<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Porat-Dahlerbruch G</submitter><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIAID</funding><pagination>107649</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11031345</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>361</volume><pubmed_abstract>Biomolecular solid-state magic angle spinning (MAS) NMR spectroscopy frequently relies on selective &lt;sup>13&lt;/sup>C-&lt;sup>15&lt;/sup>N magnetization transfers, for various kinds of correlation experiments. Introduced in 1998, spectrally induced filtering in combination with cross polarization (SPECIFIC-CP) is a selective heteronuclear magnetization transfer experiment widely used for biological applications. At MAS frequencies below 20 kHz, commonly used for &lt;sup>13&lt;/sup>C-detected MAS NMR experiments, SPECIFIC-CP transfer between amide &lt;sup>15&lt;/sup>N and &lt;sup>13&lt;/sup>C&lt;sup>α&lt;/sup> atoms (NCA) is typically performed with radiofrequency (rf) fields set higher than the MAS frequency for both &lt;sup>13&lt;/sup>C and &lt;sup>15&lt;/sup>N channels, and high-power &lt;sup>1&lt;/sup>H decoupling rf field is simultaneously applied. Here, we experimentally explore a broad range of NCA zero-quantum (ZQ) SPECIFIC-CP matching conditions at the MAS frequency of 14 kHz and compare the best high- and low-power matching conditions with respect to selectivity, robustness, and sensitivity at lower &lt;sup>1&lt;/sup>H decoupling rf fields. We show that low-power NCA SPECIFIC-CP matching condition gives rise to 20% sensitivity enhancement compared to high-power conditions, in 2D NCA spectra of microcrystalline assemblies of HIV-1 CA&lt;sub>CTD&lt;/sub>-SP1 protein with inositol hexakis-phosphate (IP6).</pubmed_abstract><journal>Journal of magnetic resonance (San Diego, Calif. : 1997)</journal><pubmed_title>High-efficiency low-power &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;C-&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N cross polarization in MAS NMR.</pubmed_title><pmcid>PMC11031345</pmcid><funding_grant_id>U54 AI170791</funding_grant_id><funding_grant_id>U54AI170791</funding_grant_id><pubmed_authors>Polenova T</pubmed_authors><pubmed_authors>Porat-Dahlerbruch G</pubmed_authors><pubmed_authors>Struppe J</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-efficiency low-power &amp;lt;sup&amp;gt;13&amp;lt;/sup&amp;gt;C-&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N cross polarization in MAS NMR.</name><description>Biomolecular solid-state magic angle spinning (MAS) NMR spectroscopy frequently relies on selective &lt;sup>13&lt;/sup>C-&lt;sup>15&lt;/sup>N magnetization transfers, for various kinds of correlation experiments. Introduced in 1998, spectrally induced filtering in combination with cross polarization (SPECIFIC-CP) is a selective heteronuclear magnetization transfer experiment widely used for biological applications. At MAS frequencies below 20 kHz, commonly used for &lt;sup>13&lt;/sup>C-detected MAS NMR experiments, SPECIFIC-CP transfer between amide &lt;sup>15&lt;/sup>N and &lt;sup>13&lt;/sup>C&lt;sup>α&lt;/sup> atoms (NCA) is typically performed with radiofrequency (rf) fields set higher than the MAS frequency for both &lt;sup>13&lt;/sup>C and &lt;sup>15&lt;/sup>N channels, and high-power &lt;sup>1&lt;/sup>H decoupling rf field is simultaneously applied. Here, we experimentally explore a broad range of NCA zero-quantum (ZQ) SPECIFIC-CP matching conditions at the MAS frequency of 14 kHz and compare the best high- and low-power matching conditions with respect to selectivity, robustness, and sensitivity at lower &lt;sup>1&lt;/sup>H decoupling rf fields. We show that low-power NCA SPECIFIC-CP matching condition gives rise to 20% sensitivity enhancement compared to high-power conditions, in 2D NCA spectra of microcrystalline assemblies of HIV-1 CA&lt;sub>CTD&lt;/sub>-SP1 protein with inositol hexakis-phosphate (IP6).</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-07-02T03:04:47.736Z</modification><creation>2025-07-02T03:04:47.736Z</creation></dates><accession>S-EPMC11031345</accession><cross_references><pubmed>38452523</pubmed><doi>10.1016/j.jmr.2024.107649</doi></cross_references></HashMap>