use of cdna tiling arrays for identifying protein interactions selected by in vitro display technologies利用cdna花砖阵列识别蛋白质交互选择体外显示技术.pdfVIP

use of cdna tiling arrays for identifying protein interactions selected by in vitro display technologies利用cdna花砖阵列识别蛋白质交互选择体外显示技术.pdf

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
use of cdna tiling arrays for identifying protein interactions selected by in vitro display technologies利用cdna花砖阵列识别蛋白质交互选择体外显示技术

Use of cDNA Tiling Arrays for Identifying Protein Interactions Selected by In Vitro Display Technologies Kenichi Horisawa, Nobuhide Doi, Hiroshi Yanagawa* Department of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Japan Abstract In vitro display technologies such as mRNA display are powerful screening tools for protein interaction analysis, but the final cloning and sequencing processes represent a bottleneck, resulting in many false negatives. Here we describe an application of tiling array technology to identify specifically binding proteins selected with the in vitro virus (IVV) mRNA display technology. We constructed transcription-factor tiling (TFT) arrays containing ,1,600 open reading frame sequences of known and predicted mouse transcription-regulatory factors (334,372 oligonucleotides, 50-mer in length) to analyze cDNA fragments from mRNA-display screening for Jun-associated proteins. The use of the TFT arrays greatly increased the coverage of known Jun-interactors to 28% (from 14% with the cloning and sequencing approach), without reducing the accuracy (,75%). This method could detect even targets with extremely low expression levels (less than a single mRNA copy per cell in whole brain tissue). This highly sensitive and reliable method should be useful for high-throughput protein interaction analysis on a genome-wide scale. Citation: Horisawa K, Doi N, Yanagawa H (2008) Use of cDNA Tiling Arrays for Identifying Protein Interactions Selected by In Vitro Display Technologies. PLoS ONE 3(2): e1646. doi:10.1371/journal.pone.0001646 ´ ´ Editor: Stephen W. Michnick, Universite de Montreal, Canada Received October 21, 2007; Accepted January 28, 2008; Published February 20, 2008 Copyright: 2008 Horisawa et al. This

您可能关注的文档

文档评论(0)

118zhuanqian + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档