<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>100(7)</volume><submitter>Kimura E</submitter><pubmed_abstract>Our originally designed dansylamidoethylcyclen 4 as a biomimetic Zn(2+)-selective fluorophore has been demonstrated to be a good detector of the apoptosis (induced by an anticancer agent, etoposide, and H(2)O(2)) in cancer cells such as HeLa and HL60 cells. The macrocyclic Zn(2+) ligand 4 (mostly as a deprotonated form) is cell-permeable to show weak fluorescence (emission at 550 nm), which forms a strong fluorescent 1:1 Zn(2+) complex 5 (emission at 530 nm) when Zn(2+) is incorporated into the cells by a zinc(II) ionophore pyrithione. Thus formed, Zn(2+) complex 5 is cell-impermeable and remains intact over a few hours. When apoptosis in HeLa or HL60 cells is artificially induced, 4 selectively and strongly stains apoptotic cells only at early stages, which was verified by using the conventional apoptosis detection probe annexin V-Cy3. Detection of the apoptotic cells by 4 was perhaps due to significantly increased free Zn(2+) flux at early stages of apoptosis. Apoptotic detection by 4 has been compared with a presently available Zn(2+) fluorophore, Zinquin 1. We present that 4 has advantages in detection of apoptosis over annexin V-Cy3 and Zinquin 1.</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>3731-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC152990</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A macrocyclic zinc(II) fluorophore as a detector of apoptosis.</pubmed_title><pmcid>PMC152990</pmcid><pubmed_authors>Koike T</pubmed_authors><pubmed_authors>Kimura E</pubmed_authors><pubmed_authors>Aoki S</pubmed_authors><pubmed_authors>Kikuta E</pubmed_authors></additional><is_claimable>false</is_claimable><name>A macrocyclic zinc(II) fluorophore as a detector of apoptosis.</name><description>Our originally designed dansylamidoethylcyclen 4 as a biomimetic Zn(2+)-selective fluorophore has been demonstrated to be a good detector of the apoptosis (induced by an anticancer agent, etoposide, and H(2)O(2)) in cancer cells such as HeLa and HL60 cells. The macrocyclic Zn(2+) ligand 4 (mostly as a deprotonated form) is cell-permeable to show weak fluorescence (emission at 550 nm), which forms a strong fluorescent 1:1 Zn(2+) complex 5 (emission at 530 nm) when Zn(2+) is incorporated into the cells by a zinc(II) ionophore pyrithione. Thus formed, Zn(2+) complex 5 is cell-impermeable and remains intact over a few hours. When apoptosis in HeLa or HL60 cells is artificially induced, 4 selectively and strongly stains apoptotic cells only at early stages, which was verified by using the conventional apoptosis detection probe annexin V-Cy3. Detection of the apoptotic cells by 4 was perhaps due to significantly increased free Zn(2+) flux at early stages of apoptosis. Apoptotic detection by 4 has been compared with a presently available Zn(2+) fluorophore, Zinquin 1. We present that 4 has advantages in detection of apoptosis over annexin V-Cy3 and Zinquin 1.</description><dates><release>2003-01-01T00:00:00Z</release><publication>2003 Apr</publication><modification>2024-11-10T08:00:26.825Z</modification><creation>2019-03-27T00:17:42Z</creation></dates><accession>S-EPMC152990</accession><cross_references><pubmed>12646703</pubmed><doi>10.1073/pnas.0637275100</doi></cross_references></HashMap>