incidence of coronary artery disease. Materials and Methods: Eighty-five patients and ninety-two healthy volunteers were enrolled i...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Clinical chemistry

دوره 24 9  شماره 

صفحات  -

تاریخ انتشار 1978