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Identification of CED-3 substrates by a yeast-based screening method.

作者信息

Kim Sung Yun, Valencia Marcela, Lee Eui Seung, Park Daeho, Oh Myungsok, Xue Ding, Park Woo Jin

机构信息

Department of Life Science, National Research Laboratory of Proteolysis, Kwangju Institute of Science and Technology (K-JIST), 1 Oryong-dong, Puk-gu, Kwangju, 500-712, Korea.

出版信息

Mol Biotechnol. 2004 May;27(1):1-6. doi: 10.1385/MB:27:1:01.

Abstract

Identifying cellular substrates repertoire of individual proteases will facilitate our understanding of their physiological and pathological roles. In this article, we employed a yeast-based screening method to isolate CED-3 substrates. This method uses a transcription factor anchored to the plasma membrane by fusion to a library of cellular protein sequences. When a fusion protein is cleaved by CED-3, the transcription factor is released from the plasma membrane and enters the nucleus where it turns on the expression of reporter genes. We identified seven candidate clones by screening a genomic library using this method. Of these seven clones, two were cleaved by purified CED-3 in vitro. Therefore, the method described here may be generally used for genomewide screening to isolate potential substrates of specific proteases.

摘要

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