A kinesin is a protein belonging to a class of motor proteins found in eukaryotic cells. Kinesins move along microtubule filaments, and are powered by the hydrolysis of ATP (thus kinesins are ATPases). The active movement of kinesins supports several cellular functions including mitosis, meiosis and transport of cellular cargo, such as in axonal transport. Most kinesins walk towards the plus end of a microtubule, which, in most cells, entails transporting cargo from the centre of the cell towards the periphery. This form of transport is known as anterograde transport.
Kinesins were discovered as microtubule (MT)-based anterograde intracellular transport motors. The founding member of this superfamily, kinesin-1, was isolated as a heterotetrameric fast axonal organelle transport motor consisting of 2 identical motor subunits (KHC) and 2 "light chains" (KLC) via microtubule affinity purification from neuronal cell extracts. Subsequently a different, heterotrimeric plus-end-directed MT-based motor named kinesin-2, consisting of 2 distinct KHC-related motor subunits and an accessory "KAP" subunit, was purified from echinoderm egg/embryo extracts and is best known for its role in transporting protein complexes (IFT particles) along axonemes during cilium biogenesis. Molecular genetic and genomic approaches have led to the recognition that the kinesins form a diverse superfamily of motors that are responsible for multiple intracellular motility events in eukaryotic cells. For example, the genomes of mammals encode more than 40 kinesin proteins, organized into at least 14 families named kinesin-1 through kinesin-14.
Members of the kinesin superfamily vary in shape but the prototypical kinesin-1 is a heterotetramer whose motor subunits (heavy chains or KHCs) form a protein dimer (molecule pair) that binds two light chains (KLCs).
The heavy chain of kinesin-1 comprises a globular head (the motor domain) at the amino terminal end connected via a short, flexible neck linker to the stalk – a long, central alpha-helical coiled-coil domain – that ends in a carboxy terminal tail domain which associates with the light-chains. The stalks of two KHCs intertwine to form a coiled-coil that directs dimerization of the two KHCs. In most cases transported cargo binds to the kinesin light chains, but in some cases cargo binds to the C-terminal domains of the heavy chains.
Kinesin motor domain
Kinesin motor domain Crystallographic structure of the human kinesin motor domain depicted as a rainbow colored cartoon (N-terminus = blue, C-terminus = red) complexed with ADP (stick diagram, carbon = white, oxygen = red, nitrogen = blue, phosphorus = orange) and a magnesium ion (grey sphere). Identifiers Symbol Kinesin motor domain Pfam PF00225 InterPro IPR001752 SMART SM00129 PROSITE PS50067 SCOP 1bg2 Available protein structures: Pfam structures PDB RCSB PDB; PDBe PDBsum structure summary
The head is the signature of kinesin and its amino acid sequence is well conserved among various kinesins. Each head has two separate binding sites: one for the microtubule and the other for ATP. ATP binding and hydrolysis as well as ADP release change the conformation of the microtubule-binding domains and the orientation of the neck linker with respect to the head; this results in the motion of the kinesin. Several structural elements in the head, including a central beta-sheet domain and the Switch I and II domains, have been implicated as mediating the interactions between the two binding sites and the neck domain. Kinesins are related structurally to G proteins, which hydrolyze GTP instead of ATP. Several structural elements are shared between the two families, notably the Switch I and Switch II domains.
In the cell, small molecules such as gases and glucose diffuse to where they are needed. Large molecules synthesised in the cell body, intracellular components such as vesicles, and organelles such as mitochondria are too large (and the cytosol too crowded) to diffuse to their destinations. Motor proteins fulfill the role of transporting large cargo about the cell to their required destinations. Kinesins are motor proteins that transport such cargo by walking unidirectionally along microtubule tracks hydrolysing one molecule of adenosine triphosphate (ATP) at each step. It was thought that ATP hydrolysis powered each step, the energy released propelling the head forwards to the next binding site. However, it has been proposed that the head diffuses forward and the force of binding to the microtubule is what pulls the cargo along.
Direction of motion
Motor proteins travel in a specific direction along a microtubule. This is because the microtubule is polar and the heads only bind to the microtubule in one orientation, while ATP binding gives each step its direction through a process known as neck linker zippering.
Most kinesins walk towards the plus end of a microtubule which, in most cells, entails transporting cargo from the centre of the cell towards the periphery. This form of transport is known as anterograde transport. Kinesin-14 family proteins, such as Drosophila NCD, budding yeast KAR3, and Arabidopsis ATK5, walk in the opposite direction, toward microtubule minus ends.
A different type of motor protein known as dyneins, move towards the minus end of the microtubule. Thus they transport cargo from the periphery of the cell towards the centre, for example from the terminal buttons of a neuronal axon to the cell body (soma). This is known as retrograde transport.
Proposed mechanisms of movement
Kinesin accomplishes transport by "walking" along a microtubule. Two mechanisms have been proposed to account for this movement.
- In the "hand-over-hand" mechanism, the kinesin heads step past one another, alternating the lead position.
- In the "inchworm" mechanism, one kinesin head always leads, moving forward a step before the trailing head catches up.
ATP binding and hydrolysis cause kinesin to travel via a "seesaw mechanism" about a pivot point.
Theoretical modeling of kinesin
A number of theoretical models of the molecular motor protein Kinesin have been proposed. Many challenges are encountered in theoretical investigations given the remaining uncertainties about the roles of protein structures, precise way energy from ATP is transformed into mechanical work, and the roles played by thermal fluctuations. This is a rather active area of research. There is a need especially for approaches which better make a link with the molecular architecture of the protein and data obtained from experimental investigations.
Kinesin and mitosis
In recent years, it has been found that microtubule-based molecular motors (including a number of kinesins) have a role in mitosis (cell division). Kinesins are important for proper spindle length and are involved in sliding microtubules apart within the spindle during prometaphase and metaphase, as well as depolymerizing microtubule minus ends at centrosomes during anaphase. Specifically, Kinesin-5 family proteins act within the spindle to slide microtubules apart, while the Kinesin 13 family act to depolymerize microtubules.
Kinesin Superfamily members
Human kinesin superfamily members include the following proteins, which in the standardized nomenclature developed by the community of kinesin researchers, are organized into 14 families named kinesin-1 through kinesin-14:
- 1A – KIF1A, 1B – KIF1B = kinesin-3
- 2A – KIF2A, 2C – KIF2C = kinesin-13
- 3B – KIF3B, 3C – KIF3C = kinesin-2
- 4A – KIF4A, 4B – KIF4B = kinesin-4
- 5A – KIF5A, 5B – KIF5B, 5C – KIF5C = kinesin-1
- 6 – KIF6 = kinesin-9
- 7 – KIF7 = kinesin-4
- 9 – KIF9 = kinesin-9
- 11 – KIF11 = kinesin-5
- 12 – KIF12 = kinesin-12
- 13A – KIF13A, 13B – KIF13B = kinesin-3
- 14 – KIF14 = kinesin-3
- 15 – KIF15 = kinesin-12
- 16B – KIF16B = kinesin-3
- 17 – KIF17 = kinesin-2
- 18A – KIF18A, 18B – KIF18B = kinesin-8
- 19 – KIF19 = kinesin-8
- 20A – KIF20A, 20B – KIF20B = kinesin-6
- 21A – KIF21A, 21B – KIF21B = kinesin-4
- 22 – KIF22 = kinesin-10
- 23 – KIF23 = kinesin-6
- 24 – KIF24 = kinesin-13
- 25 – KIF25 = kinesin-14
- 26A – KIF26A, 26B – KIF26B = kinesin-11
- 27 – KIF27 = kinesin-4
- C1 – KIFC1, C2 – KIFC2, C3 – KIFC3 = kinesin-14
kinesin-1 light chains:
kinesin-2 associated protein:
- KAP-1, KAP3 or KIFAP3
- Axoplasmic transport
- Intraflagellar transport along cilia
- Kinesin 8
- Kinesin 13
- Molecular motors
- Transport by Multiple Kinesin
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- Animated model of kinesin walking
- Ron Vale's iBioSeminars on Motor Proteins
- Animation of kinesin movement ASCB image library
- Kinesin and Dynein Microtubule Movement
- The Inner Life of a Cell, 3D animation featuring a Kinesin transporting a vesicle
- The Kinesin Homepage
- MeSH Kinesin
- EC 188.8.131.52
- EC 184.108.40.206
Proteins of the cytoskeleton HumanI (MYO1A, MYO1B, MYO1C, MYO1D, MYO1E, MYO1F, MYO1G, MYO1H) · II (MYH1, MYH2, MYH3, MYH4, MYH6, MYH7, MYH7B, MYH8, MYH9, MYH10, MYH11, MYH13, MYH14, MYH15, MYH16) · III (MYO3A, MYO3B) · V (MYO5A, MYO5B, MYO5C) · VI (MYO6) · VII (MYO7A, MYO7B) · IX (MYO9A, MYO9B) · X (MYO10) · XV (MYO15A) · XVIII (MYO18A, MYO18B) · LC (MYL1, MYL2, MYL3, MYL4, MYL5, MYL6, MYL6B, MYL7, MYL9, MYLIP, MYLK, MYLK2, MYLL1)OtherOtherEpithelial keratins
(soft alpha-keratins)Hair keratins
(hard alpha-keratins)Ungrouped alphaNot alphaType 3Type 4Type 5KinesinsOtherOther
Nonhuman Hydrolases: acid anhydride hydrolases (EC 3.6) 3.6.1 3.6.2 3.6.3-4: ATPase3.6.3Cu++ (220.127.116.11)Ca+ (18.104.22.168)Na+/K+ (22.214.171.124)H+/K+ (126.96.36.199)ATP4AOther P-type ATPase3.6.4 3.6.5: GTPase188.8.131.52: Heterotrimeric G protein184.108.40.206: Small GTPase > Ras superfamily220.127.116.11: Protein-synthesizing GTPase18.104.22.168-6: Polymerization motors
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