Purification and Characterization of PCR-Inhibitory Components in Blood Cells

分子生物学 血红蛋白 乳铁蛋白 底漆(化妆品) 生物 DNA 色谱法 生物化学 化学 有机化学
作者
Waleed Abu Al‐Soud,Peter Rådström
出处
期刊:Journal of Clinical Microbiology [American Society for Microbiology]
卷期号:39 (2): 485-493 被引量:927
标识
DOI:10.1128/jcm.39.2.485-493.2001
摘要

ABSTRACT In a recent study, immunoglobulin G in human plasma was identified as a major inhibitor of diagnostic PCR (W. Abu Al-Soud, L. J. Jönsson, and P. Rådström. J. Clin. Microbiol. 38:345–350, 2000). In this study, two major PCR inhibitors in human blood cells were purified using size exclusion and anion-exchange chromatographic procedures. Based on N-terminal amino acid sequencing and electrophoretic analysis of the purified polypeptides, hemoglobin and lactoferrin were identified as PCR-inhibitor components in erythrocytes and leukocytes, respectively. When different concentrations of hemoglobin or lactoferrin were added to PCR mixtures of 25 μl containing 10 different thermostable DNA polymerases and 1 ng of Listeria monocytogenes DNA as template DNA, Ampli Taq Gold, Pwo , and Ultma were inhibited in the presence of ≤1.3 μg of hemoglobin and ≤25 ng of lactoferrin, while rTth and Tli were found to resist inhibition of at least 100 μg of hemoglobin. In addition, the quantitative effects of seven low-molecular-mass inhibitors, present in blood samples or degradation products of hemoglobin, on real-time DNA synthesis of rTth using the LightCycler Instrument were investigated. A reaction system based on a single-stranded poly(dA) template with an oligo(dT) primer annealed to the 3′ end was used. It was found that the addition of 0.25 to 0.1 mg of bile per ml, 2.5 mM CaCl 2 , 0.25 mM EDTA, 5 μM FeCl 3 , and 0.01 IU of heparin per ml reduced the fluorescence to approximately 76, 70, 46, 17, and 51%, respectively. Finally, the effects of nine amplification facilitators were studied in the presence of hemoglobin and lactoferrin. Bovine serum albumin (BSA) was the most efficient amplification facilitator, so that the addition of 0.4% (wt/vol) BSA allowed Ampli Taq Gold to amplify DNA in the presence of 20 instead of 1 μg of hemoglobin and 500 instead of 5 ng of lactoferrin. Including 0.02% (wt/vol) gp32, a single-stranded-DNA binding protein, in the reaction mixture of Ampli Taq Gold was also found to reduce the inhibitory effects of hemoglobin and lactoferrin.

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