z-logo
Premium
Single‐Particle Tracking: Single‐Particle Tracking of Hepatitis B Virus‐like Vesicle Entry into Cells (Small 9/2011)
Author(s) -
Hao Xian,
Shang Xin,
Wu Jiazhen,
Shan Yuping,
Cai Mingjun,
Jiang Junguang,
Huang Zhong,
Tang Zhiyong,
Wang Hongda
Publication year - 2011
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201190028
Subject(s) - endocytosis , hbsag , vesicle , hepatitis b virus , endocytic cycle , microbiology and biotechnology , virology , motility , actin , virus , biophysics , endosome , biology , chemistry , cell , membrane , biochemistry , intracellular
The cover image shows the visualization of the entry of a Hepatitis B virus‐like vesicle (HBsAg) into a cell. HBsAg (shown as red particles) is used as a model to study the infection mechanisms and dynamics of the single‐enveloped virus in living cells by real‐time fluorescence microscopy. HBsAg is found to enter cells via a caveolin‐mediated endocytic pathway (caveolin: yellow). By tracking individual HBsAg particles in living cells, the anomalously actin‐dependent but not microtubule‐dependent motility of internalized HBsAg particles is revealed (actin: green). The motility of HBsAg particles in living cells was also analyzed quantitatively. The results may potentially settle the long‐term debate of whether hepatitis B viruses directly break the plasma membrane barrier or rely on endocytosis to infect the cell. For more information, please read the Full Paper “Single‐Particle Tracking of Hepatitis B Virus‐like Vesicle Entry into Cells” by Z. Huang, Z. Tang, H. Wang, and co‐workers, beginning on page 1212 .

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom