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Successive Multiple Ionic-Polymer Layer (SMIL) Coatings for intact protein analysis by Capillary Zone Electrophoresis -Mass Spectrometry -Application to Hemoglobin Analysis

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  • معلومة اضافية
    • Contributors:
      Helmholtz Zentrum München = German Research Center for Environmental Health (HMGU); Aalen University - Hochschule Aalen; Institut des Biomolécules Max Mousseron Pôle Chimie Balard (IBMM); Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM); Université de Montpellier (UM); Christian Neusüß; Kevin Jooß; ANR-20-CE92-0021,SMIL E,Nouveaux revêtements ioniques mutlicouches pour les séparations ultra-efficaces, limitées par la diffusion, de protéines intactes par électrophorèse capillaire et son couplage à la spectrométrie de masse(2020)
    • بيانات النشر:
      HAL CCSD
      Springer US
    • الموضوع:
      2022
    • Collection:
      Université de Montpellier: HAL
    • نبذة مختصرة :
      International audience ; Adsorption of analytes, e.g., proteins, often interfere with separation in CE, due to the relatively large surface of the narrow capillary. Coatings often are applied to prevent adsorption and to determine the electroosmotic flow (EOF), which is of major importance for the separation in CE. Successive multiple ionic-polymer layer (SMIL) coatings are frequently used for protein analysis in capillary electrophoresis resulting in high separation efficiency and repeatability. Here, the coating procedure of a five-layer SMIL coating is described using quaternized diethylaminoethyl dextran (DEAEDq) as polycation and poly(methacrylic acid) (PMA) as polyanion. Depending on the analyte, different polyions may be used to increase separation efficiency. However, the coating procedure remains the same.To demonstrate the applicability of SMIL coatings in CE-MS, human hemoglobin was measured in a BGE containing 2 M acetic acid. DEAEDq-PMA coating was found to be the most suitable for hemoglobin analysis due to relatively low reversed electroosmotic mobility leading to increased electrophoretic resolution of closely related proteoforms. Thereby, not only alpha and beta subunit of the hemoglobin could be separated, but also positional isoforms of glycated and carbamylated species were separated within 24 min.
    • الرقم المعرف:
      10.1007/978-1-0716-2493-7_5
    • الدخول الالكتروني :
      https://hal.science/hal-04605820
      https://hal.science/hal-04605820v1/document
      https://hal.science/hal-04605820v1/file/Buchkapitel_SMIL.pdf
      https://doi.org/10.1007/978-1-0716-2493-7_5
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.B41D16C5