Molecular Structure and Surface Properties of Comb-Like Fluorinated Poly(oxyethylene)s Having Different Content of Fluoroalkyl Side Group

2010 ◽  
Vol 43 (24) ◽  
pp. 10481-10489 ◽  
Author(s):  
Jae-Seung Chung ◽  
Byoung Gak Kim ◽  
Eun-Ho Sohn ◽  
Jong-Chan Lee
2018 ◽  
Vol 115 (12) ◽  
pp. E2696-E2705 ◽  
Author(s):  
Jiahe Li ◽  
Connie Wu ◽  
Wade Wang ◽  
Yanpu He ◽  
Elad Elkayam ◽  
...  

Small interfering RNA (siRNA) represents a promising class of inhibitors in both fundamental research and the clinic. Numerous delivery vehicles have been developed to facilitate siRNA delivery. Nevertheless, achieving highly potent RNA interference (RNAi) toward clinical translation requires efficient formation of RNA-induced gene-silencing complex (RISC) in the cytoplasm. Here we coencapsulate siRNA and the central RNAi effector protein Argonaute 2 (Ago2) via different delivery carriers as a platform to augment RNAi. The physical clustering between siRNA and Ago2 is found to be indispensable for enhanced RNAi. Moreover, by utilizing polyamines bearing the same backbone but distinct cationic side-group arrangements of ethylene diamine repeats as the delivery vehicles, we find that the molecular structure of these polyamines modulates the degree of siRNA/Ago2-mediated improvement of RNAi. We apply this strategy to silence the oncogene STAT3 and significantly prolong survival in mice challenged with melanoma. Our findings suggest a paradigm for RNAi via the synergistic coassembly of RNA with helper proteins.


2015 ◽  
Vol 132 ◽  
pp. 45-53 ◽  
Author(s):  
M. Jarpa-Parra ◽  
F. Bamdad ◽  
Z. Tian ◽  
Hongbo Zeng ◽  
Feral Temelli ◽  
...  

Soft Matter ◽  
2020 ◽  
Vol 16 (30) ◽  
pp. 7063-7076
Author(s):  
Polina Naidjonoka ◽  
Monica Arcos Hernandez ◽  
Gunnar K. Pálsson ◽  
Frank Heinrich ◽  
Henrik Stålbrand ◽  
...  

The relation between bulk and surface properties of hemicelluloses is investigated in order to shed light on the hemicellulose/cellulose interactions.


2021 ◽  
Vol 28 ◽  
Author(s):  
Sen Tang ◽  
Junsheng Li ◽  
Guoxia Huang ◽  
Liujuan Yan

: This article reviews and discusses the relationship between surface hydrophobicity and other surface properties of proteins and the possibility of using surface hydrophobicity as a key indicator to predict and evaluate the changes in the surface properties of a protein. Hydrophobicity is the main driving force of protein folding; it affects the structure and functions. Surface hydrophobicity and other surface properties of proteins are controlled by their spatial structures. Due to the hydrophobic interactions, most proteins fold into their globular structures, and they lack sufficient hydrophobic residues on the molecular surface; thus, they do not exhibit excellent surface properties. Surface hydrophobicity is closely related to the changes in the surface property of proteins because it directly reflects the actual distribution of the hydrophobic residues on the surface of a protein. The molecular structure of a protein can be changed or modified to remove the constraints of spatial structures and expose more hydrophobic residues on the molecular surface, which may improve the surface properties of proteins. Therefore, the changes in the surface hydrophobicity caused by changes in the molecular structure can be an ideal key indicator to predict and evaluate the changes in the surface properties of a protein.


Author(s):  
Rémy Bois ◽  
Isabelle Pezron ◽  
Patricia Rotureau ◽  
Elisabeth Van Hecke ◽  
Guillaume Fayet ◽  
...  

Author(s):  
James E. Mark ◽  
Harry R. Allcock ◽  
Robert West

Polyphosphazenes comprise by far the largest class of inorganic macromolecules. At least 700 different polymers of this type have been synthesized, with a range of physical and chemical properties that rivals that known hitherto only for synthetic organic macromolecules. Most polyphosphazenes have the general molecular structure. The polymer backbone consists of alternating phosphorus and nitrogen atoms, with two side groups, R, being attached to each phosphorus. The side groups may be organic, organometallic, or inorganic units. Each macromolecule typically contains from 100 to 15,000 or more repeating units linked end to end, which means that (depending on the organic side groups) the highest molecular weights are in the range of 2 million to 10 million. The bonding structure in the backbone is formally represented as a series of alternating single and double bonds. However, this formulation is misleading. Structural measurements suggest that all the bonds along the chain are equal or nearly equal in length, but without the extensive conjugation found in organic polyunsaturated materials. This anomaly will be discussed later. In addition to linear polyphosphazenes with one type of side group, other molecular architectures have also been assembled. These include polyphosphazenes in which two or more different side groups, R1 and R2, are arrayed along the chain in random, regular, or block distributions. Other species exist with short phosphazene branches linked to phosphorus atoms in the main chain. Also available are macromolecules in which carbon or sulfur replace some of the phosphorus atoms in the skeleton. Star-geometry structures, using the symbolism defined, are also accessible. A new and growing area is the field of phosphazene-organic and phosphazene-polysiloxane hybrid linear copolymers, and comb copolymers of the types. In addition, polymers are known in which six-membered phosphazene rings are side groups linked to organic polymers, and where phosphazene rings are linked by organic connector groups to form cyclolinear or cyclomatrix materials.


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