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請使用永久網址來引用或連結此文件:
http://ir.cmu.edu.tw/ir/handle/310903500/29132
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題名: | Characterization of spiculation on ultrasound lesions |
作者: | Huang, SF;Chang, RF;Chen, DR;Moon, WK |
貢獻者: | 附設醫院外科部;Natl Chung Cheng Univ, Dept Comp Sci & Informat Engn, Chiayi 621, Taiwan;China Med Coll & Hosp, Dept Gen Surg, Taichung 404, Taiwan;Seoul Natl Univ Hosp, Dept Diagnost Radiol, Coll Med, Seoul 110744, South Korea |
日期: | 2004 |
上傳時間: | 2010-09-24 14:23:13 (UTC+8) |
出版者: | IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC |
摘要: | Severe acute respiratory syndrome (SARS) is an emerging infectious disease associated with a novel coronavirus and causing worldwide outbreaks. SARS coronavirus (SARS-CoV) is an enveloped RNA virus, which contains several structural proteins. Among these proteins, spike (S) protein is responsible for binding to specific cellular receptors and is a major antigenic determinant, which induces neutralizing antibody. In order to analyze the antigenicity and receptor-binding ability of SARS-CoV S protein, we expressed the S protein in Escherichia coli using a pET expression vector. After the isopropyl-p-D-thiogalactoside induction, S protein was expressed in the soluble form and purified by nickel-affinity chromatography to homogeneity. The amount of S protein recovered was 0.2-0.3 mg/100 ml bacterial culture. The S protein was recognized by sera from SARS patients by ELISA and Western blot, which indicated that recombinant S protein retained its antigenicity. By biotinylated ELISA and Western blot using biotin-labeled S protein as the probe, we identified 130-kDa and 140-kDa proteins in Vero cells that might be the cellular receptors responsible for SARS-CoV infection. Taken together, these results suggested that recombinant S protein exhibited the antigenicity and receptor-binding ability, and it could be a good candidate for further developing SARS vaccine and anti-SARS therapy. (C) 2003 Elsevier Inc. All rights reserved. |
關聯: | IEEE TRANSACTIONS ON MEDICAL IMAGING 23(1):111-121 |
顯示於類別: | [台中附設醫院] 期刊論文
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