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Exploiting small angle X-ray and neutron scattering (SAXS/SANS) on the same sample volume at the same time provides complementary nanoscale structural information at two different contrast situations. Compared with an independent experimental approach, the truly combined SAXS/SANS experimental approach ensures the exactness of the probed samples particularly for in-situ studies. Here, we introduce an advanced portable SAXS system that is dimensionally suitable for installation at D22 zone of ILL. The SAXS apparatus is based on a RIGAKU copper/molybdenum switchable microfocus rotating anode X-ray generator and a DECTRIS detector with a changeable sample-to-detector distance of up to 1.6 m in a vacuum chamber. A science case has been presented to demonstrate the uniqueness of the newly established method at ILL. Temporal structural rearrangements of both, organic stabilizing agents and organically capped gold colloidal particles during gold nanoparticle growth are simultaneously probed, enabling immediate correlated structural information. The newly established nano-analytical method at ILL will open the way for real time investigations of a wide range of innovative nanomaterials and will enable comprehensive in-situ studies on biological systems. A potential development of a fully-automated SAXS/SANS system with a common control environment and additional sample environments, permitting a continual and efficient operation of the system at the hands of ILL users, has also been introduced., Comment: 22 pages, 9+2 figures

Monitoring the kinetics and conformational dynamics of single enzymes is crucial in order to better understand their biological functions as these motions and structural dynamics are usually unsynchronized among the molecules. Detecting the enzyme-reactant interactions and associated conformational changes of the enzyme on a single molecule basis, however, remain as a challenge with established optical techniques due to the commonly required labeling of the reactants or the enzyme itself. The labeling process is usually non-trivial and the labels themselves might skew the physical properties of the enzyme. Here we demonstrate an optical, label-free method capable of observing enzymatic interactions and the associated conformational changes on the single molecule level. We monitor polymerase/DNA interactions via the strong near-field enhancement provided by plasmonic nanorods resonantly coupled to whispering gallery modes in microcavities. Specifically, we employ two different recognition schemes: one in which the kinetics of polymerase/DNA interactions are probed in the vicinity of DNA-functionalized nanorods, and the other in which these interactions are probed via the magnitude of conformational changes in the polymerase molecules immobilized on nanorods. In both approaches we find that low and high polymerase activities can be clearly discerned via their characteristic signal amplitude and signal length distributions. Furthermore, the thermodynamic study of the monitored interactions suggests the occurrence of DNA polymerization. This work constitutes a proof-of-concept study of enzymatic activities via plasmonically enhanced microcavities and establishes an alternative and label-free method capable of investigating structural changes in single molecules.