Molecular motor

uses protein domain dynamics on nanoscales to walk along a microtubule. Some examples of biologically important molecular motors: • Cytoskeletal motors • Myosins are responsible for muscle contraction, intracellular cargo transport, and producing cellular tension. • Kinesin moves cargo inside cells away from the nucleus along microtubules, in anterograde transport. • Dynein produces the axonemal beating of cilia and flagella and also transports cargo along microtubules towards the cell nucleus, in retrograde transport. • Polymerisation motors • Actin polymerization generates forces and can be used for propulsion. ATP is used. • Microtubule polymerization using GTP. • Dynamin is responsible for the separation of clathrin buds from the plasma membrane. GTP is used. • Rotary motors: • FoF1-ATP synthase family of proteins convert the chemical energy in ATP to the electrochemical potential energy of a proton gradient across a membrane or the other way around. The catalysis of the chemical reaction and the movement of protons are coupled to each other via the mechanical rotation of parts of the complex. This is involved in ATP synthesis in the mitochondria and chloroplasts as well as in pumping of protons across the vacuolar membrane. • The bacterial flagellum responsible for the swimming and tumbling of E. coli and other bacteria acts as a rigid propeller that is powered by a rotary motor. This motor is driven by the flow of protons across a membrane, possibly using a similar mechanism to that found in the Fo motor in ATP synthase. composed of three molecules in a nanopore (outer diameter 6.7 nm) at 250 K. • Nucleic acid motors: • RNA polymerase transcribes RNA from a DNA template. • DNA polymerase turns single-stranded DNA into double-stranded DNA. • Helicases separate double strands of nucleic acids prior to transcription or replication. ATP is used. • Topoisomerases reduce supercoiling of DNA in the cell. ATP is used. • RSC and SWI/SNF complexes remodel chromatin in eukaryotic cells. ATP is used. • SMC proteins responsible for chromosome condensation in eukaryotic cells. • Viral DNA packaging motors inject viral genomic DNA into capsids as part of their replication cycle, packing it very tightly. Several models have been put forward to explain how the protein generates the force required to drive the DNA into the capsid. An alternative proposal is that, in contrast with all other biological motors, the force is not generated directly by the protein, but by the DNA itself. In this model, ATP hydrolysis is used to drive protein conformational changes that alternatively dehydrate and rehydrate the DNA, cyclically driving it from B-DNA to A-DNA and back again. A-DNA is 23% shorter than B-DNA, and the DNA shrink/expand cycle is coupled to a protein-DNA grip/release cycle to generate the forward motion that propels DNA into the capsid. • Enzymatic motors: The enzymes below have been shown to diffuse faster in the presence of their catalytic substrates, known as enhanced diffusion. They also have been shown to move directionally in a gradient of their substrates, known as chemotaxis. Their mechanisms of diffusion and chemotaxis are still debated. Possible mechanisms include solutal buoyancy, phoresis or conformational changes leading to change in effective diffusivity and kinetic asymmetry. • Catalase • Urease • Aldolase • Hexokinase • Phosphoglucose isomerase • Phosphofructokinase • Glucose oxidase A recent study has also shown that certain enzymes, such as Hexokinase and Glucose Oxidase, are aggregating or fragmenting during catalysis. This changes their hydrodynamic size that can affect enhanced diffusion measurements. • Synthetic molecular motors have been created by chemists that yield rotation, possibly generating torque. == Organelle and vesicle transport ==

There are two major families of molecular motors that transport organelles throughout the cell. These families include the dynein family and the kinesin family. Both have very different structures from one another and different ways of achieving a similar goal of moving organelles around the cell. These distances, though only few micrometers, are all preplanned out using microtubules. • Kinesin These molecular motors always move towards the positive end of the cell • Uses ATP hydrolysis during the process converting ATP to ADP • This process consists of ... • The "foot" of the motor binds using ATP, the "foot" proceeds a step, and then ADP comes off. This repeats itself until the destination has been reached • The kinesin family consists of a multitude of different motor types • Kinesin-1 (Conventional) • Kinesin-2 (Heterotrimeric) • Kinesin-5 (Bipolar) • Kinesin-13 • Dynein These molecular motors always move towards the negative end of the cell • Uses ATP hydrolysis during the process converting ATP to ADP • Unlike kinesin, the dynein is structured in a different way which requires it to have different movement methods. • One of these methods includes the power stroke, which allows the motor protein to "crawl" along the microtubule to its location. • The structure of dynein consists of • A Stem Containing • A region that binds to dynactin • Intermediate/light chains that will attach to the dynactin bonding region • A Head • A Stalk • With a domain that will bind to the microtubule :::::These molecular motors tend to take the path of the microtubules. This is most likely due to the facts that the microtubules spring forth out of the centrosome and surround the entire volume of the cell. This in turn creates a "Rail system" of the whole cell and paths leading to its organelles. == Theoretical considerations ==

Because the motor events are stochastic, molecular motors are often modeled with the Fokker–Planck equation or with Monte Carlo methods. These theoretical models are especially useful when treating the molecular motor as a Brownian motor. == Experimental observation ==

In experimental biophysics, the activity of molecular motors is observed with many different experimental approaches, among them: • Fluorescent methods: fluorescence resonance energy transfer (FRET), fluorescence correlation spectroscopy (FCS), total internal reflection fluorescence (TIRF). • Magnetic tweezers can also be useful for analysis of motors that operate on long pieces of DNA. • Neutron spin echo spectroscopy can be used to observe motion on nanosecond timescales. • Optical tweezers (not to be confused with molecular tweezers in context) are well-suited for studying molecular motors because of their low spring constants. • Scattering techniques: single particle tracking based on dark field microscopy or interferometric scattering microscopy (iSCAT) • Single-molecule electrophysiology can be used to measure the dynamics of individual ion channels. Many more techniques are also used. As new technologies and methods are developed, it is expected that knowledge of naturally occurring molecular motors will be helpful in constructing synthetic nanoscale motors. == Non-biological ==

Recently, chemists and those involved in nanotechnology have begun to explore the possibility of creating molecular motors de novo. These synthetic molecular motors currently suffer many limitations that confine their use to the research laboratory. However, many of these limitations may be overcome as our understanding of chemistry and physics at the nanoscale increases. One step toward understanding nanoscale dynamics was made with the study of catalyst diffusion in the Grubb's catalyst system. Other systems like the nanocars, while not technically motors, are also illustrative of recent efforts towards synthetic nanoscale motors. Other molecules can also behave as motors. Dye molecules can move directionally in gradients of polymer solution through favorable hydrophobic interactions. Another recent study has shown that dye molecules, hard and soft colloidal particles are able to move through gradient of polymer solution through excluded volume effects. == See also ==