Evidence map›Paper›PMID 40620802›Full record

ArticleBio-protocol2025

Protein Structural Characterization Using Electron Transfer Dissociation and Hydrogen Exchange-Mass Spectrometry.

Rupam Bhattacharjee, Jayant B Udgaonkar

Abstract read
In one paragraph

Article in Bio-protocol, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Rupam BhattacharjeeNational Centre for Biological Sciences, Tata Institute of Fundamental Research, Bengaluru, India.
Jayant B UdgaonkarDeptartment of Biology, Indian Institute of Science Education and Research Pune, Pune, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intermediate states are often populated during the folding and unfolding reactions of a protein, and their detection is very challenging as they form transiently. Structural characterization of these short-lived intermediate species is difficult as it requires high-resolution methodologies. Hydrogen exchange-mass spectrometry (HX-MS) can identify and yield direct structural information on folding and unfolding intermediates, as well as information about the cooperativity of the folding or unfolding processes. The mass distributions of intact protein molecules are obtained first to determine their exchange pattern. Then, segment-specific structural information is obtained by analyzing the fragments of the protein. Enzymatic digestion is widely used with HX to determine the sequence-specific structural changes that occur to the protein during folding or unfolding. However, if a protein is an inhibitor of the protease, then alternative methodologies are required. Using electron transfer dissociation (ETD), it is possible to fragment the protein inside a mass spectrometer, and segment-specific structural changes occurring during the folding and unfolding process can be determined. In the case of HX-ETD-MS, protein molecules are first allowed to undergo HX, followed by their fragmentation. Deuterium retention in each fragment is measured. Very little, if any, scrambling of deuterium across fragments occurs during ETD-enabled fragmentation; hence, there is little scope for misinterpretation of the HX data. Key features • Analysis of intact protein data allows the identification of the intermediate states even in native and native-like conditions. • Precursor mass is determined from the intact protein analysis. • Fragments undergoing cooperative and non-cooperative transitions during protein unfolding can be distinguished from each other using HX-ETD-MS. • Analysis of the protein fragments that are obtained using ETD also enables the determination of the sequence of structural changes occurring in the protein. • HX-ETD-MS can provide structural insights into transiently formed intermediate states.

Indexed as

Back-exchangeCooperativeDeuteriumGlobal fittingIntermediateKineticsNon-cooperative

Identifiers

PMID40620802
PMCPMC12222632

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