FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2044594717> ?p ?o ?g. }

• W2044594717 endingPage "140" @default.
• W2044594717 startingPage "131" @default.
• W2044594717 abstract "Abstract The importance of high‐throughput analyses of protein abundances and functions is interestingly increasing in genomic/proteomic studies. In such postgenome sequencing era, a protein‐detecting chip, in which a large number of molecules specifically capturing target proteins (capturing agents) such as antibodies, recombinant proteins, and small molecules are arrayed onto solid, wet, or semi‐wet substrates, enables comprehensive analysis of proteomes by a single experiment. However, whole proteomes are generally complicated for comprehensive analyses so that alternative approaches to subproteome analysis categorized by protein functions and binding properties (focused proteome) would be effective. Approaching the goal of development of designed peptide chip for protein analysis, diversity increases in peptide structures and validation of target proteins are needed. We herein describe design and synthesis of nucleobase amino acid (NBA)‐containing peptides, selection of nucleic acid‐related proteins derived from S. cerevisiae , and detection of interactions between NBA‐containing peptides and T7 phages displaying proteins by both enzyme‐linked immunosorbent assays (ELISA) and label‐free anomalous reflection of gold (AR) measurements. Twenty‐eight phage clones were obtained by the phage‐display method and sequenced. Ten of 28 clones were expected to be nucleic acid‐related proteins including initiation factor, TYB protein, ribosomal proteins, elongation factor, ATP synthase subunit, GTP‐binding protein, and ribonuclease. Other phage clones encoded several classes of enzymes such as reductase, oxidase, aldolase, metalloprotease, and hexokinase. Both ELISA and AR measurements suggested that the methodology of in vitro selection for recognition of the NBA‐containing peptide presented in this study was successfully established. Such a combination of NBA and phage display technologies would be potential to efficiently confirm valuable target proteins binding specifically to capturing agents, to be arrayed onto solid surfaces to develop the designed peptide chip. © 2007 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 88: 131–140, 2007. This article was originally published online as an accepted preprint. The ‘Published Online’ date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com" @default.
• W2044594717 created "2016-06-24" @default.
• W2044594717 creator A5007273317 @default.
• W2044594717 creator A5031934027 @default.
• W2044594717 creator A5053125245 @default.
• W2044594717 creator A5073861733 @default.
• W2044594717 creator A5075155329 @default.
• W2044594717 creator A5083766528 @default.
• W2044594717 date "2007-01-01" @default.
• W2044594717 modified "2023-10-10" @default.
• W2044594717 title "Interactions between peptides containing nucleobase amino acids and T7 phages displayingS. cerevisiae proteins" @default.
• W2044594717 cites W1583500818 @default.
• W2044594717 cites W1647597862 @default.
• W2044594717 cites W1962479889 @default.
• W2044594717 cites W1970023472 @default.
• W2044594717 cites W1977851761 @default.
• W2044594717 cites W1992004901 @default.
• W2044594717 cites W1992632430 @default.
• W2044594717 cites W1997409305 @default.
• W2044594717 cites W2006635085 @default.
• W2044594717 cites W2020451776 @default.
• W2044594717 cites W2022388815 @default.
• W2044594717 cites W2022587307 @default.
• W2044594717 cites W2030836174 @default.
• W2044594717 cites W2032699581 @default.
• W2044594717 cites W2035650745 @default.
• W2044594717 cites W2037523730 @default.
• W2044594717 cites W2046719596 @default.
• W2044594717 cites W2050887290 @default.
• W2044594717 cites W2052046958 @default.
• W2044594717 cites W2052982714 @default.
• W2044594717 cites W2057993402 @default.
• W2044594717 cites W2062937323 @default.
• W2044594717 cites W2063076055 @default.
• W2044594717 cites W2070669937 @default.
• W2044594717 cites W2074691571 @default.
• W2044594717 cites W2074812852 @default.
• W2044594717 cites W2080404655 @default.
• W2044594717 cites W2084183668 @default.
• W2044594717 cites W2087014867 @default.
• W2044594717 cites W2098016095 @default.
• W2044594717 cites W2120810198 @default.
• W2044594717 cites W2128744087 @default.
• W2044594717 cites W2137175516 @default.
• W2044594717 cites W2142531575 @default.
• W2044594717 cites W4255036335 @default.
• W2044594717 cites W76851809 @default.
• W2044594717 doi "https://doi.org/10.1002/bip.20662" @default.
• W2044594717 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17206624" @default.
• W2044594717 hasPublicationYear "2007" @default.
• W2044594717 type Work @default.
• W2044594717 sameAs 2044594717 @default.
• W2044594717 citedByCount "24" @default.
• W2044594717 countsByYear W20445947172012 @default.
• W2044594717 countsByYear W20445947172014 @default.
• W2044594717 countsByYear W20445947172015 @default.
• W2044594717 countsByYear W20445947172016 @default.
• W2044594717 countsByYear W20445947172017 @default.
• W2044594717 countsByYear W20445947172018 @default.
• W2044594717 countsByYear W20445947172019 @default.
• W2044594717 countsByYear W20445947172020 @default.
• W2044594717 countsByYear W20445947172021 @default.
• W2044594717 countsByYear W20445947172022 @default.
• W2044594717 countsByYear W20445947172023 @default.
• W2044594717 crossrefType "journal-article" @default.
• W2044594717 hasAuthorship W2044594717A5007273317 @default.
• W2044594717 hasAuthorship W2044594717A5031934027 @default.
• W2044594717 hasAuthorship W2044594717A5053125245 @default.
• W2044594717 hasAuthorship W2044594717A5073861733 @default.
• W2044594717 hasAuthorship W2044594717A5075155329 @default.
• W2044594717 hasAuthorship W2044594717A5083766528 @default.
• W2044594717 hasBestOaLocation W20445947171 @default.
• W2044594717 hasConcept C104317684 @default.
• W2044594717 hasConcept C104397665 @default.
• W2044594717 hasConcept C185592680 @default.
• W2044594717 hasConcept C186268636 @default.
• W2044594717 hasConcept C24107716 @default.
• W2044594717 hasConcept C2779281246 @default.
• W2044594717 hasConcept C38062823 @default.
• W2044594717 hasConcept C515207424 @default.
• W2044594717 hasConcept C55493867 @default.
• W2044594717 hasConcept C67705224 @default.
• W2044594717 hasConcept C70721500 @default.
• W2044594717 hasConcept C86803240 @default.
• W2044594717 hasConcept C88478588 @default.
• W2044594717 hasConceptScore W2044594717C104317684 @default.
• W2044594717 hasConceptScore W2044594717C104397665 @default.
• W2044594717 hasConceptScore W2044594717C185592680 @default.
• W2044594717 hasConceptScore W2044594717C186268636 @default.
• W2044594717 hasConceptScore W2044594717C24107716 @default.
• W2044594717 hasConceptScore W2044594717C2779281246 @default.
• W2044594717 hasConceptScore W2044594717C38062823 @default.
• W2044594717 hasConceptScore W2044594717C515207424 @default.
• W2044594717 hasConceptScore W2044594717C55493867 @default.
• W2044594717 hasConceptScore W2044594717C67705224 @default.
• W2044594717 hasConceptScore W2044594717C70721500 @default.
• W2044594717 hasConceptScore W2044594717C86803240 @default.
• W2044594717 hasConceptScore W2044594717C88478588 @default.

• next