Product Uses Include
Porcine brain tubulin (>99% pure, see Cat. # T240) has been modified so that random surface lysines contain a covalently linked, long-chain biotin derivative. A long-chain biotin derivative was selected for this procedure because it allows the biotin molecules to be spaced far enough away from the tubulin protein so as not to interfere with its activity, e.g., ligand binding to SPA beads or other streptavidin based reagents. Biotin labeled tubulin is supplied as a lyophilized powder.
Cytoskeleton, Inc. also offers biotinylated cancer cell tubulin (Cat. # H003 )
The protein purity of the tubulin used for labeling is determined by scanning densitometry of Coomassie Blue stained protein on a 4-20% polyacrylamide gel. The protein used for T333P is >99% pure tubulin. Labeled protein is run on an SDS gel, transfered to a nitrocellulose membrane and detected with streptavidin alkaline phosphatase (Fig 1). 10 ng of T333P is readily detectable. No free biotin is detectable in the final product.
Figure 1: Purity determination of biotin tubulin. 10 and 100 ng of T333P was run on a 4-20% SDS-PAGE gel, transferred to a nitrocellulose membrane and biotin labeled material was detected with streptavidin alkaline phosphatase.
The biological activity of T333P is assessed by a tubulin polymerization assay. To pass quality control, a 5 mg/ml solution of fluorescein labeled tubulin in G-PEM plus 5% glycerol must polymerize to >85%. This is comparable to unlabeled tubulin under identical conditions.
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 email@example.com
|Havelka, Daniel et al.||Lab-on-chip microscope platform for electro-manipulation of a dense microtubules network||Scientific Reports||2022||ISSN 2045-2322|
|Kuzmić, Mira et al.||Septin-microtubule association via a motif unique to isoform 1 of septin 9 tunes stress fibers||Journal of Cell Science||2022||ISSN 1477-9137|
|Zheng, Pengli et al.||ER proteins decipher the tubulin code to regulate organelle distribution||Nature||2022||ISSN 1476-4687|
|Chen, Jiayi et al.||Α-Tubulin Tail Modifications Regulate Microtubule Stability Through Selective Effector Recruitment, Not Changes in Intrinsic Polymer Dynamics||Developmental Cell||2021||ISSN 1878-1551|
|Watson, Joseph L. et al.||High-efficacy subcellular micropatterning of proteins using fibrinogen anchors||Journal of Cell Biology||2021||ISSN 1540-8140|
|Cook, Alexander D. et al.||Cryo-EM structure of a microtubule-bound parasite kinesin motor and implications for its mechanism and inhibition||Journal of Biological Chemistry||2021||ISSN 1083-351X|
|Zhernov, Ilia et al.||Intrinsically Disordered Domain of Kinesin-3 Kif14 Enables Unique Functional Diversity||Current Biology||2020||ISSN 1879-0445|
|Rodríguez-García, Ruddi et al.||Mechanisms of Motor-Independent Membrane Remodeling Driven by Dynamic Microtubules||Current Biology||2020||ISSN 1879-0445|
|Zehr, Elena A. et al.||Katanin Grips the β-Tubulin Tail through an Electropositive Double Spiral to Sever Microtubules||Developmental Cell||2020||ISSN 1878-1551|
|Gaska, Ignas et al.||The Mitotic Crosslinking Protein PRC1 Acts Like a Mechanical Dashpot to Resist Microtubule Sliding||Developmental Cell||2020||ISSN 1878-1551|
|Adriaans, Ingrid E. et al.||MKLP2 Is a Motile Kinesin that Transports the Chromosomal Passenger Complex during Anaphase||Current Biology||2020||ISSN 1879-0445|
|Peña, Alejandro et al.||Structure of Microtubule-Trapped Human Kinesin-5 and Its Mechanism of Inhibition Revealed Using Cryoelectron Microscopy||Structure||2020||ISSN 1878-4186|
|Aher, Amol et al.||CLASP Mediates Microtubule Repair by Restricting Lattice Damage and Regulating Tubulin Incorporation||Current Biology||2020||ISSN 1879-0445|
|Li, Feiran et al.||Local direction change of surface gliding microtubules||Biotechnology and Bioengineering||2019||ISSN 1097-0290|
|Chudinova, Elena M. et al.||On the interaction of ribosomal protein RPL22e with microtubules||Cell Biology International||2019||ISSN 1095-8355|
|Nakos, Konstantinos et al.||Regulation of microtubule plus end dynamics by septin 9||Cytoskeleton||2019||ISSN 1949-3592|
|Faltova, Lenka et al.||Crystal Structure of a Heterotetrameric Katanin p60:p80 Complex||Structure||2019||ISSN 1878-4186|
|Nakos, Konstantinos et al.||Septin 2/6/7 complexes tune microtubule plus-end growth and EB1 binding in a concentration- And filament-dependent manner||Molecular Biology of the Cell||2019||ISSN 1939-4586|
|Hu, Yuhan et al.||Regulation of MT dynamics via direct binding of an Abl family kinase||Journal of Cell Biology||2019||ISSN 1540-8140|
|Siddiqui, Nida et al.||PTPN21 and Hook3 relieve KIF1C autoinhibition and activate intracellular transport||Nature Communications||2019||ISSN 2041-1723|
|McClintock, Mark A. et al.||RNA-directed activation of cytoplasmic dynein-1 in reconstituted transport RNPs||eLife||2018||ISSN 2050-084X|
|Reinemann, Dana N. et al.||Processive Kinesin-14 HSET Exhibits Directional Flexibility Depending on Motor Traffic||Current Biology||2018||ISSN 0960-9822|
|Fan, Yuanwei et al.||The Arabidopsis SPIRAL2 Protein Targets and Stabilizes Microtubule Minus Ends||Current Biology||2018||ISSN 0960-9822|
|Karasmanis, Eva P. et al.||Erratum: Polarity of Neuronal Membrane Traffic Requires Sorting of Kinesin Motor Cargo during Entry into Dendrites by a Microtubule-Associated Septin (Developmental Cell (2018) 46(2) (204–218.e7), (S1534580718304982) (10.1016/j.devcel.2018.06.013))||Developmental Cell||2018||ISSN 1878-1551|
|Aher, Amol et al.||CLASP Suppresses Microtubule Catastrophes through a Single TOG Domain||Developmental Cell||2018||ISSN 1878-1551|
|Pesenti, Marion E. et al.||Reconstitution of a 26-Subunit Human Kinetochore Reveals Cooperative Microtubule Binding by CENP-OPQUR and NDC80||Molecular Cell||2018||ISSN 1097-4164|
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|Rao, Lu et al.||Combining structure–function and single-molecule studies on cytoplasmic dynein||Methods in Molecular Biology||2018||ISSN 1064-3745|
|McIntosh, Betsy B. et al.||Opposing Kinesin and Myosin-I Motors Drive Membrane Deformation and Tubulation along Engineered Cytoskeletal Networks||Current Biology||2018||ISSN 0960-9822|
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|Maciejowski, John et al.||Mps1 Regulates Kinetochore-Microtubule Attachment Stability via the Ska Complex to Ensure Error-Free Chromosome Segregation||Developmental Cell||2017||ISSN 1878-1551|
|Arellano-Santoyo, Hugo et al.||A Tubulin Binding Switch Underlies Kip3/Kinesin-8 Depolymerase Activity||Developmental Cell||2017||ISSN 1878-1551|
|Kandel, Mikhail E. et al.||Label-Free Imaging of Single Microtubule Dynamics Using Spatial Light Interference Microscopy||ACS Nano||2017||ISSN 1936-086X|
|Reinemann, Dana N. et al.||Collective Force Regulation in Anti-parallel Microtubule Gliding by Dimeric Kif15 Kinesin Motors||Current Biology||2017||ISSN 0960-9822|
|Britto, Mishan et al.||Schizosaccharomyces pombe kinesin-5 switches direction using a steric blocking mechanism||Proceedings of the National Academy of Sciences of the United States of America||2016||ISSN 1091-6490|
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|Choi, Bo Hwa et al.||Suprafenacine, an Indazole-Hydrazide Agent, Targets Cancer Cells Through Microtubule Destabilization||PLOS ONE||2014||ISSN 1932--6203|
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|DeBerg, Hannah A. et al.||Motor domain phosphorylation modulates kinesin-1 transport||Journal of Biological Chemistry||2013||ISSN 0021-9258|
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|Yang, Yali et al.||Microrheology of highly crosslinked microtubule networks is dominated by force-induced crosslinker unbinding||Soft Matter||2013||ISSN 1744-683X|
|Leslie, Kris et al.||Going Solo: Measuring the motions of microtubules with an in vitro assay for tirf microscopy.||Methods in Cell Biology||2013||ISSN 0091-679X|
|Kim, Eunji et al.||Electrical control of kinesin-microtubule motility using a transparent functionalized-graphene substrate||Nanotechnology||2013||ISSN 0957-4484|
|He, Siheng et al.||Modeling negative cooperativity in streptavidin adsorption onto biotinylated microtubules||Langmuir||2012||ISSN 0743-7463|
|Choi, Dong Shin et al.||Dual transport systems based on hybrid nanostructures of microtubules and actin filaments||Small||2011||ISSN 1613-6829|
|Dixit, Ram et al.||Studying Plus-End Tracking at Single Molecule Resolution Using TIRF Microscopy||Methods in Cell Biology||2010||ISSN 0091--679X|
|Gell, Christopher et al.||Microtubule Dynamics Reconstituted In Vitro and Imaged by Single-Molecule Fluorescence Microscopy||Methods in Cell Biology||2010||ISSN 0091--679X|
Question 1: What is the proper way to store the tubulin to insure maximum stability and activity?
Answer 1: The recommended storage condition for the lyophilized tubulin product is 4°C with desiccant to maintain humidity at <10% humidity. Under these conditions the protein is stable for 6 months. Lyophilized protein can also be stored desiccated at -70°C where it will be stable for 6 months. However, at -70°C the rubber seal in the lid of the tube could crack and allow in moisture. Therefore we recommend storing at 4°C. If stored at -70°C, it is imperative to include desiccant with the lyophilized protein if this storage condition is utilized. After reconstituting the protein as directed, the concentrated protein in G-PEM buffer should be aliquoted, snap frozen in liquid nitrogen and stored at -70°C (stable for 6 months). NOTE: It is very important to snap freeze the tubulin in liquid nitrogen as other methods of freezing will result in significantly reduced activity. Defrost rapidly by placing in a room temperature water bath for 1 min. Avoid repeated freeze/thaw cycles.
Question 2: Does the biotinylated tubulin polymerize as well as unlabeled tubulin?
Answer 2: Yes, the biotinylated tubulin (Cat. # T333P) polymerizes as well as unlabeled tubulin (Cat. # 240). The biological activity of biotinylated tubulin is determined from its ability to efficiently polymerize into microtubules in vitro and separate from unpolymerized protein in a spin-down assay. Stringent quality control ensures that >85% of the biotinylated tubulin can polymerize in this assay. This is comparable to the polymerization capacity of unmodified tubulin (Cat. # T240).
Question 3: Why does Cytoskeleton recommend the use of general tubulin buffer and GTP for resuspending tubulin?
Answer 3: We recommend resuspending tubulin in general tubulin buffer + GTP to maintain tubulin monomer protein stability and conformation and to provide the necessary components for polymerization. For resuspension, we recommend using a general tubulin buffer (Cat. # BST01-001) which consists of 80 mM PIPES, 2 mM MgCl2, 1 mM EGTA, pH 7.0, supplemented with 1 mM GTP (Cat. # BST06-001). Tubulin requires GTP and magnesium ions for proper stability and conformation, even in its monomeric state. GTP is also required for the polymerization process as its hydrolysis during tubulin polymerization is necessary for polymerization to occur. EGTA is a chelator of calcium which is a potent inhibitor of tubulin polymerization. Glycerol is often added to a final concentration of 5 - 10% to enhance polymerization; however, glycerol is not necessary for the maintenance of biologically active tubulin and does not need to be included when reconstituting and storing tubulin. When aliquoting reconstituted tubulin for storage, it is essential to aliquot and snap-freeze tubulin in liquid nitrogen at a concentration of >6 mg/ml to preserve tubulin’s biological activity. Then the aliquots should be stored at -70°C. When thawing the aliquots, thaw rapidly in a room temperature water bath and place on ice until right before experimental use.
If you have any questions concerning this product, please contact our Technical Service department at firstname.lastname@example.org.