Eller, J. | Search bioRxiv

bioRxiv2022

Improved Yield for the Enzymatic Synthesis of Radiolabeled Nicotinamide Adenine Dinucleotide

Labeled {beta}-nicotinamide adenine dinucleotide (NAD) analogs have been critical for uncovering new biochemical connections and quantitating enzymatic activity. They function as tracers for enzymology, flux analyses, and in situ measurements. Nevertheless, there is limited availability of specific types of analogs, especially radiolabeled NAD analogs. Here, we describe an improved enzymatic synthesis reaction for 32P-NAD+ with a yield of 98% {+/-} 1%, using lowered concentrations of reactants and standard equipment. This represents the highest reported yield for the enzymatic synthesis of NAD+ to date. With the high yield we were able to directly use the reaction product to generate derivatives, such as 32P-NADP. The high-yield enzymatic synthesis is versatile for a broad variety of labels and NAD derivatives. Its advantages include lowered concentrations of reactants, providing sufficient amounts of product for downstream applications, and minimizing intermediate purification steps.

biochemistry↗

bioRxiv2021

Long-Range Electrostatic Interactions Significantly Modulate the Affinity of Dynein for Microtubules

The dynein family of microtubule minus-end directed motor proteins drives diverse functions in eukaryotic cells, including cell division, intracellular transport, and flagellar beating. Motor protein processivity, which characterizes how far a motor walks before detaching from its filament, depends on the interaction between its microtubule-binding domain (MTBD) and the microtubule. Dyneins MTBD switches between high- and low-binding affinity states as it steps. Significant structural and functional data show that specific salt bridges within the MTBD and between the MTBD and the microtubule govern these affinity state shifts. However, recent computational work suggests that non-specific, long-range electrostatic interactions between the MTBD and the microtubule may also play a significant role in the processivity of dynein. To investigate this hypothesis, we mutated negatively charged amino acids remote from the dynein MTBD-microtubule-binding interface to neutral residues and measured the binding affinity using microscale thermophoresis and optical tweezers. We found a significant increase in the binding affinity of the mutated MTBDs for microtubules. Furthermore, we found that charge screening by free ions in solution differentially affected the binding and unbinding rates of MTBDs to microtubules. Together, these results demonstrate a significant role for long-range electrostatic interactions in regulating dynein-microtubule affinity. Moreover, these results provide insight into the principles that potentially underlie the biophysical differences between molecular motors with various processivities and protein-protein interactions more generally. Statement of SignificanceThe dynein family of motor proteins drives the motility of multiple cellular functions by walking toward the minus end of microtubules. The biophysical mechanisms of dynein rely on its ability to change affinity for the microtubule as it steps. Specific short-range electrostatic interactions acting at the microtubule-binding domain (MTBD)-microtubule interface are known to govern binding affinity. This study shows that non-specific longer-range electrostatic interactions due to charged amino acids remote from the binding interface also contribute significantly to the binding affinity mechanisms. Our results suggest that subtle differences in the electrostatic charge distribution within the MTBD significantly affect the molecular biophysical motility mechanisms in the dynein family of motors.

biophysics↗