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Purification and Characterization of PCR-Inhibitory Components in Blood Cells
Open accessAbstract
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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Cites
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Lactoferrin: molecular structure and biological function
Lönnerdal, B., & Iyer, S. (1995) · Annual Review of Nutrition · doi:10.1146/annurev.nu.15.070195.000521 · Cited by 781
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Schrader, C., Schielke, A., Ellerbroek, L., & Johne, R. (2012) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2012.05384.x · Cited by 2,118
Poon, L. L., Wong, B. W., Ma, E. H., Chan, K. H., Chow, L. M., Abeyewickreme, W., Tangpukdee, N., Yuen, K. Y., Guan, Y., Looareesuwan, S., et al. (2006) · Clinical Chemistry · doi:10.1373/clinchem.2005.057901 · Cited by 476
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Moldovan, L., Batte, K. E., Trgovcich, J., Wisler, J., Marsh, C. B., & Piper, M. (2014) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12236 · Cited by 436
Tzanakaki, G., Tsopanomichalou, M., Kesanopoulos, K., Matzourani, R., Sioumala, M., Tabaki, A., & Kremastinou, J. (2005) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2005.01109.x · Cited by 106
Metadata
- Authors
- Al-Soud, W. A., & Rådström, P.
- Venue
- Journal of Clinical Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2001-02
- Volume
- 39
- Issue
- 2
- Pages
- 485-493
- ISSN
- 0095-1137 (ISSN-L)
- 1098-660X
- OpenAlex
- W2095989309
- Cited by
- 944
- References
- 2
- FWCI
- 7.06
- Type
- journal article
- Language
- en
- Open access
- green
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