Evidence map›Paper›PMID 38945838›Full record

ArticleChemphyschem : a European journal of chemical physics and physical chemistry2024

Scanning Probe Microscopy Characterization of Biomolecules enabled by Mass-Selective, Soft-landing Electrospray Ion Beam Deposition.

Johannes Seibel, Kelvin Anggara, Martina Delbianco, Stephan Rauschenbach

Abstract read
In one paragraph

Article in Chemphyschem : a European journal of chemical physics and physical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Self-Assembly, Rearrangement, and Disassembly of {CrAngewandte Chemie (International ed. in English) · 2025
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Johannes SeibelInstitute of Physical Chemistry, Karlsruhe Institute of Technology, Fritz-Haber Weg 2, D-76131, Karlsruhe, Germany.ORCID 0000-0002-0286-0202
Kelvin AnggaraNanoscale Science Department, Max Planck Institute for Solid State Research, Heisenbergstr. 1, D-70569, Stuttgart, Germany.ORCID 0000-0001-8598-8035
Martina DelbiancoDepartment of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, D-14476, Potsdam, Germany.ORCID 0000-0002-4580-9597
Stephan RauschenbachDepartment of Chemsitry, University of Oxford, OX13TA, Oxford, UK.ORCID 0000-0001-9382-1948

Funding

European Research Council 101075996European Research Council (ERC)GLYCOFOLDGlycoXHorizon Europe 101075357Max Planck Society, the German Federal Ministry of Education and Research (BMBF 13XP5114M. Kappes and KIT 101075996UKRI BB/V019694/1UKRI BB/W017024/1UKRI EP/V051474/1)
6 · The paper itself

Abstract

Scanning probe microscopy (SPM), in particular at low temperature (LT) under ultra-high vacuum (UHV) conditions, offers the possibility of real-space imaging with resolution reaching the atomic level. However, its potential for the analysis of complex biological molecules has been hampered by requirements imposed by sample preparation. Transferring molecules onto surfaces in UHV is typically accomplished by thermal sublimation in vacuum. This approach however is limited by the thermal stability of the molecules, i. e. not possible for biological molecules with low vapour pressure. Bypassing this limitation, electrospray ionisation offers an alternative method to transfer molecules from solution to the gas-phase as intact molecular ions. In soft-landing electrospray ion beam deposition (ESIBD), these molecular ions are subsequently mass-selected and gently landed on surfaces which permits large and thermally fragile molecules to be analyzed by LT-UHV SPM. In this concept, we discuss how ESIBD+SPM prepares samples of complex biological molecules at a surface, offering controls of the molecular structural integrity, three-dimensional shape, and purity. These achievements unlock the analytical potential of SPM which is showcased by imaging proteins, peptides, DNA, glycans, and conjugates of these molecules, revealing details of their connectivity, conformation, and interaction that could not be accessed by any other technique.

Indexed as

Microscopy, Scanning ProbeDNAIonsProteinsSpectrometry, Mass, Electrospray IonizationSurface PropertiesDNAIonsProteinsElectrospray ionizationGlycansMass spectrometrySaccharidesScanning probe microscopy

Identifiers

PMID38945838
PMCPMC7617705

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.