A functional quantitative polymerase chain reaction assay for ricin, Shiga toxin, and related ribosome-inactivating proteins

作者：Melchior William B Jr^*; Tolleson William H

来源：Analytical Biochemistry, 2010, 396(2): 204-211.

DOI：10.1016/j.ab.2009.09.024

• Ricin
• Ribosome-inactivating proteins
• Quantitative PCR
• Reverse transcriptase

The potent toxins ricin, abrin, and other ribosome-inactivating proteins deadenylate a specific base in 28S ribosomal RNA that destroys ribosomes and leads to cell death. We have taken advantage of the fact that reverse transcriptase preferentially inserts an adenine opposite to an abasic site in RNA to create a quantitative polymerase chain reaction (PCR) assay to detect the damage. This assay detects as little as 30 pg of ricin. We used the assay to study enzymatic properties of ricin such as pH and temperature optima (pH 4.5-5.0 and 60 degrees C). Published by Elsevier Inc.

• 出版日期2010-1-15