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        <gco:CharacterString>Dataset Description: &amp;lt;p&amp;gt;Related data table and dataset descriptions:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Total spectral counts refer to the total number of spectra with peptide to spectrum matches (PSMs) that matches to each entry within the FASTA sequence database. This approach allows each peptide to map to multiple closely related sequences. In contrast, with exclusive spectral counts each peptide is only allowed to map to one sequence within the FASTA database, and when a peptide is found in multiple database sequences the one with the most peptides mapping (parsimony) to it is selected. There are pros and cons to each approach, where total spectral counts will double count peptides when two similar proteins are compared, and exclusive spectral counts will underrepresent less abundant proteins with shared peptides, favoring the most homolog with the most shared peptides. Considering protein groups with shared peptides or focusing on peptide-level analyses are alternative approaches that could be constructed from these results.&amp;amp;nbsp;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;See &amp;quot;Related Datasets&amp;quot; section for:&amp;lt;br /&amp;gt;
*&amp;amp;nbsp; &amp;quot;AE1913 Protein Spectral Counts&amp;quot; which includes the exclusive and total spectral counts associated with proteins.&amp;lt;br /&amp;gt;
* &amp;quot;AE1913 Protein Identification FASTA&amp;quot;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;CTD and other data from the same cruise are listed on deployment page AE1913: https://www.bco-dmo.org/deployment/916412&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;These data will become part of the Ocean Protein Portal (https://proteinportal.whoi.edu/; Saito et al., 2020).&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Methods are reported in Cohen et al. 2023 (biorxiv preprint doi: &amp;lt;a href=&amp;quot;http://doi.org/10.1101/2023.11.20.567900&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;10.1101/2023.11.20.567900&amp;lt;/a&amp;gt;) and are summarized below.&amp;lt;br /&amp;gt;
* This section describes how this and related datasets were generated (see &amp;quot;Related Datasets&amp;quot; section).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;One half of the 142 mm filters (0.2-51 μm) collected by Clio were processed for metaproteomics. Proteins were extracted in an 1% SDS-based detergent in 50 mM HEPES at pH 8.5, reduced with dithiothreitol, alkylated with iodoacetamide, and purified using a polyacrylamide electrophoresis tube gel method. Protein quantification was performed using a BSA assay. Trypsin was added to the protein-bead mixture in a 1:20 trypsin:protein ratio. Peptides were purified using C18 tips and diluted to a concentration of 0.1 μg μL−1.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Approximately 2-5 µg of purified peptides were injected onto a Dionex UltiMate 3000 RSLCnano LC system with an additional RSLCnano pump, run in online 2D active modulation mode interfaced with a Thermo Fusion mass spectrometer. The mass spectrometer acquired MS1 scans from 380 to 1,580 m/z at 240K resolution in the Orbitrap. MS2 were collected in data dependent mode in the ion trap with a cycle time of 2 seconds between scans and acquisition of charge states 2 to 10. MS2 scans had 1.6 m/z isolation window, 50 ms maximum injection time and 5 s dynamic exclusion time.&amp;amp;nbsp;&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/765944.rdf" xlink:title="OCE-1658030" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1658030 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1658030</gmx:Anchor>
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