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Characterization of large intact protein ions by mass spectrometry: What directions should we follow?
Fornelli, Luca; Toby, Timothy K.
Afiliación
  • Fornelli L; University of Oklahoma, Department of Biology, 730 Van Vleet oval, Norman, OK 73109, United States of America; University of Oklahoma, Department Chemistry and Biochemistry, 101 Stephenson Parkway, Norman, OK 73109, United States of America. Electronic address: luca.fornelli@ou.edu.
  • Toby TK; DiscernDx, 2478 Embarcadero Way, Palo Alto, CA 94303, United States of America.
Biochim Biophys Acta Proteins Proteom ; 1870(4): 140758, 2022 04 01.
Article en En | MEDLINE | ID: mdl-35077914
ABSTRACT
Theoretically, the gas-phase interrogation of whole proteoforms via mass spectrometry, known as top-down proteomics, bypasses the protein inference problem that afflicts peptide-centric proteomic approaches. Despite this obvious advantage, the application of top-down proteomics remains rare, mainly due to limited throughput and difficulty of analyzing proteins >30 kDa. Here we will discuss some of the problems encountered during the characterization of large proteoforms, and guided by a combination of theoretical background and experimental evidence we will describe some innovative data acquisition strategies and novel mass spectrometry technologies that can at least partially overcome such limitations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Proteómica Idioma: En Revista: Biochim Biophys Acta Proteins Proteom Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Proteómica Idioma: En Revista: Biochim Biophys Acta Proteins Proteom Año: 2022 Tipo del documento: Article