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dc.contributor.authorAnson, Jonathan R.
dc.contributor.authorLu, Chia-Hung
dc.contributor.authorCui, Lingwen
dc.contributor.authorYang, Xiaojing
dc.contributor.authorXu, Shaohua
dc.date.accessioned2013-06-25T12:16:55Z
dc.date.available2013-06-25T12:16:55Z
dc.date.issued2013-01
dc.identifier.citationAnson, J., Lu, C., Cui, L., Yang, X., Xu, S., "Techniques to quantify the size of protein colloids in amyloid fiber formation," Open Journal of Biophysics, Vol. 3 No. 1, 2013, pp. 22-32. doi: 10.4236/ojbiphy.2013.31003.en_US
dc.identifier.urihttp://hdl.handle.net/11141/59
dc.description.abstractA new method for the analysis of protein colloidal diameter has been developed using three existing protein concentration quantification techniques, absorption at 280 nm, colloidal gold assay, and DC protein assay. Protein colloids are formed in the process of aggregation and are thought to be intermediates in protein self-assembly and formation of amyloid fiber. Deposition of the protein fibers in tissues leads to numerous human diseases including Alzheimer’s. Lysozyme was incubated at pH 2.0, 55°C, an environment conducive to amyloid fiber formation. The protein colloids present in the supernatant of the samples after centrifugation were studied over a time course of 30 days. The OD 280 assay detects total protein concentration based on absorption of radiation in the near UV. The colloidal gold assay and DC protein assay only measure colloidal sphere surface protein concentration. Due to the surface plasmon resonance, the light absorption spectrum changes when proteins bind to colloidal gold particles. Using the measured protein concentration on the surface of protein colloids along with the total measured protein concentration in the entire protein colloidal spheres, an interior protein concentration for all colloids is obtained. The protein colloidal sphere size can be calculated by using the ratio between the interior protein concentration and total protein concentration. Results indicate that the colloidal gold assay, DC protein assay, and OD 280 assay can be used to quantify the size of the protein colloids. The colloidal gold assay and DC protein assay are both independently effective in analysis of surface protein concentration in protein colloids. The DC protein assay was found to be much quicker in data production as it only requires 15 minutes of incubation time. The DC protein assay was also more reliable than the colloidal gold assay in accuracy and precision of results.en_US
dc.language.isoen_USen_US
dc.rightsThis published article is available in accordance with the publisher's policy. It may be subject to U.S. copyright law.en_US
dc.rights.urihttp://www.scirp.org/aboutUs/en_US
dc.titleTechniques to quantify the size of protein colloids in amyloid fiber formationen_US
dc.typeArticleen_US
dc.identifier.doi10.4236/ojbiphy.2013.31003


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