Matches in SemOpenAlex for { <https://semopenalex.org/work/W2137391369> ?p ?o ?g. }
- W2137391369 endingPage "8139" @default.
- W2137391369 startingPage "8134" @default.
- W2137391369 abstract "These studies explore the role of conformational change and exposed carbohydrate residues in the clearance of alpha 2-macroglobulin-trypsin (alpha 2M-T) complexes in the mouse. Human alpha 2-macroglobulin (alpha 2M) was purified and demonstrated to be homogeneous in the electrophoretic slow form. Two conformationally altered derivatives, alpha 2M-T and alpha 2-macroglobulin-methylamine (alpha 2M-MeNH2), were prepared and demonstrated to exist in the electrophoretic fast form. Radiolabeled alpha 2M-T and alpha 2M-MeNH2 were cleared rapidly with a half-life of 2-4 min following injection into mice. Radiolabeled native alpha 2M, however, remained in the circulation with a half-life of several hours. Both alpha 2M-T and alpha 2M-MeNH2 bound specifically to mouse peritoneal macrophages at 4 degrees C and occupancy of receptor sites increased with increasing time and radioligand concentration. Excess amounts of unlabeled alpha 2M-T or alpha 2M-MeNH2 cross-completed with trace amounts of the other in both clearance studies and binding assays, indicating that both derivatives were removed by the same receptor pathway. The clearance and binding of alpha 2M-T and alpha 2M-MeNH2 were not inhibited by excess amounts of unlabeled asialoorosomucoid, fucosyl-bovine serum albumin, mannosyl-BSA, or N-acetylglucosaminyl-BSA. Our results indicate that the clearance pathway removing alpha 2M-T complexes from the circulation recognizes a fundamental conformational change in alpha 2M secondary to protease binding, which can also be induced by exposure to methylamine. Therefore, other chemical or physical alterations that occur in alpha 2M upon binding trypsin, apart from the conformational change also present in alpha 2M-MeNH2, do not seem necessary for the recognition of alpha 2M-T by cells in the clearance pathway. In addition, this pathway appears distinct from several systems already described mediating clearance of glycoproteins through recognition of terminal galactose, fucose, N-acetylglucosamine, or mannose on oligosaccharide side chains." @default.
- W2137391369 created "2016-06-24" @default.
- W2137391369 creator A5011865676 @default.
- W2137391369 creator A5090928660 @default.
- W2137391369 date "1981-08-01" @default.
- W2137391369 modified "2023-10-01" @default.
- W2137391369 title "Clearance and binding of two electrophoretic “fast” forms of human alpha 2-macroglobulin." @default.
- W2137391369 cites W1514143259 @default.
- W2137391369 cites W1519994409 @default.
- W2137391369 cites W1546458288 @default.
- W2137391369 cites W1559187524 @default.
- W2137391369 cites W1577502833 @default.
- W2137391369 cites W1717442359 @default.
- W2137391369 cites W1758096854 @default.
- W2137391369 cites W1775749144 @default.
- W2137391369 cites W1790158792 @default.
- W2137391369 cites W1893651774 @default.
- W2137391369 cites W1964992614 @default.
- W2137391369 cites W1971865056 @default.
- W2137391369 cites W1978105709 @default.
- W2137391369 cites W1981874508 @default.
- W2137391369 cites W2001167497 @default.
- W2137391369 cites W2003297361 @default.
- W2137391369 cites W2003470884 @default.
- W2137391369 cites W2019524205 @default.
- W2137391369 cites W2028759964 @default.
- W2137391369 cites W2036212754 @default.
- W2137391369 cites W2037258202 @default.
- W2137391369 cites W2044914819 @default.
- W2137391369 cites W2047903470 @default.
- W2137391369 cites W2054941870 @default.
- W2137391369 cites W2059142712 @default.
- W2137391369 cites W2065800083 @default.
- W2137391369 cites W2068934482 @default.
- W2137391369 cites W2074799652 @default.
- W2137391369 cites W2081828201 @default.
- W2137391369 cites W2125748383 @default.
- W2137391369 cites W2212388653 @default.
- W2137391369 cites W2218591063 @default.
- W2137391369 cites W2321822540 @default.
- W2137391369 cites W4247277860 @default.
- W2137391369 doi "https://doi.org/10.1016/s0021-9258(18)43398-4" @default.
- W2137391369 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/6167573" @default.
- W2137391369 hasPublicationYear "1981" @default.
- W2137391369 type Work @default.
- W2137391369 sameAs 2137391369 @default.
- W2137391369 citedByCount "385" @default.
- W2137391369 countsByYear W21373913692012 @default.
- W2137391369 countsByYear W21373913692013 @default.
- W2137391369 countsByYear W21373913692014 @default.
- W2137391369 countsByYear W21373913692015 @default.
- W2137391369 countsByYear W21373913692016 @default.
- W2137391369 countsByYear W21373913692017 @default.
- W2137391369 countsByYear W21373913692018 @default.
- W2137391369 countsByYear W21373913692019 @default.
- W2137391369 countsByYear W21373913692020 @default.
- W2137391369 countsByYear W21373913692021 @default.
- W2137391369 countsByYear W21373913692022 @default.
- W2137391369 countsByYear W21373913692023 @default.
- W2137391369 crossrefType "journal-article" @default.
- W2137391369 hasAuthorship W2137391369A5011865676 @default.
- W2137391369 hasAuthorship W2137391369A5090928660 @default.
- W2137391369 hasBestOaLocation W21373913691 @default.
- W2137391369 hasConcept C104317684 @default.
- W2137391369 hasConcept C159110408 @default.
- W2137391369 hasConcept C185592680 @default.
- W2137391369 hasConcept C2775944032 @default.
- W2137391369 hasConcept C2781054842 @default.
- W2137391369 hasConcept C40250595 @default.
- W2137391369 hasConcept C49453240 @default.
- W2137391369 hasConcept C52543561 @default.
- W2137391369 hasConcept C55493867 @default.
- W2137391369 hasConcept C64943373 @default.
- W2137391369 hasConcept C71924100 @default.
- W2137391369 hasConcept C91238131 @default.
- W2137391369 hasConceptScore W2137391369C104317684 @default.
- W2137391369 hasConceptScore W2137391369C159110408 @default.
- W2137391369 hasConceptScore W2137391369C185592680 @default.
- W2137391369 hasConceptScore W2137391369C2775944032 @default.
- W2137391369 hasConceptScore W2137391369C2781054842 @default.
- W2137391369 hasConceptScore W2137391369C40250595 @default.
- W2137391369 hasConceptScore W2137391369C49453240 @default.
- W2137391369 hasConceptScore W2137391369C52543561 @default.
- W2137391369 hasConceptScore W2137391369C55493867 @default.
- W2137391369 hasConceptScore W2137391369C64943373 @default.
- W2137391369 hasConceptScore W2137391369C71924100 @default.
- W2137391369 hasConceptScore W2137391369C91238131 @default.
- W2137391369 hasIssue "15" @default.
- W2137391369 hasLocation W21373913691 @default.
- W2137391369 hasOpenAccess W2137391369 @default.
- W2137391369 hasPrimaryLocation W21373913691 @default.
- W2137391369 hasRelatedWork W1974500370 @default.
- W2137391369 hasRelatedWork W2001981207 @default.
- W2137391369 hasRelatedWork W2015381079 @default.
- W2137391369 hasRelatedWork W2089774820 @default.
- W2137391369 hasRelatedWork W2412902122 @default.
- W2137391369 hasRelatedWork W2414355290 @default.
- W2137391369 hasRelatedWork W2415646117 @default.