Rational design of a fluorescent poly(N-aryleneindole ether sulfone) switch by cation–π interactions

2015 ◽  
Vol 6 (5) ◽  
pp. 697-702 ◽  
Author(s):  
Guanjun Chang ◽  
Li Yang ◽  
Shenye Liu ◽  
Runxiong Lin ◽  
Jingsong You

A fluorescence emission on–off switch is achieved by adjusting the assembly of poly(N-aryleneindole ether sulfone) (PESIN) and pyridine hydrochloride via the cation–π interactions.

2016 ◽  
Vol 4 (7) ◽  
pp. 2517-2523 ◽  
Author(s):  
Guanjun Chang ◽  
Zhenfang Shang ◽  
Tao Yu ◽  
Li Yang

An indole-based microporous organic polymer (PINK) is achieved and it exhibits good performance for carbon dioxide uptake via the local dipole–π interactions.


RSC Advances ◽  
2021 ◽  
Vol 11 (19) ◽  
pp. 11651-11654
Author(s):  
Masaki Takahashi ◽  
Naoya Tsuji ◽  
Kohei Yazaki ◽  
Yoshihisa Sei ◽  
Makoto Obata

Macrocyclic structure brings long fluorescence lifetime emission without fluorescence quenching and TD-DFT calculations revealed π–π interactions between the naphthalene rings.


2021 ◽  
Author(s):  
Verena Wulf ◽  
Gadi Slor ◽  
Parul Rathee ◽  
Roey J. Amir ◽  
Gili Bisker

Single-walled carbon nanotubes (SWCNTs), non-covalently functionalized by synthetic polymers, find widespread applications including sensing and imaging. Identifying new amphiphiles with interchangeable building blocks that can form unique coronae around the SWCNT, customized for a specific application, is thus of great interest. We present polymer-dendron hybrids, composed of hydrophobic dendrons and hydrophilic polyethylene glycol (PEG), as amphiphilic macromolecules with high degree of structural freedom, for suspending SWCNTs in aqeous solution. Based on a set of four PEG-dendrons differing in their dendritic end-groups, we show thst differences in the chemical structure of the hydrophobic end-groups control the interactions of the PEG-dendrons with the SWCNT-surface. These interactions led to differences in the intrinsic near-infrared fluorescence emission of the SWCNTs and affected the PEG-dendron susceptibility to enzymatic degradation, which was monitored by the SWCNT fluorescent signal. Our findings open new avenues for rational design of SWCNT functionalization, and optical sensing of enzymatic activity<br>


2021 ◽  
Author(s):  
Verena Wulf ◽  
Gadi Slor ◽  
Parul Rathee ◽  
Roey J. Amir ◽  
Gili Bisker

Single-walled carbon nanotubes (SWCNTs), non-covalently functionalized by synthetic polymers, find widespread applications including sensing and imaging. Identifying new amphiphiles with interchangeable building blocks that can form unique coronae around the SWCNT, customized for a specific application, is thus of great interest. We present polymer-dendron hybrids, composed of hydrophobic dendrons and hydrophilic polyethylene glycol (PEG), as amphiphilic macromolecules with high degree of structural freedom, for suspending SWCNTs in aqeous solution. Based on a set of four PEG-dendrons differing in their dendritic end-groups, we show thst differences in the chemical structure of the hydrophobic end-groups control the interactions of the PEG-dendrons with the SWCNT-surface. These interactions led to differences in the intrinsic near-infrared fluorescence emission of the SWCNTs and affected the PEG-dendron susceptibility to enzymatic degradation, which was monitored by the SWCNT fluorescent signal. Our findings open new avenues for rational design of SWCNT functionalization, and optical sensing of enzymatic activity<br>


PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0243218
Author(s):  
Tracy Matray ◽  
Sharat Singh ◽  
Hesham Sherif ◽  
Kenneth Farber ◽  
Erin Kwang ◽  
...  

In the pursuit of a novel class of fluorescent dyes we have developed a programmable polymer system that enables the rational design and control of macromolecular constructs through simple control of polymer primary sequence. These polymers are assembled using standard phosphoramidite chemistry on a DNA synthesizer which allows for extremely rapid prototyping and enables many permutations due to the large selection of phosphoramidite monomers presently available on the market. This programmability to some extent allows us to control the interactions/spacing of payload molecules distributed along the designed polymeric backbone. Control of molecular architecture using this technology has allowed us to address the long-standing technical issue of contact quenching between fluorescent dyes offering new possibilities in the life sciences arena. Much like peptidic sequences coding for enzymes, cofactors, and receptors (all needing control of tertiary structure for proper function via primary sequence) our programmable system approaches a similar endpoint using a phosphate based polymeric backbone assembled in a completely automated fashion. Using this novel technology, we have efficiently synthesized several types of fluorescent dyes and demonstrated the programmability in molecule design, including the increases in brightness of the fluorescence emission.


2021 ◽  
Vol 23 (1) ◽  
pp. 219-228
Author(s):  
Nabanita Saikia ◽  
Mohamed Taha ◽  
Ravindra Pandey

The rational design of self-assembled nanobio-molecular hybrids of peptide nucleic acids with single-wall nanotubes rely on understanding how biomolecules recognize and mediate intermolecular interactions with the nanomaterial's surface.


2020 ◽  
Vol 8 (35) ◽  
pp. 18207-18214
Author(s):  
Dongbo Jia ◽  
Lili Han ◽  
Ying Li ◽  
Wenjun He ◽  
Caichi Liu ◽  
...  

A novel, rational design for porous S-vacancy nickel sulfide catalysts with remarkable catalytic performance for alkaline HER.


Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
ES Halldorsdottir ◽  
S Oddsson ◽  
AM Einarsdottir ◽  
B Eiriksdottir ◽  
NM Kowal ◽  
...  

1993 ◽  
Vol 69 (02) ◽  
pp. 157-163 ◽  
Author(s):  
Irving Fox ◽  
Adrian Dawson ◽  
Peter Loynds ◽  
Jane Eisner ◽  
Kathleen Findlen ◽  
...  

SummaryHirulog™ (BG8967) is a direct thrombin inhibitor built by rational design using the protein hirudin as a model (Maraganore et al. [1990]; Biochemistry 29: 7095–101). In order to evaluate the therapeutic potential for hirulog in the management of thrombotic disease, the tolerability and anticoagulant activity of the agent were examined in a study of human volunteers.In a randomized, placebo-controlled study (n = 54), the intravenous infusion of hirulog over 15 min showed a rapid, dose-dependent prolongation of activated partial thromboplastin time (APTT), prothrombin time (PT), and thrombin time (TT). There was a corresponding dose-dependent increase in plasma hirulog levels. The peptide was rapidly cleared with a half-life of 36 min and a total body clearance rate for the peptide of 0.43 1 kg−1 h−1. Similar activity was observed following subcutaneous injection but with sustained pharmacodynamic and pharmacokinetic behavior. There was a significant correlation between pharmacokinetic and pharmacodynamic variables for both intravenous (r = 0.8, p <0.001) and subcutaneous administration (r = 0.7, p = 0.002).To evaluate the possible interactions of aspirin on the tolerability and anticoagulant activity of intravenous hirulog, a cross-over design was employed in eight subjects. Aspirin administration did not modify the peptide’s activity. At the administered dose of 0.6 mg kg−1 h−1 for 2 h, hirulog infusion prolonged APTT from 230 to 260% baseline. The infusion of hirulog in subjects who had received aspirin was not associated with any significant changes in the template bleeding time.The final phase of the study examined the activity and tolerability of hirulog in ten subjects during prolonged intravenous infusions for up to 24 h. The peptide (0.3 mg kg−1 h−1) exhibited sustained anticoagulant activity with no evidence for a cumulative effect. During hirulog infusion, APTT was prolonged from 210 to 250% baseline.In all phases of the study, hirulog administration was generally well-tolerated.Our observations show that hirulog is an active antithrombin agent with excellent tolerability in humans. As a direct thrombin inhibitor, hirulog provides a novel approach for the management of thrombotic disease.


Sign in / Sign up

Export Citation Format

Share Document