Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

6.5K
The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
6.5K
Protein Kinases and Phosphatases02:54

Protein Kinases and Phosphatases

15.7K
Proteins undergo chemical modifications that trigger changes in the charge, structure, and conformation of the proteins. Phosphorylation, acetylation, glycosylation, nitrosylation, ubiquitination, lipidation, methylation, and proteolysis are various protein modifications that regulate protein activity. Such modifications are usually enzyme-driven.
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
15.7K
Protein Kinases and Phosphatases02:54

Protein Kinases and Phosphatases

4.7K
4.7K
Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

19.7K
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
19.7K
Phosphorylation01:02

Phosphorylation

55.8K
The addition or removal of phosphate groups from proteins is the most common chemical modification that regulates cellular processes. These modifications can affect the structure, activity, stability, and localization of proteins within cells as well as their interactions with other proteins.
During phosphorylation, protein kinases transfer the terminal phosphate group of ATP to specific amino acid side chains of substrate proteins. Serine, threonine, and tyrosine are the most commonly...
55.8K
M-Cdk Drives Transition Into Mitosis02:15

M-Cdk Drives Transition Into Mitosis

6.8K
Checkpoints throughout the cell cycle serve as safeguards and gatekeepers, allowing the cell cycle to progress in favorable conditions and slow or halt it in problematic ones. This regulation is known as the cell cycle control system.
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
6.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Two epithelial cell invasion-related loci of the oral pathogen Actinobacillus actinomycetemcomitans.

Oral microbiology and immunology·2003
Same author

MglA and mglB of Treponema denticola; similarity to ABC transport and spa genes.

DNA sequence : the journal of DNA sequencing and mapping·2001
Same author

The function of interdomain interactions in controlling nucleotide exchange rates in transducin.

The Journal of biological chemistry·2001
Same author

A protein kinase C site highly conserved in P2X subunits controls the desensitization kinetics of P2X(2) ATP-gated channels.

The Journal of biological chemistry·2000
Same author

Functional and biochemical evidence for heteromeric ATP-gated channels composed of P2X1 and P2X5 subunits.

The Journal of biological chemistry·1999
Same author

The porphyromonas gingivalis prtP/kgp homologue exists as two open reading frames in strain 381.

Oral diseases·1999

Related Experiment Video

Updated: Apr 18, 2026

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

19.5K

Understanding the Polo Kinase machine.

V Archambault1, G Lépine1, D Kachaner1

  • 1Institut de recherche en immunologie et en cancérologie, Département de biochimie et médecine moléculaire, Université de Montréal, Montréal, Québec, Canada.

Oncogene
|January 27, 2015
PubMed
Summary

Polo Kinase regulates cell division through its kinase and Polo-Box domains. Understanding its structure and regulation is key for developing anti-cancer drugs targeting cell division.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • Polo Kinase is essential for regulating cell division, including mitosis and cytokinesis.
  • It possesses a kinase domain (KD) and a Polo-Box domain (PBD) that mediate interactions and regulate function.
  • Polo Kinase (Plk1 in humans) is a conserved protein crucial for cell division across organisms.

Purpose of the Study:

  • To review the current understanding of Polo Kinase function and regulation.
  • To explore the structural insights into Polo Kinase's mechanism of action.
  • To discuss the role of Polo Kinase in anti-cancer drug development.

Main Methods:

  • Review of existing literature on Polo Kinase structure and function.
  • Analysis of crystal structures of Polo Kinase domains and complexes.

More Related Videos

A Bilingual Computational Workflow for Identifying Potential PLK1 Inhibitors in American Sign Language and English
14:34

A Bilingual Computational Workflow for Identifying Potential PLK1 Inhibitors in American Sign Language and English

Published on: April 3, 2026

215
Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
11:23

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein

Published on: June 30, 2019

6.8K

Related Experiment Videos

Last Updated: Apr 18, 2026

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

19.5K
A Bilingual Computational Workflow for Identifying Potential PLK1 Inhibitors in American Sign Language and English
14:34

A Bilingual Computational Workflow for Identifying Potential PLK1 Inhibitors in American Sign Language and English

Published on: April 3, 2026

215
Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
11:23

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein

Published on: June 30, 2019

6.8K
  • Examination of molecular mechanisms regulating Polo Kinase activity.
  • Survey of chemical modulators targeting Polo Kinase for therapeutic purposes.
  • Main Results:

    • The PBD and KD cooperate and can mutually inhibit each other's functions.
    • Crystal structures provide insights into the operational mechanisms of Polo Kinase.
    • Numerous molecular mechanisms govern Polo Kinase regulation.
    • Targeting Polo Kinase has led to the development of anti-cancer drug candidates.

    Conclusions:

    • Polo Kinase is a complex molecular device critical for cell division control.
    • Structural and regulatory studies enhance our comprehension of its biological roles.
    • Polo Kinase represents a promising target for novel anti-cancer therapies.