Download Abstract The development of a RNA-aptamer

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Bimolecular fluorescence complementation wikipedia , lookup

Surround optical-fiber immunoassay wikipedia , lookup

Cooperative binding wikipedia , lookup

Nuclear magnetic resonance spectroscopy of proteins wikipedia , lookup

Protein purification wikipedia , lookup

Protein–protein interaction wikipedia , lookup

RNA-binding protein wikipedia , lookup

Western blot wikipedia , lookup

Transcript
Abstract The development of a RNA-aptamer-based optical biosensor
(aptasensor) for C-reactive protein (CRP) is reported.
CRP is an important clinical biomarker; it was the first acutephase protein to be
discovered (1930) and is a sensitive sistemi marker of inflammation and tissue
damage. It has also a prognostic value for patients with acute coronary
syndrome. The average concentration of CRP in serum is 0.8 ppm and it
increases in response to a variety of inflammatory stimuli, such as trauma, tissue
necrosis, infection and myocardial infarction. The interaction between the 44base RNA aptamer and the target analyte CRP is studied. In particular, the
influence of the aptamer immobilization procedure (chemistry, length,
concentration), as well as the binding conditions, i.e., the influence on the
binding of different buffers, the presence of Ca2+ ion and the specificity (against
human serum albumin) have been evaluated. Using the best working conditions,
we achieved a detection limit of 0.005 ppm, with good selectivity towards
human serum albumin. Some preliminary
experiments in serum are reported.