Author Archive

Potential route to a universal biosensing platform

A fully functional surface-tethered protein switch has been reported by US scientists. It is the first step towards a universal biosensor platform, they claim. 

Peter Searson, at John Hopkins University, Baltimore, and colleagues attached a protein switch with a maltose binding protein input domain and a beta-lactamase output domain to a gold surface. When maltose bound to the input domain, it switched on the beta-lactamase’s activity, which the team measured using the yellow-to-red colour change that took place as it hydrolysed the beta-lactam ring in nitrocefin.  Different input domains could be coupled to the same output domain, offering a potential route to a universal biosensing platform.

Read Surface-tethered protein switches, recently published as an Advance article in ChemComm.

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Approaching deadline for Emerging Investigator Lectureship nominations

Time is running out to nominate your colleagues for the ChemComm Emerging Investigator Lectureship 2011. Send your nominee’s details to the ChemComm Editorial Office by 28th February 2011.

And remember, to be eligible for the ChemComm Emerging Investigator Lectureship, the candidate should be within the first eight years of completing their PhD. Find out more….

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Congratulations to Jean-François Nierengarten

Jean-François NierengartenWhat’s special about Gene delivery with polycationic fullerene hexakis-adducts?

Well, that’s the topic of Jean-François Nierengarten’s recent ChemComm communication, rated as ‘hot’ by the referees and free to access* until 15th March. It is also his 25th independent research article in ChemComm.

To celebrate this achievement, Professor Nierengarten has taken some time out from his research to speak to ChemComm about his career.

What inspired you to become a scientist?
As far as I remember, I was always fascinated by natural sciences and wildlife. I started to study biology at the University of Strasbourg (Université Louis Pasteur at that time) with the idea of becoming a zoologist to discover unknown animals in the Amazon rainforest or in other wild places in the world. On the way, I discovered chemistry thanks to a couple of outstanding teachers and definitively switched from biology to chemistry after I met Jean-Pierre Sauvage at the end of my first year of Master. Fortunately, after my Master, I had the chance to prepare my PhD under the guidance of Jean-Pierre, and thus to become a chemist.

What was your motivation behind the work described in your ChemComm article?
The work described in this paper is a part of our research program on the use of click chemistry for the post-functionalisation of fullerene hexa-adducts (Chem. Commun. 2008, 2450; 2010, 46, 3860 and 4160; 2011, 47, 1321). The initial driving force for this work was to apply the synthetic methodology developed in the group to the preparation of new molecules with specific properties. As very often happens, applications with our compounds rely on collaborations with colleagues having the appropriate expertise. Indeed, Jean-Serge Remy, a well-established scientist in the field of transfection and synthetic vectors, is a very good friend and discussing about science one Friday evening in a pub brought us to the idea of testing fullerene hexa-adducts as synthetic vectors. We thus prepared a series of hexa-substituted fullerene derivatives decorated with dendritic branches bearing peripheral ammonium groups. Jean-Serge and his co-workers could then show that polyplexes prepared from DNA and these globular polycationic fullerene derivatives exhibit remarkable gene delivery capabilities. This result was quite unexpected as a generally admitted rule for the design of gene delivery vectors is that compact globular polycations with an isotropic distribution of positive charges are not suitable candidates for such studies. The results reported in our ChemComm article show that this is indeed not the case.

Why did you choose ChemComm to publish your work?
For fast publication of our important findings, ChemComm is an obvious choice. Over the years, it has been always a pleasure to work with the RSC Journals in general and with ChemComm in particular. All the steps from the submission to the publication are very efficient and all is organized in a very professional way. Publishing our work in ChemComm is also the guarantee for high visibility. Finally, I am a supporter of European journals in general and strongly believe that the best of European chemistry should be reported in European journals. Having top quality journals in Europe is essential to give credit to the European chemical community.

Where do you see your research heading next?
In addition to their remarkable gene delivery capabilities, the fullerene hexa-adduct derivatives have also revealed a very low toxicity if any. The fullerene hexa-adduct core is therefore a particularly appealing 3D-scaffold for the development of new multifunctional bioactive molecules. Based on the versatile fullerene hexa-adduct building blocks already developed in our group (Chem. Commun. 2010, 46, 4160), the successive grafting of up to three different groups on the fullerene core can be efficiently achieved. We are currently working on a new generation of vectors bearing targeting subunits for specific gene delivery to selected cells and/or fluorescent probes to monitor their intracellular pathway by confocal microscopy.

What do enjoy doing in your spare time?
Spending time with Iwona, my wife, and our two kids, cooking, listening to music, travelling. I like also reading and playing the guitar but have less and less time for it!

What would you be if you weren’t a scientist?
Hopefully as happy as I am to be a scientist! I guess that it could be the case if I would be an ébéniste [cabinet maker]. During my childhood, I had a lot of fun making stuff from wood in the workshop of my godfather, a very talented ébéniste particularly gifted for marquetry. I could spend hours watching him applying pieces of veneer to form decorative patterns or pictures onto the commodes or the tables he was restoring.

Also of interest:
Less is more – multiscale modelling of self-assembling multivalency and its impact on DNA binding and gene delivery
Paola Posocco, Sabrina Pricl, Simon Jones, Anna Barnard and David K. Smith
Chem. Sci., 2010, 1, 393-404

*Access our free content any time, any place – register for an RSC Publishing personal account today

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Announcing the ChemComm Emerging Investigators issue 2012

Following the success of the inaugural ChemComm Emerging Investigators issue, we are delighted to announce the forthcoming 2012 Emerging Investigators issue. All interested parties should contact the ChemComm Editorial Office in the first instance.

This issue is dedicated to profiling the very best research from scientists in the early stages of their independent careers from across the chemical sciences. We hope to feature principal investigators whose work has the potential to influence future directions in science or result in new and exciting developments.

 

Also of interest:
ChemComm Emerging Investigator Lectureship:
Submit your nominations by 28th February 2011

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Enzyme logic biosensor for security surveillance

Scientists in the US have made a system that rapidly detects both explosives and nerve agents, providing a simple yes-no response. The technique could replace two time-consuming tests that are currently used to assess these threats.

Joseph Wang and colleagues from the University of California, San Diego, combined their expertise in threat detection and electrochemical biosensors with the biocomputing experience of Evgeny Katz from Clarkson University, Potsdam, NY. The team produced an enzyme-based logic gate with the ability to simultaneously detect both nitroaromatic explosives and organophosphate nerve agents.

Graphical abstract: High-fidelity determination of security threats via a Boolean biocatalytic cascade

See Chemistry World for the full news story and download the ChemComm article to find out more.

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Sleeping Trojan horse to transport metal ions into cancer cells

UK researchers have used a cage-like molecule to smuggle metal ions into cells, which could improve medical imaging.

Medical imaging often requires getting unnatural materials such as metal ions into cells. Scientists have therefore had to come up with ways to disguise these compounds to get them past the cell membranes. Michael Coogan and colleagues at Cardiff University have come up with a way to avoid the current difficulties with some of these imaging treatments.

Graphical abstract: A ‘Sleeping Trojan Horse’ which transports metal ions into cells, localises in nucleoli, and has potential for bimodal fluorescence/PET imaging

Find out their solution by reading the news story in Chemistry World and downloading Coogan’s ChemComm communication.

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Palladium impurites are not essential for gold catalysis

Spanish scientists have proved that gold alone can catalyse cross-coupling reactions, following a claim made last year that palladium impurities in the gold are essential for the catalysis. 

Avelino Corma from the Polytechnic University of Valencia and colleagues used kinetic and theoretical studies to prove that gold can catalyse the Sonogashira coupling reaction between phenylacetylene and iodobenzene. ‘Gold nanoparticles are active enough to promote the reaction, regardless of the presence or absence of palladium,’ says Corma.

Graphical abstract: Gold catalyzes the Sonogashira coupling reaction without the requirement of palladium impurities

Read the full news story in Chemistry World and download Corma’s ChemComm communication

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Cram Lehn Pedersen Prize – winner announced

Congratulations to Professor Amar Flood (Indiana University) who is the winner of the Cram Lehn Pedersen prize 2011.

The prize, sponsored by ChemComm and named in honour of the winners of the 1987 Nobel Prize in Chemistry, recognises significant, original and independent work in supramolecular chemistry by emerging investigators.

The prize is awarded to Professor Flood for his pioneering work in macrocyclic and supramolecular chemistry and, in particular, for his development of receptors that employ pure CH hydrogen bonding to bind anionic guest species.

Professor Flood will receive £2,000 and will present his award lecture at the 6th International Symposium on Macrocyclic and Supramolecular Chemistry (6-ISMSC) in Brighton in July. ChemComm Editor Robert Eagling and Deputy Editor Joanne Thomson will be at the symposium – let us know if you’ll be there too.

Prof Phil Gale, Chair of the Scientific Committee for 6-ISMSC said: “I’m really delighted that Amar has been selected by the International Committee to be the first recipient of the Cram Lehn Pedersen Prize. I’m already looking forward to hearing his latest results in Brighton in July.”

Nominations for the 2012 award, which will be presented at 7-ISMSC in New Zealand, will open shortly. Email us to register your interest.

Find out more about Professor Flood’s research by reading his Chem Soc Rev tutorial review:

Click chemistry generates privileged CH hydrogen-bonding triazoles: the latest addition to anion supramolecular chemistry,  Yuran Hua and Amar H. Flood, Chem. Soc. Rev., 2010, 39, 1262-1271
(This review is part of the themed issue Click chemistry: Function follows form)

Also of interest:
A tristable [2]pseudo[2]rotaxane,  Ali Trabolsi, Albert C. Fahrenbach, Sanjeev K. Dey, Andrew I. Share, Douglas C. Friedman, Subhadeep Basu, Travis B. Gasa, Niveen M. Khashab, Sourav Saha, Ivan Aprahamian, Hussam A. Khatib, Amar H. Flood and J. Fraser Stoddart, Chem. Commun., 2010, 46, 871-873

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Novel concept for switchable olefin metathesis catalysts

Chemists have discovered a novel triggering mechanism for olefin metathesis catalysts while unravelling the mechanism of a crucial ligand rearrangement step.

Olefin metathesis is a widely used reaction in organic and polymer synthesis. cis Dichloro ruthenium benzylidene complexes bearing an N-heterocyclic carbene ligand have recently gained considerable attention as stable metathesis catalysts. They are known as latent catalysts as they initiate slowly, which is thought to be because the cis dichloro precursors have to rearrange to their trans dichloro counterparts to become active.

While studying the reaction mechanism, Christian Slugovc and colleagues at Graz University of Technology, Austria, discovered that a cationic complex is an intermediate in the rearrangement step. They also observed that pyridine, which is a donor ligand, facilitates the displacement of one of the chloride ligands, the first step in the rearrangement.

Graphical abstract: Pyridine as trigger for chloride isomerisation in chelated ruthenium benzylidene complexes: implications for olefin metathesis

But most striking, says Slugovc, is that the chloride counterion (or, more generally, a counterion that can coordinate to ruthenium) is indispensible for the catalytic activity. Changing the counterion for the non-coordinating hexafluorophosphate ion produced an almost inactive catalyst, but the activity was triggered again by adding chloride. Slugovc says this constitutes a novel concept for switchable olefin metathesis catalysts.

Download Slugovc’s ChemComm communication to find out more.

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Meet our author….Xin-Yan Wu

Xin-Yan Wu is an organic chemist based at East China University of Science and Technology, Shanghai, China. Her research focuses on the development of bifunctional organocatalysts, the subject of her recent ChemComm communication: Enantioselective intramolecular Rauhut–Currier reaction catalyzed by chiral phosphinothiourea

Find out more by downloading the communication – it is free to download until 14th February 2011.

Xin-Yan Wu has been talking to ChemComm about her work.

What inspired you to become a scientist?
I was fascinated with chemistry during high school and being a chemist became my dream. Therefore I chose chemistry as my major at university. During my undergraduate study I was greatly enchanted by the creativity and diversity of organic chemistry thus I chose to further pursue a doctorate in this field. After being awarded my PhD title, I joined Professor Qi-Lin Zhou’s research group (East China University of Science and Technology) and began to work in the field of asymmetric catalysis. My patient and silent nature was the catalyst for promoting me as a scientist.

What was the motivation behind the work described in your ChemComm article?
The development of new bifunctional organocatalysts became my research interest when I started to independently progress my research work. Although amino acid-derived aminophosphine compounds are useful intermediates for chiral ligands, they had never been used in asymmetric organocatalysis. In recent years we have developed phosphinothiourea derivatives as efficient catalysts. Initially, we focused on the Morita-Baylis-Hillman reaction and the 1,3-diploar cycloaddition. During the preparation of ω-formyl-enones as substrates for intramolecular Morita-Baylis-Hillman reaction via Wittig reaction, bis(enones) were obtained as by-products. We consequently envisioned whether chiral phosphinothiourea could catalyse the enantioselective Rauhut-Currier reaction of bis(enones). To the best of our knowledge, this reaction has scarcely been studied and the use of chiral organophosphine as its catalyst has never been reported. Hence, we attempted the phosphinothiourea as the catalyst for promoting such reaction, and fortunately we have obtained satisfactory results. Indeed, there are sometimes unexpected but pleasant surprises in research.

Why did you choose ChemComm to publish your work?
Because ChemComm is one of the most highly regarded international journals in chemistry and it possesses a broad readership.

Where do you see your research heading next?
We are now working on the enantioselective cycloaddition reactions catalysed by the amino acid-derived aminophosphines reported in the present paper. Meanwhile, we are seeking for other novel bifunctional organophosphines as organocatalysts, efficiently fulfilling a wide spectrum of enantioselective reactions.

What do you enjoy doing in your spare time?
I like cooking for my husband and writing blogs for my daughter.

If you could not be a scientist but could be anything else what would you be?
I would like to be a writer or a doctor.

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