Matches in SemOpenAlex for { <https://semopenalex.org/work/W2025528306> ?p ?o ?g. }
- W2025528306 endingPage "10359" @default.
- W2025528306 startingPage "10355" @default.
- W2025528306 abstract "The binding site in G-protein-linked neurotransmitter receptors is formed among their membrane-spanning segments. Because the binding site is in the plane of the bilayer and is accessible to charged, water-soluble agonists, it must lie in a crevice open to the extracellular, aqueous medium. Information about the structure of these receptors can be obtained by identifying the residues in the membrane-spanning segments which face this water-filled crevice. Human D2 dopamine receptor was expressed in human embryonic kidney 293 cells. Small, charged, sulfhydryl-specific methanethiosulfonate (MTS) derivatives irreversibly inhibited the binding of the D2-specific antagonist [3H]YM-09151-2 to these cells. The highly polar MTS derivatives should react with cysteine sulfhydryl groups only at the water-accessible surface of the receptor, which includes the surface of the binding-site crevice. In contrast, these reagents will have little access to sulfhydryls facing the lipid bilayer or buried in the protein interior. Positively charged MTS reagents irreversibly inhibited binding several hundredfold faster than a negatively charged MTS reagent, consistent with the affinity of the binding site for positively charged dopamine agonists and antagonists. Furthermore, both agonists and antagonists of the D2 receptor protected against irreversible inhibition by the MTS reagents. To identify the susceptible cysteine, we mutated, one at a time, five transmembrane and two extracellular cysteine residues to serine. Only the mutation of Cys118 to serine decreased the susceptibility of antagonist binding to irreversible inhibition by the MTS reagents. Thus, Cys118, a residue in the middle of the third membrane-spanning segment, is exposed in the D2 receptor binding-site crevice." @default.
- W2025528306 created "2016-06-24" @default.
- W2025528306 creator A5004944388 @default.
- W2025528306 creator A5008291982 @default.
- W2025528306 creator A5032077091 @default.
- W2025528306 creator A5076865147 @default.
- W2025528306 date "1994-10-25" @default.
- W2025528306 modified "2023-10-06" @default.
- W2025528306 title "A cysteine residue in the third membrane-spanning segment of the human D2 dopamine receptor is exposed in the binding-site crevice." @default.
- W2025528306 cites W1445935732 @default.
- W2025528306 cites W1479710013 @default.
- W2025528306 cites W1502005164 @default.
- W2025528306 cites W1549134654 @default.
- W2025528306 cites W1573477538 @default.
- W2025528306 cites W1574744729 @default.
- W2025528306 cites W1584684122 @default.
- W2025528306 cites W1654237604 @default.
- W2025528306 cites W1880336884 @default.
- W2025528306 cites W1955225173 @default.
- W2025528306 cites W1966092598 @default.
- W2025528306 cites W1972035961 @default.
- W2025528306 cites W1978850926 @default.
- W2025528306 cites W1978854127 @default.
- W2025528306 cites W1983358193 @default.
- W2025528306 cites W1984918402 @default.
- W2025528306 cites W1993620919 @default.
- W2025528306 cites W1994522080 @default.
- W2025528306 cites W1999653674 @default.
- W2025528306 cites W2001406669 @default.
- W2025528306 cites W2023750079 @default.
- W2025528306 cites W2026395566 @default.
- W2025528306 cites W2027997279 @default.
- W2025528306 cites W2030118669 @default.
- W2025528306 cites W2037992892 @default.
- W2025528306 cites W2059230444 @default.
- W2025528306 cites W2069537899 @default.
- W2025528306 cites W2079463706 @default.
- W2025528306 cites W2080660796 @default.
- W2025528306 cites W2083225580 @default.
- W2025528306 cites W2116949924 @default.
- W2025528306 cites W2129052308 @default.
- W2025528306 cites W2144290901 @default.
- W2025528306 cites W2166217068 @default.
- W2025528306 cites W2319541300 @default.
- W2025528306 cites W2418112607 @default.
- W2025528306 cites W2426254068 @default.
- W2025528306 cites W35264894 @default.
- W2025528306 doi "https://doi.org/10.1073/pnas.91.22.10355" @default.
- W2025528306 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/45018" @default.
- W2025528306 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7937955" @default.
- W2025528306 hasPublicationYear "1994" @default.
- W2025528306 type Work @default.
- W2025528306 sameAs 2025528306 @default.
- W2025528306 citedByCount "115" @default.
- W2025528306 countsByYear W20255283062012 @default.
- W2025528306 countsByYear W20255283062013 @default.
- W2025528306 countsByYear W20255283062014 @default.
- W2025528306 countsByYear W20255283062015 @default.
- W2025528306 countsByYear W20255283062017 @default.
- W2025528306 countsByYear W20255283062018 @default.
- W2025528306 countsByYear W20255283062019 @default.
- W2025528306 countsByYear W20255283062021 @default.
- W2025528306 countsByYear W20255283062022 @default.
- W2025528306 crossrefType "journal-article" @default.
- W2025528306 hasAuthorship W2025528306A5004944388 @default.
- W2025528306 hasAuthorship W2025528306A5008291982 @default.
- W2025528306 hasAuthorship W2025528306A5032077091 @default.
- W2025528306 hasAuthorship W2025528306A5076865147 @default.
- W2025528306 hasBestOaLocation W20255283062 @default.
- W2025528306 hasConcept C104317684 @default.
- W2025528306 hasConcept C107824862 @default.
- W2025528306 hasConcept C12554922 @default.
- W2025528306 hasConcept C149011108 @default.
- W2025528306 hasConcept C170493617 @default.
- W2025528306 hasConcept C181199279 @default.
- W2025528306 hasConcept C185592680 @default.
- W2025528306 hasConcept C2776414213 @default.
- W2025528306 hasConcept C2776755682 @default.
- W2025528306 hasConcept C2779201268 @default.
- W2025528306 hasConcept C2909816965 @default.
- W2025528306 hasConcept C55493867 @default.
- W2025528306 hasConcept C86803240 @default.
- W2025528306 hasConceptScore W2025528306C104317684 @default.
- W2025528306 hasConceptScore W2025528306C107824862 @default.
- W2025528306 hasConceptScore W2025528306C12554922 @default.
- W2025528306 hasConceptScore W2025528306C149011108 @default.
- W2025528306 hasConceptScore W2025528306C170493617 @default.
- W2025528306 hasConceptScore W2025528306C181199279 @default.
- W2025528306 hasConceptScore W2025528306C185592680 @default.
- W2025528306 hasConceptScore W2025528306C2776414213 @default.
- W2025528306 hasConceptScore W2025528306C2776755682 @default.
- W2025528306 hasConceptScore W2025528306C2779201268 @default.
- W2025528306 hasConceptScore W2025528306C2909816965 @default.
- W2025528306 hasConceptScore W2025528306C55493867 @default.
- W2025528306 hasConceptScore W2025528306C86803240 @default.
- W2025528306 hasIssue "22" @default.
- W2025528306 hasLocation W20255283061 @default.
- W2025528306 hasLocation W20255283062 @default.