Characterization of RNA Nanoparticles and Their Dynamic Properties Using Atomic Force Microscopy.

The protocol described in this chapter allows for acquiring topography images of RNA-based nanoring structures and assessing their dynamic properties using atomic force microscopy (AFM) imaging. AFM is an indispensable tool for characterization of nucleic acid-based nanostructures with the exceptional capability of observing complexes in the range of a few nanometers. This method can visualize structural characteristics and evaluate differences between individual structurally different RNA nanorings.

The non-canonical mechanism of ER stress-mediated progression of prostate cancer.

Background: The development of persistent endoplasmic reticulum (ER) stress is one of the cornerstones of prostate carcinogenesis; however, the mechanism is missing. Also, alcohol is a physiological ER stress inducer, and the link between alcoholism and progression of prostate cancer (PCa) is well documented but not well characterized. According to the canonical model, the mediator of ER stress, ATF6, is cleaved sequentially in the Golgi by S1P and S2P proteases; thereafter, the genes responsible for unfolded protein response (UPR) undergo transactivation.

Tuning properties of silver nanoclusters with RNA nanoring assemblies.

Combining atomically resolved DNA-templated silver nanoclusters (AgNCs) with nucleic acid nanotechnology opens new exciting possibilities for engineering bioinorganic nanomaterials with uniquely tunable properties. In this unforeseen cooperation, nucleic acids not only drive the formation of AgNCs but also promote their spatial organization in supra-assemblies. In this work, we confirm the feasibility of this approach using programmable RNA rings to control formation and optical properteis of six individual AgNCs.

Cyclization in bipartite random graphs.

In this paper the time evolution of a finite bipartite graph initially comprising two sorts of isolated vertices is considered. The graph is assumed to evolve by adding edges, one at a time. Each new edge connects either two linked components and forms a new component of a larger order (coalescence of graphs) or increases (by one) the number of edges in a given linked component (cycling).

Post-ER Stress Biogenesis of Golgi Is Governed by Giantin.

Background: The Golgi apparatus undergoes disorganization in response to stress, but it is able to restore compact and perinuclear structure under recovery. This self-organization mechanism is significant for cellular homeostasis, but remains mostly elusive, as does the role of giantin, the largest Golgi matrix dimeric protein.

Methods: In HeLa and different prostate cancer cells, we used the model of cellular stress induced by Brefeldin A (BFA).

Characterization of DNA bound cyclic GMP-AMP synthase using atomic force microscopy imaging.

The protocol described herein allows for acquiring topography images of DNA-protein complexes using Atomic Force Microscopy imaging. Since the very beginning of this method, AFM has been an indispensable tool for characterization of biomolecular complexes with exceptional capability of observing single complexes. This method can visualize structural characteristics of DNA-protein assemblies and evaluate differences between individual complexes.

CRL-based ultra-compact transfocator for X-ray focusing and microscopy.

A new ultra-compact transfocator (UCTF) based on X-ray compound refractive lenses (CRLs) is presented. The device can be used to change the number of one- and two-dimensional focusing CRLs by moving the individual parabolic lenses one-by-one independently, thus providing permanent energy and focal-length tunability for scanning and full-field X-ray microscopy applications. The small overall size and light weight of the device allow it to be integrated in any synchrotron beamline, while even simplifying the experimental layout.

First Step Towards Larger DNA-Based Assemblies of Fluorescent Silver Nanoclusters: Template Design and Detailed Characterization of Optical Properties.

Besides being a passive carrier of genetic information, DNA can also serve as an architecture template for the synthesis of novel fluorescent nanomaterials that are arranged in a highly organized network of functional entities such as fluorescent silver nanoclusters (AgNCs). Only a few atoms in size, the properties of AgNCs can be tuned using a variety of templating DNA sequences, overhangs, and neighboring duplex regions. In this study, we explore the properties of AgNCs manufactured on a short DNA sequence-an individual element designed for a construction of a larger DNA-based functional assembly.

Versatile kit of robust nanoshapes self-assembling from RNA and DNA modules.

DNA and RNA have emerged as a material for nanotechnology applications that take advantage of the nucleic acids' ability to encode folding and programmable self-assembly through mainly base pairing. The two types of nucleic acid have rarely been used in combination to enhance structural diversity or for partitioning of functional and architectural roles. Here, we report a design and screening strategy to integrate combinations of RNA motifs as architectural joints and DNA building blocks as functional modules for programmable self-assembly of a versatile toolkit of polygonal nucleic acid nanoshapes.

Label-free characterization of exosome via surface enhanced Raman spectroscopy for the early detection of pancreatic cancer.

Pancreatic cancer is a highly lethal malignancy. Lack of early diagnostic markers makes timely detection of pancreatic cancer a highly challenging endeavor. Exosomes have emerged as information-rich cancer specific biomarkers.

Dynamic Behavior of RNA Nanoparticles Analyzed by AFM on a Mica/Air Interface.

RNA is an attractive biopolymer for engineering self-assembling materials suitable for biomedical applications. Previously, programmable hexameric RNA rings were developed for the controlled delivery of up to six different functionalities. To increase the potential for functionalization with little impact on nanoparticle topology, we introduce gaps into the double-stranded regions of the RNA rings.

Source-enhanced coalescence of trees in a random forest.

The time evolution of a random graph with varying number of edges and vertices is considered. The edges and vertices are assumed to be added at random by one at a time with different rates. A fresh edge connects either two linked components and forms a new component of larger order g (coalescence of graphs) or increases (by one) the number of edges in a given linked component (cycling).

Exactly solvable model of a coalescing random graph.

An initially empty (no edges) graph of order M evolves by randomly adding one edge at a time. This edge connects either two linked components and forms a new component of larger order (coalescence of graphs) or increases (by one) the number of edges in a given linked component (cycling). Assuming that the vertices of the graph have a finite valence (the number of edges connected with a given vertex is limited) the kinetic equation for the distribution of linked components of the graph over their orders and valences is formulated and solved by applying the generating function method.

Interaction of APOBEC3A with DNA assessed by atomic force microscopy.

The APOBEC3 family of DNA cytosine deaminases functions to block the spread of endogenous retroelements and retroviruses including HIV-1. Potency varies among family members depending on the type of parasitic substrate. APOBEC3A (A3A) is unique among the human enzymes in that it is expressed predominantly in myeloid lineage cell types, it is strongly induced by innate immune agonists such as type 1 interferon, and it has the capacity to accommodate both normal and 5-methyl cytosine nucleobases.

Composition distributions of particles in a gelling mixture.

Gelation in a two component disperse system wherein binary coagulation governs the temporal changes of particle composition spectra is studied for the crossproduct coagulation kernel proportional to m1n2+m2n1, with m,n being the numbers of monomers of the first and the second component in the coalescing pair of particles. This model reveals the sol-gel transition, i.e.

Postcritical behavior of a gelling system.

The formation of a gel in a disperse coagulating system, wherein binary coagulation governs the temporal changes of the particle mass spectrum is studied for the coagulation kernel proportional to K(g,l)=gl with g,l being the numbers of monomers in the coalescing pair of particles. This model is known to reveal the sol-gel transition, i.e.

Atomic force microscopy studies of APOBEC3G oligomerization and dynamics.

The DNA cytosine deaminase APOBEC3G (A3G) is a two-domain protein that binds single-stranded DNA (ssDNA) largely through its N-terminal domain and catalyzes deamination using its C-terminal domain. A3G is considered an innate immune effector protein, with a natural capacity to block the replication of retroviruses such as HIV and retrotransposons. However, knowledge about its biophysical properties and mechanism of interaction with DNA are still limited.

MORPH-PRO: a novel algorithm and web server for protein morphing.

Background: Proteins are known to be dynamic in nature, changing from one conformation to another while performing vital cellular tasks. It is important to understand these movements in order to better understand protein function. At the same time, experimental techniques provide us with only single snapshots of the whole ensemble of available conformations.

Isothermal absorption of soluble gases by atmospheric nanoaerosols.

We investigate mass transfer during the isothermal absorption of atmospheric trace soluble gases by a single droplet whose size is comparable to the molecular mean free path in air at normal conditions. It is assumed that the trace reactant diffuses to the droplet surface and then reacts with the substances inside the droplet according to the first-order rate law. Our analysis applies a flux-matching theory of transport processes in gases and assumes constant thermophysical properties of the gases and liquids.

Supersingular mass distributions in gelling systems.

This paper considers the time evolution of disperse systems in which binary coagulation is so rapid that it leads to formation of gels during a finite but nonzero interval of time. Right before the transition point an algebraic particle mass spectrum forms whose behavior at small particle masses does not permit one to define the total particle mass concentration as ∫(0) (∞)gc(g,t)dg, because the integral diverges at low limit. This divergency prevents the formulation of an asymptotic self-similarity spectrum in its traditional form.

Nanoscale structure and dynamics of ABOBEC3G complexes with single-stranded DNA.

The DNA cytosine deaminase APOBEC3G (A3G) is capable of blocking retrovirus replication by editing viral cDNA and impairing reverse transcription. However, the biophysical details of this host-pathogen interaction are unclear. We applied atomic force microscopy (AFM) and hybrid DNA substrates to investigate properties of A3G bound to single-stranded DNA (ssDNA).

Specificity of binding of single-stranded DNA-binding protein to its target.

Single-stranded DNA-binding proteins (SSBs) bind single-stranded DNA (ssDNA) and participate in all genetic processes involving ssDNA, such as replication, recombination, and repair. Here we applied atomic force microscopy to directly image SSB-DNA complexes under various conditions. We used the hybrid DNA construct methodology in which the ssDNA segment is conjugated to the DNA duplex.

Atomic force microscopy studies provide direct evidence for dimerization of the HIV restriction factor APOBEC3G.

APOBEC3G (A3G) is an antiviral protein that binds RNA and single-stranded DNA (ssDNA). The oligomerization state of A3G is likely to be influenced by these nucleic acid interactions. We applied the power of nanoimaging atomic force microscopy technology to characterize the role of ssDNA in A3G oligomerization.

DNA synapsis through transient tetramerization triggers cleavage by Ecl18kI restriction enzyme.

To cut DNA at their target sites, restriction enzymes assemble into different oligomeric structures. The Ecl18kI endonuclease in the crystal is arranged as a tetramer made of two dimers each bound to a DNA copy. However, free in solution Ecl18kI is a dimer.