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Applying Protein-Peptide Interactions to Fluorescently Label Proteins in S. Cerevisiae

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개인저자Hinrichsen, Michael.
단체저자명Yale University.
서명/저자사항Applying Protein-Peptide Interactions to Fluorescently Label Proteins in S. Cerevisiae.
발행사항[S.l.] : Yale University., 2018
발행사항Ann Arbor : ProQuest Dissertations & Theses, 2018
형태사항121 p.
소장본 주기School code: 0265.
ISBN9780438193673
일반주기 Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
Adviser: Lynne Regan.
요약Cells are highly complex, organized and dynamic machines, driven by intricate protein-based machinery. Understanding how this protein machinery produces the cellular processes we observe requires more than simply characterizing the individual pa
요약While a number of methods can be used to fluorescently label a protein of interest, there is no one method that is suitable for all imaging applications. Oftentimes, picking the appropriate labeling method requires balancing a variety of competi
요약SpyCatcher/SpyTag are a protein/peptide pair that bind one another and form an irreversible isopeptide bond in solution. I harnessed this interaction pair to fluorescently label proteins in vivo by fusing SpyTag (13 amino acids) to the protein o
요약Additionally. I have also investigated the use of a reversible protein/peptide interaction to fluorescently label proteins in S. cerevisiae. TRAPs are artificial binding domains developed in the Regan lab that bind 5 amino acid long, C-terminal
요약Thus, I have shown that a variety of protein/peptide interactions can be used to fluorescently label proteins in vivo and have developed the tools and protocols necessary to fluorescently label proteins of interest in yeast. Our SpyCatcher/SpyTa
일반주제명Biochemistry.
Biophysics.
Cellular biology.
언어영어
기본자료 저록Dissertation Abstracts International79-11B(E).
Dissertation Abstract International
대출바로가기http://www.riss.kr/pdu/ddodLink.do?id=T15000822

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