Key result
A standard gliding motility assay demonstrated that large BSA-free patterns allowed for selective confinement of actin filaments motility on micro- and nano-patterned heavy mero myosin surfaces.
Micro-contact printing of myosin patterns enables the study and control of actin filament motility in nano-confined spaces, which is relevant for the development of hybrid dynamic nanodevices.
Supports nanodevice engineering via confined motility; leaves open in vivo validation and clinical translation.
Protein molecular motors, which convert, directly and efficiently, chemical energy into motion, are excellent candidates for integration in hybrid dynamic nanodevices. To integrate and use the full potential of molecular motors in these devices, their design requires a quantitative and precise prediction of the fundamental mechanical and physicochemical features of cytoskeletal proteins operating in artificial environments. In that regard, the behavior of protein molecular motors constructs in/on nano-confined spaces or nanostructured surfaces that aim to control their motility is of critical interest. Here, we used a standard gliding motility assay to study the actin filaments sliding on a surface comprising heavy mero myosin (HMM) micro- and nano-patterns. To print HMM, we used negative tone, micro contact printing of a blocking protein (bovine serum albumin, BSA) on a nitrocellulose surface, followed by specific adsorption of HMM on BSA-free surfaces. While the large BSA-free patterns allowed for selective confinement of actin filaments motility, the BSA-stamped areas displayed intricate nano-sized HMM patterns, which enabled a deeper analysis of the nano-mechanics of actomyosin motility in confined spaces.
No takes yet. Share an insight, caveat, or question.
Hajne et al. (2015) studied this question. Micro-contact printed heavy mero myosin (HMM) patterns was evaluated on Actin filaments sliding/motility. A standard gliding motility assay demonstrated that large BSA-free patterns allowed for selective confinement of actin filaments motility on micro- and nano-patterned heavy mero myosin surfaces.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: