Related Experiment Video
Updated: Dec 27, 2025

Identification of Kinesin-1 Cargos Using Fluorescence Microscopy
Published on: February 14, 2016
PX Domain-Containing Kinesin KIF16B and Microtubule-Dependent Intracellular Movements
Bo-Jie Li1, Hao Chen2, Su-Su Jiang1
1Department of Biochemistry & Molecular Biology, Medical College, University of South China, Hengyang, 421001, Hunan, China.
Abstract:
As a member of the kinesin-3 family, kinesin family member 16B (KIF16B) has a characteristic PhoX homology (PX) domain that binds to membranes containing phosphatidylinositol-3-phosphate (PI(3)P) and moves along microtubule filaments to the plus end via a process regulated by coiled coils in the stalk region in various cell types. The physiological function of KIF16B supports the transport of intracellular cargo and the formation of endosomal tubules. Ras-related protein (Rab) coordinates many steps of membrane transport and are involved in the regulation of KIF16B-mediated vesicle trafficking. Data obtained from clinical research suggest that KIF16B has a potential effect on the disease processes in intellectual disability, abnormal lipid metabolism, and tumor brain metastasis. In this review, we summarize recent advances in the structural and physiological characteristics of KIF16B as well as diseases associated with KIF16B disorders, and speculating its role as a potential adaptor for intracellular cholesterol trafficking.
Insights
Kinesin family member 16B (KIF16B) transports cellular cargo and forms endosomal tubules. This review explores KIF16B
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Kinesin family member 16B (KIF16B) is a kinesin-3 motor protein.
- It possesses a PhoX homology (PX) domain that binds to PI(3)P-rich membranes.
- KIF16B moves towards microtubule plus ends, regulated by its stalk region's coiled coils.
Purpose of the Study:
- To review recent advances in KIF16B's structural and physiological characteristics.
- To summarize diseases associated with KIF16B dysfunction.
- To speculate on KIF16B's role in intracellular cholesterol trafficking.
Main Methods:
- Literature review of structural and physiological studies on KIF16B.
- Analysis of clinical data linking KIF16B to disease processes.
- Integration of findings on Rab protein regulation of KIF16B-mediated transport.
Main Results:
- KIF16B is crucial for intracellular cargo transport and endosomal tubule formation.
- Rab proteins regulate KIF16B-mediated vesicle trafficking.
- KIF16B dysfunction is implicated in intellectual disability, lipid metabolism disorders, and brain tumor metastasis.
Conclusions:
- KIF16B plays a significant role in membrane transport and cellular organization.
- Disruptions in KIF16B function are linked to various pathological conditions.
- KIF16B may act as a key adaptor in intracellular cholesterol transport pathways.
Related Concept Videos
The Movement of Organelles and Vesicles
Microtubule Associated Motor Proteins
Destabilization of Microtubules
Microtubules in Cell Motility
Anaphase A and B
Plus-end depolymerization releases tubulin heterodimers from the terminal region of the microtubule. As tubulin subunits are lost, the Ndc80 complexes detach...
Intracellular Movement of Viruses and Bacteria

