Custom micropatterning for cell control
Control the chemistry and topography of cell microenvironment and study their impacts on cell development using an innovative quantitative multi-protein photopatterning solution.
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PRIMO was developed to enable you to design and conduct all the micropatterning experiments you can imagine, in 2D and also 3D.
Simply select the pattern you want to use from your computer files (no size or shape limitations). Primo then projects it onto the cell culture substrate and allows you to generate the pattern with the protein of your choice.
Studying the influence of the microenvironment on intracellular and intercellular mechanisms has been essential for research in cell and medical biology, for many years now.
Among the methods to control this microenvironment is a rapidly developing process called “micropatterning”, which involves creating protein patterns upon which living cells are cultivated. However, current micropatterning techniques are tedious, complex and non-quantitative.
Based on this finding, the scientists at Alvéole developed an innovative multi-protein photopatterning technique to make experimental manipulations easier for researchers.
* «Multiprotein Printing by Light-Induced Molecular Adsorption» Strale P.O. et al, Adv Mater. 2015
The PRIMO technique is based on LIMAP* technology (Light Induced Molecular Adsorption of Proteins) and combines a maskless photolithography system (PRIMO) controlled by a dedicated software (named “Leonardo”) and a specific photoactivatable reagent (PLPP). The combined action of UV and PLPP makes it possible to generate, in only a few seconds, any multi-protein pattern on standard cell culture substrates.
Discover the key steps of PRIMO photopatterning process
An image file is loaded in
Leonardo Software which sends it
to the PRIMO module
PRIMO projects the image
onto the substrate (UV light, λ=375nm).
The pattern results from the
combined action of UV and PLPP
Proteins are added
(fibronectin for example) and bind to
the illuminated areas only.
Cells are seeded
and adhere to the
protein micropatterns only.
over the entire field of view*
for a full field pattern*
for cell culture**
** slides, coverslips, Petri dishes,
3D devices, microfluidic devices, etc.
Sequential photopatterning of Fibrinogen-A488 in green and Protein A-A647 in red onto PDMS micropillars microfabricated with PRIMO.
Epifluorescence microscopy image of 1,5µm dots (spaced by 1,5µm) of ProteinA-488 on PDMS.
Epifluorescence microscopy image of 2µm horizontal lines of ProteinA-488 on glass.
Epifluorescence microscopy image of a gradient of Fibrinogen-A488 on a glass coverslip.
Design and conduct
your own experiment!
Draw, download and project a new image according to your needs!
Use your regular cell culture substrates (flat or microstructured, stiff or soft) without constraints
More than 10 proteins used daily by our users, including
Fibrinogen-488, Fibrinogen-647, Fibronectin, GFP, Neutravidin-488, Neutravidin-647, PLL-PEG-Biotin, Protein A-647, Streptavidin, as well as primary and secondary antibodies.
glass coverslips, glass slides, PDMS, polyacrylamide gel (transfer), polystyrene, UV-curable materials.
“We are working on the generation of 3D cellular microenvironments to reproduce Hematopoietic Niches. PRIMO will be used to generate 3D photo-polymerized microenvironments and to pattern them to localize different cell populations involved in the hematopoiesis.”
“We are currently particularly interested in determining the role of the biophysical environment in the establishment of apico-basal polarity in mammary gland cells and in liver cells. The use of PRIMO in this context proved absolutely essential since it allowed us to create artificial microniches in 3D where we could control up to 150 combinations of environmental cues.”
“Our aim is to develop in vitro experimentation to decipher guiding mechanisms involved in vivo. PRIMO technology is particularly adapted to design in vitro microdevices patterned with controlled patches of the signaling proteins relevant for white blood cell migration.”
“We are interested in imaging subcellular localization of certain cell-surface receptors and check whether they colocalize with focal-adhesion complexes. For this purpose, we are interested in making different types of patterns of Fibronectin with subcellular dimensions.”
“My research project aims at unravelling how a T cell switches from a fast migratory state to a stationary state upon activation. To do so, I perform live cell imaging of T cells migrating inside micro-fabricated channels coated with activating molecules. However, with this approach, I do not control when and where a T cell encounters the activating molecules.”
Our team will be happy to answer any questions you may have.