4.5 Review

Seeing the complete picture: proteins in top-down mass spectrometry

Journal

ESSAYS IN BIOCHEMISTRY
Volume 67, Issue 2, Pages 283-300

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/EBC20220098

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Top-down protein mass spectrometry provides valuable insights into protein sequence and structure, allowing for precise proteoform identification and the study of protein-ligand and protein-protein interactions. This method differs from traditional bottom-up approaches by analyzing intact proteins instead of digested peptides. This review provides an overview of top-down protein mass spectrometry experiments and highlights recent applications. Various experimental designs are recommended depending on whether sequence information or structural information is prioritized, as well as considerations of solution conditions and sample complexity.
Top-down protein mass spectrometry can provide unique insights into protein sequence and structure, including precise proteoform identification and study of protein-ligand and protein-protein interactions. In contrast with the commonly applied bottom-up approach, top-down approaches do not include digestion of the protein of interest into small peptides, but instead rely on the ionization and subsequent fragmentation of intact proteins. As such, it is fundamentally the only way to fully characterize the composition of a proteoform. Here, we provide an overview of how a top-down protein mass spectrometry experiment is performed and point out recent applications from the literature to the reader. While some parts of the top-down workflow are broadly applicable, different research questions are best addressed with specific experimental designs. The most important divide is between studies that prior-itize sequence information (i.e., proteoform identification) versus structural information (e.g., conformational studies, or mapping protein-protein or protein-ligand interactions). Another important consideration is whether to work under native or denaturing solution conditions, and the overall complexity of the sample also needs to be taken into account, as it deter-mines whether (chromatographic) separation is required prior to MS analysis. In this review, we aim to provide enough information to support both newcomers and more experienced readers in the decision process of how to answer a potential research question most effi-ciently and to provide an overview of the methods that exist to answer these questions.

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