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Vollmer, F.

Publications and source records attributed to Vollmer, F..

2 recordsLinked to original sources

Thermo-optoplasmonic single-molecule sensing on optical microcavities

Whispering-gallery-mode (WGM) resonators are powerful instruments for single-molecule sensing in biological and biochemical investigations. WGM sensors leveraged by plasmonic nanostructures, known as optoplasmonic sensors, provide unprecedented sensitivity down to single atomic ions. In this article, we describe that the response of optoplasmonic sensors upon the attachment of single protein molecules strongly depends on the intensity of WGM. At low intensity, protein binding causes red shifts of WGM resonance wavelengths, known as the reactive sensing mechanism. By contrast, blue shifts are obtained at high intensities, which we explain as thermo-optoplasmonic (TOP) sensing, where molecules transform absorbed WGM radiation into heat. To support our conclusions, we experimentally investigated seven molecules and complexes; we observed blue shifts for dye molecules, amino acids and anomalous absorption of enzymes in the near-infrared spectral region. As an example of application, we propose a physical model of TOP sensing that can be used for the development of single-molecule absorption spectrometers. Significance StatementA notable contribution to the optical detection of single molecules has been brought about by using optical microcavities, specifically whispering-gallery-mode resonators that combine optical and plasmon resonances for the most sensitive single-molecule and ion detection. Adding absorption measurements to a single-molecule technique that operates in an aqueous solution would provide powerful new detection capabilities for sensing the properties of single molecules. We demonstrate here, for the first time, the detection of absorption cross-sections of protein molecules on optoplasmonic microcavities and validate the technique with seven different molecules and complexes. A proof-of-concept for single-molecule optoplasmonic absorption spectrometers is presented, based on a thermo-optoplasmonic sensing mechanism.

biophysics↗

Allosteric regulation of glycogen phosphorylase solution phase structural dynamics at high spatial resolution

Glycogen phosphorylase (GlyP) was the first allosteric enzyme to be described. Yet, the precise dynamic changes in solution phase structure and stability that underpin functional regulation have remained elusive. We have developed a new fully-automated and highly flexible implementation of hydrogen/deuterium-exchange mass spectrometry, operating in the millisecond regime. This enabled measurements of the solution phase local structural dynamics involved in allosteric regulation of GlyP. Here, we quantify GlyP structural dynamics in solution, describing correlated changes in structure in the activated (pSer14) and inhibited (glucose-6-phosphate bound) forms of the enzyme. The sensitivity of these measurements discerned that the 250s loop is natively disordered in the apo T-state, adopting a more ordered conformation in the active state. The quantitative change in stability of the 280s loop is identified, providing the first direct evidence of the entropic switch that sterically regulates substrate access to the active site.\n\nSignificance StatementWe have developed a new fully-automated and highly flexible implementation of hydrogen/deuterium-exchange mass spectrometry, operating in the millisecond regime. Measurements of glycogen phosphorylase quantify the solution phase stability of local structure at near-amino acid structural resolution and with no appreciable lower limit of stability. This uncovered the highly-resolved local alterations in stability which provides direct evidence of the entropic mechanism by which access to the active site is gated by the 280s loop.\n\nFootnotesAuthor contributions: M.K., V.S., S.S., N.L., F.V., N.B., L.C. and J.J.P. designed research; M.K., V.S., S.S., L.C. and J.J.P. performed research; M.K., V.S., S.S., L.C. and J.J.P. analyzed data; and M.K. and J.J.P. wrote the manuscript.

biophysics↗