arXiv subjects

Frank Sobott

Publications and source records attributed to Frank Sobott.

3 recordsLinked to original sources

arXiv2020

Towards Increased Reliability, Transparency and Accessibility in Crosslinking Mass Spectrometry

Crosslinking mass spectrometry (Crosslinking MS) has substantially matured as a method over the last two decades through parallel development in multiple labs, demonstrating its applicability for protein structure determination, conformation analysis and mapping protein interactions in complex mixtures. Crosslinking MS has become a much-appreciated and routinely applied tool especially in structural biology. Therefore, it is timely that the community commits to the development of methodological and reporting standards. This white paper builds on an open process comprising a number of events at community conferences since 2015 and identifies aspects of Crosslinking MS for which guidelines should be developed as part of a Crosslinking MS standards initiative.

q-bio.OT↗

arXiv2017

Assigning peaks and modeling ETD in top-down mass spectrometry

Among many techniques of modern mass spectrometry, the top down methods are becoming continuously more popular in the overall strive to describe the proteome. These techniques are based on fragmentation of ions inside mass spectrometers instead of being proteolytically digested. In some of these techniques, the fragmentation is induced by electron transfer. It can trigger several concurring reactions: electron transfer dissociation, electron transfer without dissociation, and proton transfer reaction. The evaluation of the extent of these reactions is important for the proper understanding of the functioning of the instrument and, what is even more important, to know if it can be used to reveal important structural information. We present a workflow for assigning peaks and interpreting the results of electron transfer driven reactions. We also present software written in Python and available under GNU v3 license.

stat.AP↗

arXiv2017

Proton Dynamics in Protein Mass Spectrometry

Native electrospray ionization/ion mobility-mass spectrometry (ESI/IM-MS) allows an accurate determination of low-resolution structural features of proteins. Yet, the presence of proton dynamics, observed already by us for DNA in the gas phase, and its impact on protein structural determinants, have not been investigated so far. Here, we address this issue by a multi-step simulation strategy on a pharmacologically relevant peptide, the N-terminal residues of amyloid-beta peptide (Abeta(1-16)). Our calculations reproduce the experimental maximum charge state from ESI-MS and are also in fair agreement with collision cross section (CCS) data measured here by ESI/IM-MS. Although the main structural features are preserved, subtle conformational changes do take place in the first ~0.1 ms of dynamics. In addition, intramolecular proton dynamics processes occur on the ps-timescale in the gas phase as emerging from quantum mechanics/molecular mechanics (QM/MM) simulations at the B3LYP level of theory. We conclude that proton transfer phenomena do occur frequently during fly time in ESI-MS experiments (typically on the ms timescale). However, the structural changes associated with the process do not significantly affect the structural determinants.

physics.chem-ph↗