Method, apparatus and system for characterizing transient interactions between biomolecules

Patent metadata

Field	Value
Publication number	US-2024183778-A1
Application number	US-202218553833-A
Country	US
Kind code	A1
Filing date	Apr 7, 2022
Priority date	Apr 8, 2021
Publication date	Jun 6, 2024
Grant date	—

Abstract

The invention relates to a method, an apparatus and system for characterizing transient interactions between biomoleules. wherein the method comprises following steps: providing a plurality of plasmonic nanoparticles which are configured to allow first biomolecules to adhere thereto: providing a mixture comprising the nanoparticles. first biomolecules and second biomolecules to allow the first biomolecules to adhere to the nanoparticles and to allow the second biomolecules to. in particular transiently, interact with the first biomolecules adherent to the nanoparticles: irradiating the mixture with first electromagnetic radiation, in particular broadband electromagnetic radiation: detecting second electromagnetic radiation, which is scattered by the mixture while irradiating the mixture with the first electromagnetic radiation, in a time-resolved and spectrally-resolved manner so as to obtain intensity signals representing changes in the spectrum of the detected second electromagnetic radiation: and determining at least one interaction parameter characterizing transient interactions of the second biomolecules with the first biomolecules based on the intensity signals.

First claim

1 . A method for characterizing transient interactions between biomolecules comprising following steps:
providing a plurality of plasmonic nanoparticles which are configured to allow first biomolecules to adhere thereto, providing a mixture comprising the nanoparticles, first biomolecules and second to allow the first biomolecules to adhere to the nanoparticles and to allow the second biomolecules to, in particular transiently, interact with the first biomolecules adherent to the nanoparticles, irradiating the mixture with first electromagnetic radiation, in particular broadband electromagnetic radiation, detecting second electromagnetic radiation, which is scattered by the mixture while irradiating the mixture with the first electromagnetic radiation, in a time-resolved and spectrally-resolved manner so as to obtain intensity signals representing changes in the spectrum of the detected second electromagnetic radiation, and determining at least one interaction parameter characterizing transient interactions of the second biomolecules with the first biomolecules based on the intensity signals.

2 . The method according to claim 1 , wherein the step of detecting the second electromagnetic radiation comprises
splitting the second electromagnetic radiation into a first partial beam and a second partial beam, providing one or more different path length differences between the first partial beam and the second partial beam, superimposing the first partial beam and the second partial beam for each of the path length differences so as to obtain a first interference beam and a second interference beam for each of the path length differences, and separately detecting the first interference beam and the second interference beam by means of two separate detectors at different times and for each of the path length differences so as to obtain two series of intensity signals representing intensities of the first interference beam and second interference beam, respectively, at the different times and for the different path length differences.

3 . The method according to claim 1 , wherein the step of detecting the second electromagnetic radiation comprises
applying the second electromagnetic radiation to at least one spectral splitting element, in particular a dichroic optical element, so as to obtain at least one first partial beam of electromagnetic radiation having a first spectrum and at least one second partial beam of electromagnetic radiation having a second spectrum which is different from the first spectrum, and separately detecting the first partial beam and the second partial beam by means of two separate detectors at different times so as to obtain two series of intensity signals representing intensities of the first partial beam and second partial beam, respectively, at the different times and for the first and second spectrum.

4 . The method according to claim 2 further comprising determining at least one time auto-correlation function (intensity-time auto-correlation function) characterizing a time auto-correlation of a combination of the two series of intensity signals, wherein at least one diffusion parameter characterizing a diffusion of the nanoparticles in the mixture is determined based on the at least one time auto-correlation function.

5 . The method according to claim 2 further comprising determining at least one time cross-correlation function (intensity-time cross-correlation function) characterizing a time cross-correlation between the two series of intensity signals, wherein the at least one interaction parameter is determined based on the at least one time cross-correlation function and optionally also on the at least one time autocorrelation function.

6 . The method according to claim 4 , wherein the at least one time auto-correlation function and/or the at least one time cross-correlation function is determined for the different path length differences between the first partial beam and the second partial beam or for the first and second spectrum, respectively.

7 . The method according to claim 4 , wherein the time auto-correlation function (intensity-time auto-correlation function) is used to correct the time cross-correlation function (intensity-time cross-correlation function) to remove effects of nanoparticle diffusion on the time cross-correlation function.

8 . The method according to claim 7 , wherein the at least one interaction parameter is determined based, in particular based only, on the corrected intensity cross-correlation function.

9 . The method according to claim 5 further comprising Fourier transforming the time cross-correlation functions, which are determined for the different path length differences, with respect to the dimension of the path length differences so as to obtain spectral correlation functions (spectral-time correlation function) at different times and for different wavelength changes, wherein the at least one interaction parameter is determined based on the spectral correlation functions.

10 . The method according to claim 9 further comprising determining a temporal behavior of the spectral correlation functions, wherein the at least one interaction parameter is determined based on the temporal behavior of the spectral correlation functions and/or intensity correlation functions.

11 . The method according to claim 1 , wherein determining the at least one interaction parameter includes determining at least one parameter characterizing reversible interactions between the first and second biomolecules.

12 . The method according to claim 1 , wherein determining the at least one interaction parameter includes determining at least one of the following:
a first transition rate characterizing a time rate at which transitions occur between an unbound state, in which the second biomolecules are not bound to and/or do not interact with first biomolecules, to a bound state, in which the second biomolecules are bound to and/or interact with the first biomolecules, and/or a second transition rate characterizing a time rate at which transitions occur between a bound state, in which the second biomolecules are bound to and/or interact with the first biomolecules, to an unbound state, in which the second biomolecules are not bound to and/or do not interact with the first biomolecules, and/or a dissociation constant characterizing a tendency of the first and second biomolecules to reversibly dissociate between a bound state, in which the second biomolecules are bound to and/or interact with the first biomolecules, and an unbound state, in which the second biomolecules are not bound to and/or do not interact with the first biomolecules.

13 . The method according to claim 1 , wherein the mixture comprising the nanoparticles, first biomolecules and second biomolecules is a solution and/or dispersion, wherein the nanoparticles, first biomolecules and second biomolecules are dissolved in a solvent or dispersed in a dispersion agent, respectively.

14 . An apparatus for characterizing transient interactions between biomolecules comprising:
a receptacle configured to receive a mixture comprising first biomolecules, second biomolecules and a plurality of plasmonic nanoparticles which are configured to allow at least a part of the first biomolecules to adhere thereto, wherein at least a part of the second biomolecules are allowed to, in particular transiently, interact with first biomolecules adherent to the nanoparticles, an irradiation unit configured to irradiate the mixture with first electromagnetic radiation, in particular broadband electromagnetic radiation, a detection unit configured to det

Assignees

• Helmholtz Zentrum Muenchen Deutsches Forschungszentrum Gesundheit & Umwelt Gmbh

Inventors

• Cui Jian
• Ridderbeek Korneel

Classifications

• G01N21/4738 Primary

  Diffuse reflection (precedence is given to G01N21/55 - G01N21/57 if specular component is taken into consideration), e.g. also for testing fluids, fibrous materials · CPC title

• G01N21/554 Primary

  detecting the surface plasmon resonance of nanostructured metals, e.g. localised surface plasmon resonance · CPC title

• G01N21/272

  for following a reaction, e.g. for determining photometrically a reaction rate (photometric cinetic analysis) · CPC title