Abstract

BackgroundC-reactive protein (CRP) is a marker of inflammation and a risk predictor of cardiovascular disease. Current CRP assays are focused on the quantification of the CRP levels as pentamers. However, CRP can be present as other multimeric forms. There will be a market need to measure the CRP multimeric structure in addition to the levels in human populations. To meet this need, we investigated whether the long-term archived samples could be used instead of freshly collected samples.Methodology/Principal FindingsThe specimens of serum, plasma and tissues were collected from transgenic rats expressing the human CRP. These samples were stored at 4°C, −20°C and −80°C for different periods. Non-denaturing Western blot analysis was used to observe the influence of storage conditions to multimeric structures of human CRP. Our results showed that there was no difference on multimeric structures of human CRP between samples stored at 4°C, −20°C and −80°C, between samples stored at −80°C for twenty-four hours and three months, and between plasma and serum.Conclusions/SignificanceThis study implicated that archived samples stored at these conditions in those large longitudinal studies could be used for investigating the multimeric structures of CRP. Our report may speed up these researches and save labors and budget by enabling them to use currently available archived samples rather than freshly collected samples.

Highlights

  • C-reactive protein (CRP) is a member of the pentraxin protein family

  • This study assessed the stability of multimeric structure of human C-reactive protein in archived specimens of blood and Influence of storage temperature on the CRP multimeric structure The serum samples that were stored at different temperature for three months were analyzed by Western Blot

  • In young rats (7 weeks old and 18 weeks old), human CRP was present in serum as both pentamers and dimers

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Summary

Introduction

C-reactive protein (CRP) is a member of the pentraxin protein family. CRP is an ancient and ubiquitous protein in vertebrates and invertebrates. Serum CRP levels are helpful in the prediction of prognosis and coronary involvement of the patients with Kawasaki disease, when considering age [19,20]. Synergistic influence of CRP levels and the at risk genotype of the CFH gene resulted in a super-additive risk for prevalent late AMD and AMD progression [22]. These studies have demonstrated the value of CRP in the pre-symptom risk predictions of human diseases. There will be a market need to measure the CRP multimeric structure in addition to the levels in human populations To meet this need, we investigated whether the long-term archived samples could be used instead of freshly collected samples

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