Human C-reactive protein (CRP) is a classical, acute phase serum protein synthesized by the liver in response to infection, inflammation, or trauma. CRP binds to microbial antigens and damaged cells, opsonizes particles for phagocytosis and regulates the inflammatory response by the induction of cytokine synthesis. These activities of CRP depend on its ability to activate complement and to bind to Fc␥ receptors (Fc␥R). The goal of this study was to elucidate amino acid residues important for the interaction of CRP with human Fc␥RI (CD64) and Fc␥RIIa (CD32). Several mutations of the CRP structure were studied based on the published crystal structure of CRP.

Escape swimming is a crucial behavior by which undulatory swimmers evade potential threats. The hydrodynamics of escape swimming have not been well studied, particularly for anguilliform swimmers, such as the sea lamprey Petromyzon marinus. For this study, we compared the kinematics and hydrodynamics of larval sea lampreys with those of lampreys accelerating from rest during escape swimming. We used experimentally derived velocity fields to calculate pressure fields and distributions of thrust and drag along the body. Lampreys initiated acceleration from rest with the formation of a highamplitude body bend at approximately one-quarter body length posterior to the head. This deep body bend produced two highpressure regions from which the majority of thrust for acceleration was derived. In contrast, steady swimming was characterized by shallower body bends and negative-pressure-derived thrust, which was strongest near the tail. The distinct mechanisms used for steady swimming and acceleration from rest may reflect the differing demands of the two behaviors. High-pressure-based mechanisms, such as the one used for acceleration from rest, could also be important for low-speed maneuvering during which drag-based turning mechanisms are less effective. The design of swimming robots may benefit from the incorporation of such insights from unsteady swimming.

Several species of large, centric diatoms exhibit an unsteady sinking behaviour characterized by order-of-magnitude oscillations in sinking speed that occur over seconds. We show that under nutrient-depleted conditions, Coscinodiscus wailesii exhibits significantly stronger unsteady sinking behaviour in the light than in the dark. Results suggest that regulating unsteady sinking in response to irradiance as well as nutrient conditions may help C. wailesii balance its requirements for light and nutrients, which are often spatially separated.

A diatom's sinking speed affects its depth in the water column, which determines its access to light and nutrients. Some large, centric diatom species perform an unsteady sinking behavior in which a cell's sinking speed oscillates over more than an order of magnitude on time scales of seconds. Diatoms are known to decrease mean sinking speeds and the magnitude of unsteady sinking following exposure to nutrient replete conditions over hours to days. Here we show that on shorter time scales of minutes to hours, nutrient deprived Coscinodiscus wailesii cells increase the mean and unsteadiness of their sinking when exposed to increased nutrient concentrations. Cultures exposed to nitrate or silicate‐depleted media followed by a spike of the missing nutrient showed a sinking speed increase within the first 2 h that declined over the next 22 h. Phosphate deprived cultures did not respond similarly to a phosphate spike. In an experiment with an artificial nutricline in which cells encountered a sharp increase in nutrient concentrations over a distance of 10 cm, mean sinking speeds increased eight fold, and sinking unsteadiness increased significantly; these sinking speed changes occurred over 33 min. The contrasting short and long‐term sinking behavior responses seen in this study demonstrates the importance of examining sinking behavior over multiple time scales. Initial fast and unsteady sinking upon encountering increasing nutrient concentrations may help diatoms take advantage of patchy nutrient distributions. Longer term, slow and steady sinking may be beneficial for maximizing light exposure and minimizing energy costs from unsteady sinking.