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The lexicon of noncovalent molecular interactions has become rather extensive.
Experimentation in the use of supercomputers to model molecular interactions has been going on for more than a decade, but the field is still largely in its infancy.
Identification of core clock components and their associated molecular interactions has established the basic network architecture of plant clocks, which consists of multiple interlocked feedback loops.
Assumptions that oversimplify are gradually being eliminated as access to computational hardware becomes less restrictive, and a deeper appreciation of the dynamics of molecular interactions has been compelled by the experimental data.
To date, the zebrafish has been mainly used to identify molecular targets of EDC action and to determine effect thresholds, while the potential of this model species to study immediate and delayed physiological consequences of molecular interactions has been instrumentalized only partly.
Fluorescence labeling and optical detection of molecular interactions has become an indispensable tool in biology.
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Molecular interactions have been examined by calculating and discussing solvation functions and Kirkwood Buff (KB) integrals.
The HAP polymer interfacial molecular interactions have significant role on the mechanical response of composite systems.
Furthermore, the 3D supramolecular networks, formed through plentiful H-bonds and weak molecular interactions, have been analyzed.
Both rational, design-based approaches as well as hybrid approaches where high throughput screening has been coupled to an understanding of critical molecular interactions have been productive in advancing understanding of physiology and potential therapeutics in this field.
Numerous cellular and molecular interactions have been identified by which immune cells can intervene in the metastatic cascade, leading to the development of several in vivo and in vitro model systems that can recapitulate these processes.
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