Literature DB >> 29582994

Analytical Cascades of Enzymes for Sensitive Detection of Structural Variations in Protein Samples.

Julia C Hollerweger1,2, Isabel J Hoppe1,2, Christof Regl1,2, Lorenz G Stock1,2, Christian G Huber1,2, Urs Lohrig2,3, Hanno Stutz1,2, Hans Brandstetter1,2.   

Abstract

Protein function critically depends on structure. However, current analytical tools to monitor consistent higher-order structure with high sensitivity, as for instance required in the development of biopharmaceuticals, are limited. To complement existing assays, we present the analytical cascade of enzymes (ACE), a method based on enzymatic modifications of target proteins, which serve to exponentially amplify structural differences between them. The method enables conformational and chemical fingerprinting of closely related proteins, allowing for the sensitive detection of heterogeneities in protein preparations with high precision. Using this method, we detect protein variants differing in conformation only, as well as structural changes induced by diverse covalent modifications. Additionally, we employ this method to identify the nature of structural variants. Moreover, the ACE method should help to address the limited reproducibility in fundamental research, which partly relates to sample heterogeneities.

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Year:  2018        PMID: 29582994     DOI: 10.1021/acs.analchem.7b04874

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  1 in total

1.  The nanotopography of SiO2 particles impacts the selectivity and 3D fold of bound allergens.

Authors:  Robert Mills-Goodlet; Litty Johnson; Isabel J Hoppe; Christof Regl; Mark Geppert; Milena Schenck; Sara Huber; Michael Hauser; Fátima Ferreira; Nicola Hüsing; Christian G Huber; Hans Brandstetter; Albert Duschl; Martin Himly
Journal:  Nanoscale       Date:  2021-12-16       Impact factor: 7.790

  1 in total

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