Plant Proteomics 2008
DOI: 10.1002/9780470369630.ch36
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Tap‐Tagging System in Rice for Protein Complex Isolation

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Cited by 3 publications
(2 citation statements)
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“…Among the seven proteins that were identified by MS, dynamin interaction with OsGI was verified with co-immunoprecipitation using a myc-tagged OsGI. This study furthers the use of previously established TAP methodology [43,44] in isolating novel interacting proteins with overexpressed target proteins of interest.…”
Section: Osgi-interactionsupporting
confidence: 63%
“…Among the seven proteins that were identified by MS, dynamin interaction with OsGI was verified with co-immunoprecipitation using a myc-tagged OsGI. This study furthers the use of previously established TAP methodology [43,44] in isolating novel interacting proteins with overexpressed target proteins of interest.…”
Section: Osgi-interactionsupporting
confidence: 63%
“…14‐3‐3 and its client proteins are well studied in plants using the combination of affinity chromatography and proteomics approaches (see review, 59). Tandem affinity purification (TAP)‐tagging system is well established in rice 60 and Arabidopsis 61 to isolate protein complex. In this TAP‐tagging system, isolated protein complex is digested with proteolytic enzyme(s), typically trypsin, and analyzed by MS. Alternatively, protein complex is separated by 1‐DE and excised protein bands are trypsin digested followed by analysis with MS to identify interacting proteins.…”
Section: Technique Of Choice: Classical Protein Extraction and Sepamentioning
confidence: 99%