TY - JOUR
T1 - High-efficacy subcellular micropatterning of proteins using fibrinogen anchors
AU - Watson, Joseph L.
AU - Aich, Samya
AU - Oller-Salvia, Benjamí
AU - Drabek, Andrew A.
AU - Blacklow, Stephen C.
AU - Chin, Jason
AU - Derivery, Emmanuel
N1 - Funding Information:
This work has been supported by the Medical Research Council (MC_UP_1201/13 to E. Derivery) and the Human Frontier Science Program (Career Development Award CDA00034/2017-C to E. De-rivery). J.L. Watson is the recipient of a Michael Neuberger Studentship from the Max Perutz Fund and Trinity College, Cambridge.
Publisher Copyright:
© 2021 Crown copyright.
PY - 2021
Y1 - 2021
N2 - Protein micropatterning allows proteins to be precisely deposited onto a substrate of choice and is now routinely used in cell biology and in vitro reconstitution. However, drawbacks of current technology are that micropatterning efficiency can be variable between proteins and that proteins may lose activity on the micropatterns. Here, we describe a general method to enable micropatterning of virtually any protein at high specificity and homogeneity while maintaining its activity. Our method is based on an anchor that micropatterns well, fibrinogen, which we functionalized to bind to common purification tags. This enhances micropatterning on various substrates, facilitates multiplexed micropatterning, and dramatically improves the on-pattern activity of fragile proteins like molecular motors. Furthermore, it enhances the micropatterning of hard-to-micropattern cells. Last, this method enables subcellular micropatterning, whereby complex micropatterns simultaneously control cell shape and the distribution of transmembrane receptors within that cell. Altogether, these results open new avenues for cell biology.
AB - Protein micropatterning allows proteins to be precisely deposited onto a substrate of choice and is now routinely used in cell biology and in vitro reconstitution. However, drawbacks of current technology are that micropatterning efficiency can be variable between proteins and that proteins may lose activity on the micropatterns. Here, we describe a general method to enable micropatterning of virtually any protein at high specificity and homogeneity while maintaining its activity. Our method is based on an anchor that micropatterns well, fibrinogen, which we functionalized to bind to common purification tags. This enhances micropatterning on various substrates, facilitates multiplexed micropatterning, and dramatically improves the on-pattern activity of fragile proteins like molecular motors. Furthermore, it enhances the micropatterning of hard-to-micropattern cells. Last, this method enables subcellular micropatterning, whereby complex micropatterns simultaneously control cell shape and the distribution of transmembrane receptors within that cell. Altogether, these results open new avenues for cell biology.
UR - http://www.scopus.com/inward/record.url?scp=85099703690&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000619488200008&DestLinkType=FullRecord&DestApp=WOS_CPL
UR - http://hdl.handle.net/20.500.14342/3639
U2 - 10.1083/JCB.202009063
DO - 10.1083/JCB.202009063
M3 - Article
C2 - 33416860
AN - SCOPUS:85099703690
SN - 0021-9525
VL - 220
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 2
M1 - e202009063
ER -