MKLP kinesin motor domain protein (KIF23): GST tagged: Homo sapiens recombinant

MKLP kinesin motor domain protein: GST tagged: Homo sapiens recombinant

Product uses

  • Measurement of microtubule-activated ATPase activity
  • Identification/characterization of proteins or small molecules that affect motor ATPase activity
  • Identification/characterization of proteins or small molecules that affect kinesin motility
  • Identification/characterization of proteins or small molecules that affect motor/microtubule interactions

The conserved motor domain of human MKLP1 (KIF23) was expressed in a prokaryotic system. The recombinant protein contains a GSTTag at the amino terminal end and has a combined molecular weight of 82 kD. The protein has been determined to be biologically active in a microtubule-activated ATPase activity test. The protein is supplied as a lyophilized powder.

Protein purity is estimated by scanning densitometry of a coomassie-stained SDS-PAGE gradient gel. Figure 1 shows 10 ug of MP01 protein and purity was determined to be >70%. The total protein in each tube will therefore be approximately 30% greater than the amount shown on the tube. The major contaminant at approximately 30 kD is GST protein. The microtubule-activated ATPase activity of the MKLP1 motor is not inhibited by this contaminant. 

Figure 1. MKLP1 Motor Domain protein gel. A 10 ug sample of recombinant MKLP1 Motor Domain protein (GST-tagged) was separated on a 4-20% SDS-PAGE gradient gel, along with Mark12 molecular weight markers (Invitrogen). The fusion protein runs at 70 kD on the polyacrylamide gradient gel.

Biological Activity - Microtubule Activated ATPase Assay
MKLP1 ATPase activity was measured by monitoring real time free phosphate generation using the Kinesin ELIPA Assay Kit (cat.# BK060). The assay is based upon an absorbance shift (330 nm - 360 nm) that occurs when 2-amino-6-mercapto-7methylpurine ribonucleoside (MESG) is catalytically converted to 2-amino-6-mercapto-7-methylpurine in the presence of inorganic phosphate (Pi). One molecule of Pi will yield one molecule of 2amino-6-mercapto-7-methylpurine in an essentially irreversible reaction. Hence, the absorbance at 360 nm is directly proportional to the amount of Pi generated in the kinesin ATPase reaction. Under the conditions outlined below, the Vmax for MKLP1 microtubule-activated ATPase activity for this Lot was 1000 nmoles ATP generated per minute per mg of MP01 (Figure 2). The ATPase rate for this Lot using a 10 minute endpoint assay (Kinesin ATPase End Point Assay Kit, cat.# BK053) was 600 nmoles ATP per minute per mg of MP01. Both of these values are above the guaranteed minimum.


Figure 2. MP01 microtubule-activated ATPase activity using Kinesin ELIPA Assay Kit (Cat.# BK060).

For product Datasheets and MSDSs please click on the PDF links below.   For additional information, click on the FAQs tab above or contact our Technical Support department at

AuthorTitleJournalYearArticle Link
Funk, C. Joel et al.Development of high-throughput screens for discovery of kinesin adenosine triphosphatase modulatorsAnalytical Biochemistry2004ISSN 0003-2697
Wada, Yuuko et al.Evidence for a Novel Affinity Mechanism of Motor-assisted Transport Along MicrotubulesMolecular Biology of the Cell2000ISSN 1059-1524
Endow, Sharyn A. et al.Determinants of Kinesin Motor PolarityScience1998ISSN 0036-8075

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