Matches in SemOpenAlex for { <https://semopenalex.org/work/W2163320658> ?p ?o ?g. }
- W2163320658 endingPage "38938" @default.
- W2163320658 startingPage "38932" @default.
- W2163320658 abstract "Bone morphogenetic protein-1 (BMP-1) and the tolloid-like metalloproteinases control several aspects of embryonic development and tissue repair. Unlike other proteinases whose activities are regulated mainly by endogenous inhibitors, regulation of BMP-1/tolloid-like proteinases relies mostly on proteins that stimulate activity. Among these, procollagen C-proteinase enhancers (PCPEs) markedly increase BMP-1/tolloid-like proteinase activity on fibrillar procollagens, in a substrate-specific manner. Here, we performed a detailed quantitative study of the binding of PCPE-1 and of its minimal active fragment (CUB1-CUB2) to three regions of the procollagen III molecule: the triple helix, the C-telopeptide, and the C-propeptide. Contrary to results described elsewhere, we found the PCPE-1-binding sites to be located exclusively in the C-propeptide region. In addition, binding and enhancing activities were found to be independent of the glycosylation state of the C-propeptide. These data exclude previously proposed mechanisms for the action of PCPEs and also suggest new mechanisms to explain how these proteins can stimulate BMP-1/tolloid-like proteinases by up to 20-fold. Bone morphogenetic protein-1 (BMP-1) and the tolloid-like metalloproteinases control several aspects of embryonic development and tissue repair. Unlike other proteinases whose activities are regulated mainly by endogenous inhibitors, regulation of BMP-1/tolloid-like proteinases relies mostly on proteins that stimulate activity. Among these, procollagen C-proteinase enhancers (PCPEs) markedly increase BMP-1/tolloid-like proteinase activity on fibrillar procollagens, in a substrate-specific manner. Here, we performed a detailed quantitative study of the binding of PCPE-1 and of its minimal active fragment (CUB1-CUB2) to three regions of the procollagen III molecule: the triple helix, the C-telopeptide, and the C-propeptide. Contrary to results described elsewhere, we found the PCPE-1-binding sites to be located exclusively in the C-propeptide region. In addition, binding and enhancing activities were found to be independent of the glycosylation state of the C-propeptide. These data exclude previously proposed mechanisms for the action of PCPEs and also suggest new mechanisms to explain how these proteins can stimulate BMP-1/tolloid-like proteinases by up to 20-fold." @default.
- W2163320658 created "2016-06-24" @default.
- W2163320658 creator A5006549290 @default.
- W2163320658 creator A5014967435 @default.
- W2163320658 creator A5049423085 @default.
- W2163320658 creator A5067018409 @default.
- W2163320658 creator A5068553618 @default.
- W2163320658 creator A5071189060 @default.
- W2163320658 creator A5074848089 @default.
- W2163320658 creator A5078668459 @default.
- W2163320658 creator A5080777012 @default.
- W2163320658 creator A5090290848 @default.
- W2163320658 date "2011-11-01" @default.
- W2163320658 modified "2023-10-15" @default.
- W2163320658 title "Procollagen C-proteinase Enhancer Stimulates Procollagen Processing by Binding to the C-propeptide Region Only" @default.
- W2163320658 cites W1517515485 @default.
- W2163320658 cites W1563393647 @default.
- W2163320658 cites W1649327708 @default.
- W2163320658 cites W1966078729 @default.
- W2163320658 cites W1968263279 @default.
- W2163320658 cites W1970846696 @default.
- W2163320658 cites W1981269419 @default.
- W2163320658 cites W1984011890 @default.
- W2163320658 cites W1987916005 @default.
- W2163320658 cites W1992203325 @default.
- W2163320658 cites W1997516024 @default.
- W2163320658 cites W2001614649 @default.
- W2163320658 cites W2002979335 @default.
- W2163320658 cites W2009869955 @default.
- W2163320658 cites W2013180323 @default.
- W2163320658 cites W2024862693 @default.
- W2163320658 cites W2027440025 @default.
- W2163320658 cites W2028723084 @default.
- W2163320658 cites W2030744682 @default.
- W2163320658 cites W2032274963 @default.
- W2163320658 cites W2040446257 @default.
- W2163320658 cites W2040479916 @default.
- W2163320658 cites W2041966195 @default.
- W2163320658 cites W2044615295 @default.
- W2163320658 cites W2061963189 @default.
- W2163320658 cites W2072008893 @default.
- W2163320658 cites W2072158996 @default.
- W2163320658 cites W2076947779 @default.
- W2163320658 cites W2085465381 @default.
- W2163320658 cites W2093395445 @default.
- W2163320658 cites W2093879310 @default.
- W2163320658 cites W2094727741 @default.
- W2163320658 cites W2098336957 @default.
- W2163320658 cites W2113890602 @default.
- W2163320658 cites W2124492445 @default.
- W2163320658 cites W2127943442 @default.
- W2163320658 cites W2132764926 @default.
- W2163320658 cites W2157845321 @default.
- W2163320658 cites W2162568753 @default.
- W2163320658 cites W2163785113 @default.
- W2163320658 cites W2164762331 @default.
- W2163320658 cites W2166815562 @default.
- W2163320658 cites W2167413619 @default.
- W2163320658 doi "https://doi.org/10.1074/jbc.m111.274944" @default.
- W2163320658 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3234718" @default.
- W2163320658 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21940633" @default.
- W2163320658 hasPublicationYear "2011" @default.
- W2163320658 type Work @default.
- W2163320658 sameAs 2163320658 @default.
- W2163320658 citedByCount "43" @default.
- W2163320658 countsByYear W21633206582012 @default.
- W2163320658 countsByYear W21633206582013 @default.
- W2163320658 countsByYear W21633206582014 @default.
- W2163320658 countsByYear W21633206582015 @default.
- W2163320658 countsByYear W21633206582016 @default.
- W2163320658 countsByYear W21633206582017 @default.
- W2163320658 countsByYear W21633206582018 @default.
- W2163320658 countsByYear W21633206582019 @default.
- W2163320658 countsByYear W21633206582020 @default.
- W2163320658 countsByYear W21633206582021 @default.
- W2163320658 countsByYear W21633206582022 @default.
- W2163320658 crossrefType "journal-article" @default.
- W2163320658 hasAuthorship W2163320658A5006549290 @default.
- W2163320658 hasAuthorship W2163320658A5014967435 @default.
- W2163320658 hasAuthorship W2163320658A5049423085 @default.
- W2163320658 hasAuthorship W2163320658A5067018409 @default.
- W2163320658 hasAuthorship W2163320658A5068553618 @default.
- W2163320658 hasAuthorship W2163320658A5071189060 @default.
- W2163320658 hasAuthorship W2163320658A5074848089 @default.
- W2163320658 hasAuthorship W2163320658A5078668459 @default.
- W2163320658 hasAuthorship W2163320658A5080777012 @default.
- W2163320658 hasAuthorship W2163320658A5090290848 @default.
- W2163320658 hasBestOaLocation W21633206581 @default.
- W2163320658 hasConcept C104317684 @default.
- W2163320658 hasConcept C109523444 @default.
- W2163320658 hasConcept C111936080 @default.
- W2163320658 hasConcept C150194340 @default.
- W2163320658 hasConcept C153911025 @default.
- W2163320658 hasConcept C181199279 @default.
- W2163320658 hasConcept C185592680 @default.
- W2163320658 hasConcept C31507581 @default.
- W2163320658 hasConcept C55493867 @default.
- W2163320658 hasConcept C55728118 @default.