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Magnetic Synthetic Receptors for Selective Clean-Up in Protein Biomarker Quantification.
McKitterick, Nicholas; Braathen, Frida; Switnicka-Plak, Magdalena A; Cormack, Peter A G; Reubsaet, Léon; Halvorsen, Trine Grønhaug.
Afiliação
  • McKitterick N; Section for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
  • Braathen F; Section for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
  • Switnicka-Plak MA; WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, Scotland, U.K.
  • Cormack PAG; WestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, Scotland, U.K.
  • Reubsaet L; Section for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
  • Halvorsen TG; Section for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
J Proteome Res ; 19(8): 3573-3582, 2020 08 07.
Article em En | MEDLINE | ID: mdl-32614597
ABSTRACT
Biomarker analysis by mass spectrometry (MS) can allow for the rapid quantification of low abundant biomarkers. However, the complexity of human serum is a limiting factor in MS-based bioanalysis; therefore, novel biomarker enrichment strategies are of interest, particularly if the enrichment strategies are of low cost and are easy to use. One such strategy involves the use of molecularly imprinted polymers (MIPs) as synthetic receptors for biomarker enrichment. In the present study, a magnetic solid-phase extraction (mSPE) platform, based on magnetic MIP (mMIP) sorbents, is disclosed, for use in the MS-based quantification of proteins by the bottom-up approach. Progastrin releasing peptide (ProGRP), a low abundant and clinically sensitive biomarker for small cell lung cancer (SCLC), was used to exemplify the mSPE platform. Four different mMIPs were synthesized, and an mSPE method was developed and optimized for the extraction of low concentrations of tryptic peptides from human serum. The mSPE method enabled the selective extraction of the ProGRP signature peptide, the nonapeptide NLLGLIEAK, prior to quantification of the target via LC-MS/MS. Overall, the mSPE method demonstrated its potential as a low cost, rapid, and straightforward sample preparation method, with demonstrably strong binding, acceptable recoveries, and good compatibility with MS. mMIPs are a potential low-cost alternative to current clinical methods for biomarker analysis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Artificiais / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: J Proteome Res Assunto da revista: BIOQUIMICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores Artificiais / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: J Proteome Res Assunto da revista: BIOQUIMICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Noruega