» Articles » PMID: 37436406

ProSight Native: Defining Protein Complex Composition from Native Top-Down Mass Spectrometry Data

Overview
Journal J Proteome Res
Specialty Biochemistry
Date 2023 Jul 12
PMID 37436406
Authors
Affiliations
Soon will be listed here.
Abstract

Native mass spectrometry has recently moved alongside traditional structural biology techniques in its ability to provide clear insights into the composition of protein complexes. However, to date, limited software tools are available for the comprehensive analysis of native mass spectrometry data on protein complexes, particularly for experiments aimed at elucidating the composition of an intact protein complex. Here, we introduce ProSight Native as a start-to-finish informatics platform for analyzing native protein and protein complex data. Combining mass determination via spectral deconvolution with a top-down database search and stoichiometry calculations, ProSight Native can determine the complete composition of protein complexes. To demonstrate its features, we used ProSight Native to successfully determine the composition of the homotetrameric membrane complex Aquaporin Z. We also revisited previously published spectra and were able to decipher the composition of a heterodimer complex bound with two noncovalently associated ligands. In addition to determining complex composition, we developed new tools in the software for validating native mass spectrometry fragment ions and mapping top-down fragmentation data onto three-dimensional protein structures. Taken together, ProSight Native will reduce the informatics burden on the growing field of native mass spectrometry, enabling the technology to further its reach.

Citing Articles

Defining proteoform-specific interactions for drug targeting in a native cell signalling environment.

Lutomski C, Bennett J, El-Baba T, Wu D, Hinkle J, Burnap S Nat Chem. 2025; 17(2):204-214.

PMID: 39806141 PMC: 11794133. DOI: 10.1038/s41557-024-01711-w.


Structural Analysis of the 20S Proteasome Using Native Mass Spectrometry and Ultraviolet Photodissociation.

Walker J, Gautam A, Matouschek A, Brodbelt J J Proteome Res. 2024; 23(12):5438-5448.

PMID: 39475212 PMC: 11660092. DOI: 10.1021/acs.jproteome.4c00568.


Improving Top-Down Sequence Coverage with Targeted Fragment Matching.

Robey M, Durbin K J Am Soc Mass Spectrom. 2024; 35(12):3296-3300.

PMID: 39437430 PMC: 11623164. DOI: 10.1021/jasms.4c00161.


Towards a universal method for middle-down analysis of antibodies via proton transfer charge reduction-Orbitrap mass spectrometry.

Oates R, Lieu L, Kline J, Mullen C, Srzentic K, Huguet R Anal Bioanal Chem. 2024; 416(28):6463-6472.

PMID: 39283368 PMC: 11837950. DOI: 10.1007/s00216-024-05534-z.


Top-down mass spectrometry analysis of capsid proteins of recombinant adeno-associated virus using multiple ion activations and proton transfer charge reduction.

Kline J, Huang J, Lieu L, Srzentic K, Bergen D, Mullen C Proteomics. 2024; :e2400223.

PMID: 39233542 PMC: 11880350. DOI: 10.1002/pmic.202400223.


References
1.
Rose A, Hildebrand P . NGL Viewer: a web application for molecular visualization. Nucleic Acids Res. 2015; 43(W1):W576-9. PMC: 4489237. DOI: 10.1093/nar/gkv402. View

2.
Jooss K, McGee J, Kelleher N . Native Mass Spectrometry at the Convergence of Structural Biology and Compositional Proteomics. Acc Chem Res. 2022; 55(14):1928-1937. PMC: 9296611. DOI: 10.1021/acs.accounts.2c00216. View

3.
Moehring F, Waas M, Keppel T, Rathore D, Cowie A, Stucky C . Quantitative Top-Down Mass Spectrometry Identifies Proteoforms Differentially Released during Mechanical Stimulation of Mouse Skin. J Proteome Res. 2018; 17(8):2635-2648. PMC: 6195672. DOI: 10.1021/acs.jproteome.8b00109. View

4.
Jumper J, Evans R, Pritzel A, Green T, Figurnov M, Ronneberger O . Highly accurate protein structure prediction with AlphaFold. Nature. 2021; 596(7873):583-589. PMC: 8371605. DOI: 10.1038/s41586-021-03819-2. View

5.
Bern M, Caval T, Kil Y, Tang W, Becker C, Carlson E . Parsimonious Charge Deconvolution for Native Mass Spectrometry. J Proteome Res. 2018; 17(3):1216-1226. PMC: 5838638. DOI: 10.1021/acs.jproteome.7b00839. View