<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>214(3)</volume><submitter>Osborne WR</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><journal>The Biochemical journal</journal><pagination>711-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1152307</full_dataset_link><abstract>Purine nucleoside phosphorylase (NP; EC 2.4.2.1) deficiency is associated with defective T-cell and normal B-cell immunity. Biochemical mechanisms were investigated by measuring deoxyguanosine and guanosine metabolism in normal T and B lymphoblasts and NP-deficient B lymphoblasts. Deoxyguanosine kinase activity was specifically measured by using an anti-NP antibody to prevent alternative-product formation. Kinase activity towards deoxyguanosine was significantly higher in T-cells, whereas NP activity was similar in both B- and T-cells. Only in T-cells was dGTP produced from exogenous deoxyguanosine, and this was prevented by the simultaneous addition of deoxycytidine, which resulted in a concomitant increase in GTP synthesis. Inhibition by 8-aminoguanosine of NP activity in T lymphoblasts increased formation of dGTP and decreased that of GTP from deoxyguanosine and decreased the formation of GTP from guanosine. These data suggest a central role for deoxyguanosine kinase activity in the T-cell selectivity of the immune defect.</abstract><repository>biostudies-other</repository><funding_grant_id>AI-12617</funding_grant_id><funding_grant_id>HL-17265</funding_grant_id><funding_grant_id>GM-15253</funding_grant_id><data_source>Europe PMC</data_source><pubmed_authors>Osborne WR</pubmed_authors><pubmed_authors>Scott CR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The metabolism of deoxyguanosine and guanosine in human B and T lymphoblasts. A role for deoxyguanosine kinase activity in the selective T-cell defect associated with purine nucleoside phosphorylase deficiency.</name><description>Purine nucleoside phosphorylase (NP; EC 2.4.2.1) deficiency is associated with defective T-cell and normal B-cell immunity. Biochemical mechanisms were investigated by measuring deoxyguanosine and guanosine metabolism in normal T and B lymphoblasts and NP-deficient B lymphoblasts. Deoxyguanosine kinase activity was specifically measured by using an anti-NP antibody to prevent alternative-product formation. Kinase activity towards deoxyguanosine was significantly higher in T-cells, whereas NP activity was similar in both B- and T-cells. Only in T-cells was dGTP produced from exogenous deoxyguanosine, and this was prevented by the simultaneous addition of deoxycytidine, which resulted in a concomitant increase in GTP synthesis. Inhibition by 8-aminoguanosine of NP activity in T lymphoblasts increased formation of dGTP and decreased that of GTP from deoxyguanosine and decreased the formation of GTP from guanosine. These data suggest a central role for deoxyguanosine kinase activity in the T-cell selectivity of the immune defect.</description><dates><release>1983-01-01T00:00:00Z</release><publication>1983 Sep</publication><modification>2019-08-04T07:20:14Z</modification><creation>2019-08-04T07:20:14Z</creation></dates><accession>S-EPMC1152307</accession><cross_references/></HashMap>