Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples
In this work, we describe the construction and application of a repurposed 3D-printer as a fraction collector. We utilize a nano-LC to ensure minimal volumes and surfaces although any LC can be coupled. The setup operates as a high-pH fractionation system capable of effectively working with nanogram...
| Main Authors: | , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
American Chemical Society
2024
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| _version_ | 1826313521544036352 |
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| author | Kitano, ES Nisbet, G Demyanenko, Y Kowalczyk, KM Iselin, L Cross, S Castello, A Mohammed, S |
| author_facet | Kitano, ES Nisbet, G Demyanenko, Y Kowalczyk, KM Iselin, L Cross, S Castello, A Mohammed, S |
| author_sort | Kitano, ES |
| collection | OXFORD |
| description | In this work, we describe the construction and application of a repurposed 3D-printer as a fraction collector. We utilize a nano-LC to ensure minimal volumes and surfaces although any LC can be coupled. The setup operates as a high-pH fractionation system capable of effectively working with nanogram scales of lysate digests. The 2D RP–RP system demonstrated superior proteome coverage over single-shot data-dependent acquisition (DDA) analysis using only 5 ng of human cell lysate digest with performance increasing with increasing amounts of material. We found that the fractionation system allowed over 60% signal recovery at the peptide level and, more importantly, we observed improved protein level intensity coverage, which indicates the complexity reduction afforded by the system outweighs the sample losses endured. The application of data-independent acquisition (DIA) and wide window acquisition (WWA) to fractionated samples allowed nearly 8000 proteins to be identified from 50 ng of the material. The utility of the 2D system was further investigated for phosphoproteomics (>21 000 phosphosites from 50 μg starting material) and pull-down type experiments and showed substantial improvements over single-shot experiments. We show that the 2D RP–RP system is a highly versatile and powerful tool for many proteomics workflows. |
| first_indexed | 2024-09-25T04:15:23Z |
| format | Journal article |
| id | oxford-uuid:5bfd010d-a84d-4045-abaf-6d5016a749bb |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-09-25T04:15:23Z |
| publishDate | 2024 |
| publisher | American Chemical Society |
| record_format | dspace |
| spelling | oxford-uuid:5bfd010d-a84d-4045-abaf-6d5016a749bb2024-07-17T20:10:55ZRepurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale SamplesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5bfd010d-a84d-4045-abaf-6d5016a749bbEnglishJisc Publications RouterAmerican Chemical Society2024Kitano, ESNisbet, GDemyanenko, YKowalczyk, KMIselin, LCross, SCastello, AMohammed, SIn this work, we describe the construction and application of a repurposed 3D-printer as a fraction collector. We utilize a nano-LC to ensure minimal volumes and surfaces although any LC can be coupled. The setup operates as a high-pH fractionation system capable of effectively working with nanogram scales of lysate digests. The 2D RP–RP system demonstrated superior proteome coverage over single-shot data-dependent acquisition (DDA) analysis using only 5 ng of human cell lysate digest with performance increasing with increasing amounts of material. We found that the fractionation system allowed over 60% signal recovery at the peptide level and, more importantly, we observed improved protein level intensity coverage, which indicates the complexity reduction afforded by the system outweighs the sample losses endured. The application of data-independent acquisition (DIA) and wide window acquisition (WWA) to fractionated samples allowed nearly 8000 proteins to be identified from 50 ng of the material. The utility of the 2D system was further investigated for phosphoproteomics (>21 000 phosphosites from 50 μg starting material) and pull-down type experiments and showed substantial improvements over single-shot experiments. We show that the 2D RP–RP system is a highly versatile and powerful tool for many proteomics workflows. |
| spellingShingle | Kitano, ES Nisbet, G Demyanenko, Y Kowalczyk, KM Iselin, L Cross, S Castello, A Mohammed, S Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title | Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title_full | Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title_fullStr | Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title_full_unstemmed | Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title_short | Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples |
| title_sort | repurposed 3d printer allows economical and programmable fraction collection for proteomics of nanogram scale samples |
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