Scattering microscopy
A scattering microscopy arrangement uses a microscope to image an object comprising a surface. A light source emits illuminating light and a light detector detects light elastically scattered from the object. An electric potential is applied to the surface that affects the electrochemical properties of the object while imaging. The electric potential provides a contrast mechanism that improves the imaging and allows for characterisation of the object and/or the surrounding environment.
1 . A method of monitoring and controlling the binding rate of a particle, the method comprising the steps of;
imaging an object having a surface and at least one particle with a scattering microscope including a light source arranged to emit illuminating light and a light detector,
the microscope further arranged to illuminate the object with the illuminating light and to detect light elastically scattered from the object with the light detector; and
applying an electrical potential to the surface of the object to change the electrochemical state of the surface; wherein the change of the electrochemical state permits monitoring and controlling of the rate of binding of the particle to the surface, wherein the object is being selected not to have a plasmon resonance frequency at the wavelengths of the illuminating light and at the applied electrical potential.
2 . The method according to claim 1 , wherein an electric double layer forms at the surface and the electrical potential to the surface affects the electrochemical properties of the electric double layer.
3 . The method according to claim 1 , wherein the surface is a surface of a conductive material and the step of applying an electrical potential to the surface comprises applying the potential to the conductive material.
4 . The method according to claim 1 , further comprising the step of selectively rejecting or attracting a particle to the surface by applying electrical potential to the surface.
5 . The method according to claim 1 , wherein the particle is a dielectric particle.
6 . The method according to claim 1 , wherein the particle is a protein or an aggregate of proteins, a polypeptide, a glycopolypeptide or glycoprotein, a lipopolypeptide or lipoprotein or any aggregate thereof, a lipid, a proteoglycan, or a sugar polymer.
7 . The method according to claim 1 , wherein the particle may be a nucleic acid molecule, such as an RNA (ribonucleic acid) or DNA (deoxyribonucleic acid), or an artificial nucleic acid molecule, or any aggregate thereof.
8 . The method according to claim 1 , wherein the particle has a mass of 10 kDa or more.
9 . The method according to claim 1 , wherein the particle has a mass of 5000 kDa or less.
10 . The method according to claim 1 , further comprising the step of monitoring interactions between the object and constituents in the surrounding environment, wherein the constituents are molecules or ions.
11 . The method according to claim 10 , further comprising the step of adjusting the binding/unbinding rate of molecules in solution to the surface of the object.
12 . The method according to claim 1 , comprising the step of applying a plurality of different electrical potential to the surface.
13 . The method according to claim 12 , further comprising the step of comparing measurements taken at different electrical potentials.
14 . The method according to claim 1 , wherein the object is a single nanoscopic object.
15 . The method according to claim 14 , comprising the step of monitoring the properties and electrochemical state of the single nanoscopic object.