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Repurposed 3D Printer Allows Economical and Programmable Fraction Collection for Proteomics of Nanogram Scale Samples.
Kitano, Eduardo S; Nisbet, Gareth; Demyanenko, Yana; Kowalczyk, Katarzyna M; Iselin, Louisa; Cross, Stephen; Castello, Alfredo; Mohammed, Shabaz.
Afiliação
  • Kitano ES; Rosalind Franklin Institute, Harwell Campus, Didcot OX11 0QX, United Kingdom.
  • Nisbet G; Department of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.
  • Demyanenko Y; Diamond Light Source, Harwell Science and Innovation Campus, Didcot OX11 0DE, United Kingdom.
  • Kowalczyk KM; Rosalind Franklin Institute, Harwell Campus, Didcot OX11 0QX, United Kingdom.
  • Iselin L; Department of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.
  • Cross S; Rosalind Franklin Institute, Harwell Campus, Didcot OX11 0QX, United Kingdom.
  • Castello A; Department of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.
  • Mohammed S; MRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, United Kingdom.
Anal Chem ; 96(28): 11439-11447, 2024 07 16.
Article em En | MEDLINE | ID: mdl-38968027
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteômica / Impressão Tridimensional Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteômica / Impressão Tridimensional Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article