Product Uses Include
Eukaryotic kinesin motor proteins orchestrate a wide range of kinetic events within a cell. They have been shown to move cargoes, such as chromosomes and vesicles, along microtubule tracks (1). They also play a major role in the organization of cytoskeletal architecture as evidenced in the establishment of the microtubule spindle during mitosis (2).
Kinesins operate by utilizing the energy of ATP hydrolysis to move along their microtubule (MT) substrates. Once a kinesin motor binds to its MT track, the ATPase rate of the motor is often enhanced several hundred to several thousand fold (3). MT activated kinesin ATPase is a major parameter in motor function and serves as a powerful method to monitor and study kinesin activity under various experimental conditions.
As part of its Cytoskeleton Motor Werks (CMW) line of research reagents, Cytoskeleton, Inc. has developed the Kinesin ELIPA™ (Enzyme Linked Inorganic Phosphate Assay) Biochem Kit. The assay is an adaptation of a method originally described by Webb for the measurement of glycerol kinase plus D-glyceraldehyde ATPase activity and for actin activated myosin ATPase (4). The assay is based upon an absorbance shift (330 - 360 nm) that occurs when 2-amino-6-mercapto-7-methylpurine ribonucleoside (MESG) is catalytically converted to 2-amino-6-mercapto-7-methyl purine in the presence of inorganic phosphate (Pi). The reaction is catalyzed by purine nucleoside phosphorylase (PNP). One molecule of inorganic phosphate will yield one molecule of 2-amino-6-mercapto-7-methyl purine in an essentially irreversible reaction (5). Thus, the absorbance at 360 nm is directly proportional to the amount of Pi generated in the kinesin ATPase reaction.
End point assays for kinesin MT activated ATPase activity in high throughput format can be performed with Biochem Kit™ BK053. Cytoskeleton, Inc. also offers a wide range of kinesin motors (see the Cytoskeleton Motor Werks page).
The kit contains sufficient material for 96 assays. The following components are included:
Figure 1. Microtubule activated kinesin ATPase activity as measured with BK060. The ATPase activities of a selection of kinesin motors was measured. The Vmax for ATP hydrolysis ranges from 10,000 nmol ATP/min/mg for Kinesin HC to 470 nmol ATP/min/mg for Chromokinesin.
I.M. Larrayoz and A. Martinez. 2012. Proadrenomedullin N-terminal 20 peptide increases kinesin's velocity both in vitro and in vivo. Endocrinology. 153, 1734-1742.
C.J. Funk et al. 2004. Development of high-throughput screens for discovery of kinesin adenosine triphosphatase modulators. Anal. Biochem. 329, 68-76.
Question 1: Which kinesin motor proteins can be used in the Kinesin ELIPA Biochem Kit (Cat # BK060)?
Answer 1: The Kinesin ELIPA Biochem Kit (Cat. # BK060) can be used with any of the other kinesin motor proteins sold by Cytoskeleton, Inc. Please see the protein’s datasheet on our website (http://www.cytoskeleton.com/pdf-storage/datasheets/BK060.pdf) for representative data detailing each motor protein’s ATPase activity using either this kit (Cat. # BK053) or our Kinesin ELIPA Biochem Kit (Cat. # BK060).
Question 2: Are there specific requirements of the spectrophotometer that I will use to measure the inorganic phosphate production with the Kinesin ELIPA Biochem Kit (Cat # BK060)?
Answer 2: The assay is based upon an absorption shift from 340 nm to 360 nm. It is therefore very important to use a spectrophotometer that has a narrow bandwidth in order that the wavelength for reading the assay does not encroach upon the 340 nm range. It is recommended that a monochromatic spectrophotometer such as a SpectroMax 350 (Molecular Devices) be used when possible as the bandwidth in these machines is very narrow (2-5 nm). If a filter based system is being used then it is important to make sure that the filter bandwidth is 10 nm or less, if not the result will be a) significant background noise and b) greatly reduced sensitivity of the assay. The spectrophotometer should be at room temperature and set on kinetic mode and it is recommended to take a reading once every 30 seconds. There is no need to elect a blank well as the reaction minus motor will serve as a background control. Do not preread the microtiter plate. Start the kinetic readings at time zero.