Gold Nanoparticles Help to Develop a New Method for
Tracking Viruses
Researchers
at the Nanoscience Center (NSC) of University of Jyväskylä in Finland have
developed a novel method to study enterovirus structures and their functions.
The method will help to obtain new information on trafficking of viruses in
cells and tissues as well as on the mechanisms of virus opening inside cells.
This new information is important for example for developing new antiviral
drugs and vaccines. The study was published in the journalProceedings of the National Academy of
Science.
Enteroviruses are
pathogenic viruses infecting humans. This group consists of polioviruses,
coxsackieviruses, echoviruses and rhinoviruses. Enteroviruses are the most
common causes of flu, but they also cause serious symptoms such as heart muscle
infections and paralysis. Recently, enteroviruses have been linked with chronic
diseases such as diabetes.
The infection
mechanisms and infectious pathways of enteroviruses are still rather poorly
known. Previous studies in the group of Dr. Varpu Marjomäki at the NSC have
focused on the cellular factors that are important for the infection caused by
selected enteroviruses. The mechanistic understanding of virus opening and the
release of the viral genome in cellular structures for starting new virus
production is still largely lacking. Furthermore, the knowledge of infectious
processes in tissues is hampered by the lack of reliable tools for detecting
virus infection.
The newly developed
method involves a chemical modification of a known thiol-stabilized gold
nanoparticle, the so-called Au102 cluster that was first synthesized and
structurally solved by the group of Roger D Kornberg in 2007 and later
characterized at NSC by the groups of prof. Hannu Häkkinen and prof. Mika
Pettersson in collaboration with Kornberg. The organic thiol surface of the
Au102 particles is modified by attaching linker molecules that make a chemical
bond to sulfur-containing cysteine residues that are part of the surface
structure of the virus. Several tens of gold particles can bind to a single
virus, and the binding pattern shows up as dark tags reflecting the overall
shape and structure of the virus. The gold particles allow for studies on the
structural changes of the viruses during their lifespan.
The study showed also
that the infectivity of the viruses is not compromised by the attached gold
particles which indicates that the labeling method does not interfere with the
normal biological functions of viruses inside cells. This facilitates new
investigations on the virus structures from samples taken from inside cells
during the various phases of the virus infection, and gives possibilities to
obtain new information on the mechanisms of virus uncoating (opening and
release of the genome). The new method allows also for tracking studies of
virus pathways in tissues. This is important for further understanding of acute
and chronic symptoms caused by viruses. Finally, the method is expected to be
useful for developing of new antiviral vaccines that are based on virus-like
particles.
The method was
developed at the NSC as a wide cross-disciplinary collaboration between
chemists, physicists and biologists. Researchers involved in the work are Tanja
Lahtinen, Kirsi Salorinne, Jaakko Koivisto and Mika Pettersson from the
Department of Chemistry, Sami Malola from the Department of Physics and Mari
Martikainen and Varpu Marjomäki from the Department of Biology and
Environmental Science. The research was coordinated by Docent Varpu Marjomäki
and the Scientific Director of NSC, professor Hannu Häkkinen.
The research was
funded by the Academy of Finland and the TEKES FiDiPro -project NOVAC (Novel
methods for vaccination and virus detection).