<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>55</viewCount><searchCount>0</searchCount></scores><additional><submitter>Gopinath T</submitter><funding>American Heart Association</funding><funding>NHLBI NIH HHS</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>267-285</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7236978</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(4-5)</volume><pubmed_abstract>Ultrafast magic angle spinning (MAS) technology and &lt;sup>1&lt;/sup>H detection have dramatically enhanced the sensitivity of solid-state NMR (ssNMR) spectroscopy of biopolymers. We previously showed that, when combined with polarization optimized experiments (POE), these advancements enable the simultaneous acquisition of multi-dimensional &lt;sup>1&lt;/sup>H- or &lt;sup>13&lt;/sup>C-detected experiments using a single receiver. Here, we propose a new sub-class within the POE family, namely HC-DUMAS, HC-MEIOSIS, and HC-MAeSTOSO, that utilize dual receiver technology for the simultaneous detection of &lt;sup>1&lt;/sup>H and &lt;sup>13&lt;/sup>C nuclei. We also expand this approach to record &lt;sup>1&lt;/sup>H-, &lt;sup>13&lt;/sup>C-, and &lt;sup>15&lt;/sup>N-detected homonuclear 2D spectra simultaneously using three independent receivers. The combination of POE and multi-receiver technology will further shorten the total experimental time of ssNMR experiments for biological solids.</pubmed_abstract><journal>Journal of biomolecular NMR</journal><pubmed_title>Multi-receiver solid-state NMR using polarization optimized experiments (POE) at ultrafast magic angle spinning.</pubmed_title><pmcid>PMC7236978</pmcid><funding_grant_id>1S10OD021536</funding_grant_id><funding_grant_id>GM 64742</funding_grant_id><funding_grant_id>R01 GM064742</funding_grant_id><funding_grant_id>S10 OD021536</funding_grant_id><funding_grant_id>R01 HL144130</funding_grant_id><funding_grant_id>HL 144130</funding_grant_id><funding_grant_id>19POST34420009</funding_grant_id><pubmed_authors>Gopinath T</pubmed_authors><pubmed_authors>Veglia G</pubmed_authors><pubmed_authors>Weber DK</pubmed_authors><view_count>55</view_count></additional><is_claimable>false</is_claimable><name>Multi-receiver solid-state NMR using polarization optimized experiments (POE) at ultrafast magic angle spinning.</name><description>Ultrafast magic angle spinning (MAS) technology and &lt;sup>1&lt;/sup>H detection have dramatically enhanced the sensitivity of solid-state NMR (ssNMR) spectroscopy of biopolymers. We previously showed that, when combined with polarization optimized experiments (POE), these advancements enable the simultaneous acquisition of multi-dimensional &lt;sup>1&lt;/sup>H- or &lt;sup>13&lt;/sup>C-detected experiments using a single receiver. Here, we propose a new sub-class within the POE family, namely HC-DUMAS, HC-MEIOSIS, and HC-MAeSTOSO, that utilize dual receiver technology for the simultaneous detection of &lt;sup>1&lt;/sup>H and &lt;sup>13&lt;/sup>C nuclei. We also expand this approach to record &lt;sup>1&lt;/sup>H-, &lt;sup>13&lt;/sup>C-, and &lt;sup>15&lt;/sup>N-detected homonuclear 2D spectra simultaneously using three independent receivers. The combination of POE and multi-receiver technology will further shorten the total experimental time of ssNMR experiments for biological solids.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2022-02-09T18:08:56.963Z</modification><creation>2022-02-09T18:08:56.963Z</creation></dates><accession>S-EPMC7236978</accession><cross_references><pubmed>32333193</pubmed><doi>10.1007/s10858-020-00316-y</doi></cross_references></HashMap>