Tip-enhanced
Raman scattering (TERS) is a promising optical and
analytical technique for chemical imaging and sensing at single molecule
resolution. In particular, TERS signals generated by a gap-mode configuration
where a silver tip is coupled with a gold substrate can resolve a
single-stranded DNA (ssDNA) molecule with a spatial resolution below
1 nm. To demonstrate the proof of subnanometer resolution, we show
direct nucleic acid sequencing using TERS of a phage ssDNA (M13mp18).
M13mp18 provides a known sequence and, through our deposition strategy,
can be stretched (uncoiled) and attached to the substrate by its phosphate
groups, while exposing its nucleobases to the tip. After deposition,
we scan the silver tip along the ssDNA and collect TERS signals with
a step of 0.5 nm, comparable to the bond length between two adjacent
DNA bases. By demonstrating the real-time profiling of a ssDNA configuration
and furthermore, with unique TERS signals of monomeric units of other
biopolymers, we anticipate that this technique can be extended to
the high-resolution imaging of various nanostructures as well as the
direct sequencing of other important biopolymers including RNA, polysaccharides,
and polypeptides.
The introduction of nanomaterials into cells is an indispensable process for studies ranging from basic biology to clinical applications. To deliver foreign nanomaterials into living cells, traditionally endocytosis, viral and lipid nanocarriers or electroporation are mainly employed; however, they critically suffer from toxicity, inconsistent delivery, and low throughput and are time-consuming and labor-intensive processes. Here, we present a novel inertial microfluidic cell hydroporator capable of delivering a wide range of nanomaterials to various cell types in a single-step without the aid of carriers or external apparatus. The platform inertially focuses cells into the channel center and guides cells to collide at a T-junction. Controlled compression and shear forces generate transient membrane discontinuities that facilitate passive diffusion of external nanomaterials into the cell cytoplasm while maintaining high cell viability. This hydroporation method shows superior delivery efficiency, is high-throughput, and has high controllability; moreover, its extremely simple and low-cost operation provides a powerful and practical strategy in the applications of cellular imaging, biomanufacturing, cell-based therapies, regenerative medicine, and disease diagnosis.
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