13th biennial conference of Infrared & Raman User Group, shortly IRUG, was for the first time ever held in Sydney, Australia in a beautiful Art Gallery of New South Wales. IRUG conferences are gathering people using IR and Raman spectroscopy for the analysis of cultural heritage, architecture, and forensic materials. This year 101 people were attending, including Dr Signe Vahur and PhD student Pilleriin Peets from our group. Pilleriin was also introducing her results in analyzing textile fibres with IR spectroscopy in an oral presentation. Development of methods for the analysis of various textiles using ATR- and reflectance FT-IR spectroscopy turned out to be very relevant: throughout all three days, many people approached to discuss the topic, ask questions and advice or to make contacts for later cooperation. We were also very glad that conference participants were interested in our ATR-FT-IR spectral database of cultural heritage and conservation materials, available here.
Three days were filled with a wide range of interesting presentations from analysis of Aboriginal Australian pigments and identification of contents from the coffin of a 2500-year-old Egyptian mummy Mer-Neith-it-es to investigations of cultural heritage materials using neutron techniques. Besides the analysis of traditional pigments, organic pigments, especially synthetic organic pigments and their use in art were discussed (oral presentation by Dr Suzanne Lomax and Dr Steven Saverwyns). Another very interesting and thought-provoking presentation was done by Dr Gregory Smith from Indianapolis Museum of Art. He discussed the difficulties in getting accurate standard reference materials in the field of cultural heritage analysis. His results showing how many false materials can be found on the market (and not only vendors like Kremer Pigmente, but also providers like Sigma Aldrich) were very surprising.
All in all, IRUG 13 conference offered three full days of interesting presentations, a lot of knowledge and useful tips for further research and a pleasant atmosphere with excellent company.
Main concern while measuring ionization efficiency (IE) of derivatized compounds is that derivatized compounds are in complex mixtures. To overcome this problem, we developed a chromatographic method to separate these compounds and measure their ionization efficiencies.
If ionization efficiencies of derivatized compounds are measured without chromatographic separation in a complex mixture, which includes analytes, derivatization reagents and different by-products, then matrix effects could occur. This problem can be solved if we first separate these compounds from each other and then measure ionization efficiencies.
Chromatographic method
To separate different compounds, we used a simple chromatographic gradient elution method. One might think, that if compounds have different retention time, then they also elute at different organic phase percentages which obviously affects measured ionization efficiency values. The effect is not so significant, but we could manage to model it and take it into account to level all newly measured ionization efficiency values to a previously measured scale.
logIE measurements
We carried out ionization efficiency measurements with liquid chromatography electrospray ionization mass spectrometry (LC/ESI/MS) and constructed IE scales with a calibration curve for compounds with and without derivatization reagent diethyl ethoxymethylenemalonate (DEEMM). Additionally, we investigated eluent composition effects on ionization. Measured compounds were mainly amino acids but also included some biogenic amines.
Results
We saw, that
Derivatization increases IE for most of the compounds (by an average of 0.9 and up to 2 – 2.5 logIE units) and derivatized compounds have more similar logIE values than their underivatized variants.
Measurement of derivatized compounds is possible from the mixture when using chromatographic separation technique.
It was also noted, that using chromatographic separation instead of flow injection mode tends to slightly increase ionization efficiency.
We managed to link all our results with existing ionization efficiency scale and therefore widen the scale and get comparable logIE values for measured derivatized compounds.
Dr. Anneli Kruve defended her PhD thesis – “Matrix effects in liquid-chromatography electrospray mass-spectrometry” in University of Tartu in 2011 under the supervision of prof. Ivo Leito and dr. Koit Herodes. Right after she got her first personal funding and established the electrospray ionization efficiency studies group. In addition to understanding the ionization mechanism for small molecules in electrospray, she is interested in using charged nanodroplets generated by electrospray as an organic synthesis medium. In 2016 Dr. Anneli Kruve moved to Haifa, Israel to do her first post-doc at the Technion’s Schulich Faculty of Chemistry in Prof. Israel Schechter’s group. Right now, she is a Humboldt Fellow in the Institute of Chemistry and Biochemistry at Freie Universität Berlin in Germany in Prof. Christoph Schalley’s group.
In addition to excellent science, she is spreading the knowledge as she has designed and is actively lecturing different courses (instrumental analysis lab, statistics in analytical chemistry to name some) in analytical chemistry and statistics in analytical chemistry. She has also supervised several PhD and numerous MSc and BSc students.
Early inspiration
“I got started in organic synthesis but quickly joined a biomedical lab that needed students to operate a HPLC. From there, moving to LC/MS was a natural step. The ability to incorporate various skills from IT to synthesis with mass spectrometry-based research has kept me motivated to stay on this path.”
Research
“My field is structural and quantitative characterization of compounds with LC/ESI/IMS/MS. A key focus of mine is developing the possibility of giving a quantitative context to non-target LC/HRMS data without the need for standard substances.”
Greatest achievement
“I have already seen many students moving from our lab to the workforce and receiving positive feedback from their employers – that definitely makes a former supervisor happy!”
Prediction
“Mass spectrometry has already changed almost everything; its impact will increase further, as we make non-target screening more efficient with effective algorithms, and make it quantitative. I also have a dream technique: I sometimes wonder what the world would look like with MS-(gas phase)NMR . . .” (The Analytical Scientist)
We are very happy and proud that Dr. Anneli Kruve received this well-deservedly recognition of being nominated to the Top 40 Under 40 Power List by the Analytical Scientist!
From 26 to 31 of August Florence hosted a vast majority of mass spectrometry scientist in the course of 22nd International Mass Spectrometry Conference. Among these were also our group members researchers Anneli Kruve and Riin Rebane, PhD students Piia Liigand and Jaanus Liigand, MSc student Mari Ojakivi and a visiting PhD student Tingting Wang from the Technical University of Denmark. We had a chance to present altogether 5 posters at the conference. Our posters can be found here. As is the case for IMSC, the topics ranged as wide as it can be for mass spec and always there was something to see and hear. We were happy to see that there was a lot of interest in our work. Congratulations to Anneli, whose poster received Chemistry – A European journal poster award! The conference was accompanied by delicious Italian food and nice warm weather. We enjoyed every second of this highly intensive week and are looking forward to IMSC 2020 in Rio.
Anneli Kruve: It is no secret that I am very keen on non-target screening methods, so I really enjoyed all the talks and posters regarding non-target screening and compound identification. My favorite talk was actually also in the field of compound identification given by Prof. Rober Mistrik in the Thermo lunch seminar. He very nicely explained the Precursor Ion Fingerprinting strategy and explained some of the new tips and tricks which are now combined in the Mass Frontier 8.0. It also very strongly resonated with the perspective I recently wrote about semi-quantitative non-target screening. I also have to mention the plenary lecture by Prof. Marco Leona from Metropolitan Museum of Art, who did not focus specifically on mass spec but gave us a really nice overview of scientific research of art. I constantly kept thinking how beautiful it is to have a background in chemistry: one can, virtually, combine all interest and make a great new whole. Prof. Leona, for example, was combining beautiful artworks, history of humankind, the biology of colorful bugs and plants, and on top of that mass spectrometry. And I definitely also felt honored to receive my best poster prize awarded by Chemistry – A European Journal!
Riin Rebane: It was my first experience of Florence as well as IMSC and when the first one greeted with wonderful food, the second one gave food for thought. It was a thorough overview of the latest advances in mass spectrometry and an insight into different works of scientists from academia as well as industry, therefore, it was certainly a challenge to grasp it all. But despite that, it was also nice to see that sessions towards practical applications of mass spectrometry in for example food or environmental analysis, were so popular that arriving late meant that all seats were already taken by other enthusiasts.
Mari Ojakivi: IMSC 2018 was the first scientific conference that I attended and as a master’s student it was an eye-opening experience. It was very nice to see so many scientists introducing their brilliant work with a mass spec. Seeing all the different applications in forensics, food and environmental science, as well as fundamental research in all the -omics fields made me understand how powerful tool mass spectrometry is. What is more, presenting my own work and seeing other scientists being so interested in it, verified that I am doing good and important science.
Piia Liigand: I thoroughly enjoyed the IMSC 2018 in Florence. It was a nice opportunity to meet and talk to scientists from all over the world. I was also very positively surprised to see so much interest in my poster and I truly enjoyed the discussions I had while presenting my poster. Thanks to these discussions I now have even more understanding of the importance of the science we do and what to do next. I also enjoyed meeting friends from past conferences and catching up on their research in more detail. Of course, the food, wine and general ambiance of Florence was an excellent environment to do all that.
Jaanus Liigand: I enjoyed the IMSC 2018 in Florence as it offered a very wide set of different interesting topics of mass spectrometry field. The inspiring presentations, fruitful discussions, interdisciplinary ideas, and excellent community made it a very enjoyable conference. My favorite session was environmental MS where Prof. Susan Richardson gave in her keynote a very nice overview of the recent developments in this field followed by interesting presentations. Additionally, I enjoyed meeting friends from previous conferences and discussing their and our research. Of course, the historical city – Florence – with the food and wine scenery made the week even more enjoyable.
Tingting Wang: It was a really memorable experience to participate IMSC in Florence, and I enjoyed the atmosphere and all the academic events there. It’s so impressive how wide are the application fields that mass spectrometry can do in the world by looking through a thousand posters. It’s hard to say which presentation or poster was my favorite, but I do pay more attention to the non-target screening strategy applied in food control, environmental, metabolomics, and proteomics study, especially the workshop on the second day about non-target analysis. It was interesting and very informative because unknown screening by high-resolution mass spectrometry is the topic of my PhD project, how to combine target and non-target screening, how to develop a more precise identification and quantification strategy for the non-target even unknowns, and how to prioritize unknowns are the problems I am always facing. It is nice that I could see these similar studies with various workflows from other researchers, and have the chance to listen to their presentations and even talk with those people to get inspiration for my research.
Anneli, Riin, Mari, Jaanus and Piia presenting their posters.
On the 20th -23rd of August 2018 Eliise, Pilleriin and Markus, who regularly use the FT-ICR-MS as part of their research, attended the first EU FT-ICR MS End User School. The school was organized by professor Janne Jänis and took place in the University of Eastern Finland in Joensuu. The school is part of the efforts of the European Network of Fourier Transform Ion Cyclotron Resonance Mass Spectrometry Centres (www.eu-fticr-ms.eu, the materials and slides from the course will also be available on this website under the documents section in the near future) to establish an EU community of end-users and FT-ICR-MS scientists. The objective of this network is to promote and provide resources for the wider application of FT-ICR-MS instruments by European academic, industrial and business institutions. The school was intended for researchers and students who are still relatively new to the machine.
The school consisted mostly of lectures by some of the world’s leading experts on FT-ICR MS. A few examples include prof. Peter O’Connor covering the fundamentals of FT-ICR-MS along with sharing some guidelines to follow in order to get the most out of one’s ICR and Evgeny Nikolaev talking about the dynamically harmonized ICR cell which he invented. In general, many different topics were covered: data acquisition and signal processing, isotopic fine structure and quadrupolar detection, atmospheric pressure ion sources, various applications of the machine etc.
Every day after the lectures some time was given for the attendees to present short talks covering their own research. The students also had the opportunity to present posters which could be viewed during the breaks between lectures. There was a 200€ prize for the best poster which was won by Anika Neuman for her work concerning the comparison of APCI and photoionization for gas analysis with FT-ICR-MS.
On the 21st of August the organizers gave a short tour of the universities FT-ICR-MS lab where they showed their 12 Tesla Bruker APEX-Qe instrument.
The summer school also included a half-day trip to the nearby Valamo monastery and whiskey distillery where a short excursion was accompanied with a wine tasting session and lunch.
All in all the summer school proved to be very beneficial to the attendees as along with gathering several new ideas regarding the most efficient use of the machine, many contacts were established with experts in the field.
This week two PhD students of our group, Rūta Veigure and Max Hecht had a chance to present their research in the 7th European Association for Chemical and Molecular Sciences (EuCheMS) Congress in Liverpool, organized by the European chemistry society. The conference offered a 5 day packed programme and celebrated the organization of different chemists in societies all over the world. For example, the Estonian chemical society is turning 100 years this year.
Rūta Veigure presented a poster on “Widening the range of eluent additives for LC-MS analysis to improve the retention of drug-like molecules”, while Max Hecht delivered a talk on the “The Evolution of Sponge spray for direct Sampling and Analysis by MS”.
Liverpool itself offered a variety of sights and enjoyable experiences, and as being the home-town of Beatles, there was even a chance to enjoy the tribute band “The Bootleg Beatles” during one of the Congress’ evenings.
The logIE approach is already applicable in nice clean matrices such as neat solvents. We wanted to see if our approach also works with more difficult matrices, such as bodily fluids and tissues. The results were recently published in Analytica Chimica Acta.
In this study, we took a representative set of 10 compounds, including drugs, e.g., naproxen and lincomycin. As matrices, we used blood, plasma, urine, cerebrospinal fluid, brain and liver tissue homogenates and neat solvent to compare with. We carried out a simple and robust sample pretreatment of protein precipitation. We measured the IEs in a worst-case scenario in flow injection mode without any chromatographic separation.
As with different instrumental setups and solvents, the IEs vary between biological matrices, but the order of the compounds remains roughly the same. These variations between different matrices and variations between a certain biological matrix and neat solvent demonstrate that matrix affects ionization efficiencies and also the prediction models of ionization efficiencies. This, in turn, shows that matrix affects the importance of properties of compounds in the prediction model.
Even though the effects are big and matrix effect is strong we were happy to see that the correlations between IEs measured in the neat solvent and IEs measured in a biological matrix are in good correlation (R2 from 0.7 to 0.9). These good correlations were a promising start to predict IEs in biological matrices similarly to previous predictions in the neat solvent. The most accurate model was obtained for the solvent with a mismatch of 2 times which was also expected since it is the cleanest matrix. But also for liver and brain tissues the mismatch of the model is only 3-fold.
The correlation between predicted and calculated IEs is good with the average mismatch over all biological matrices of 8 times. This means that the accuracy of standard substance free quantitation has been improved by more than an order of magnitude for the set of compounds used in this study.
More details can be found in the paper published in Analytica Chimica Acta. Piia Liigand also gave a talk on the topic in ASMS which can be found here. More papers by our group on the topic of ionization efficiencies can be found here.
We demonstrated the fruitfulness of multiproxy dietary analysis combining plant microfossil, human bone stable isotope and pottery related organic residue analysis. The results reveal that even 800 years ago men and women had different dietary habits: men preferred fish and higher trophic level terrestrial animals (e.g. pork), whilst women declined towards ruminant carcass (a nice steak!) and dairy products.
The paper is one of the few of its kind illustrating ancient food consumption as a highly social phenomenon, and setting an example for microscale dietary analysis in the future.
Traditionally, in the first half of June, our bachelor and master students defend their theses. This year there were 3 masters students and 2 bachelor students from our group. Here is how the students described their theses.
Alo Rüütel “Synthesis of bambusuril macrocycles and investigation of their binding properties”, master’s defence In my master’s thesis, I synthesized bambusuril macrocycles. These receptor molecules are very potent anion binders. Usually, molecular receptors do not function in water because they are not able to bind target molecules with sufficient strength. Some bambusuril derivatives are able to function in aqueous media, which makes them a very special type of macrocyclic receptors. It is possible to use these molecules as ionophores for anion selective electrodes.
Ernesto de Jesus Zapata Flores “Determination of free diisocyanates in polyurethane foam”, master’s defence My thesis focused on the test of a proposed method to analyze free diisocyanates in polyurethane foams for two reasons, by one side those compounds can represent a danger if care is not taken when the foam is used, and by the other side, new legislation is more aggressive against those compounds. The method is a simpler alternative to achieve the derivatization of diisocyanates.
Andre Leesment “Gas phase acidity measurements of superacids using FT-ICR method”, master’s defence
My master’s thesis was based on gas-phase acidity measurements of some very strong acids. Such strong acids are widely used in organic synthesis as reactants and/or catalysts. The anions of such acids exhibit high stability, which makes the valuable components of contemporary energy storing devices. The obtained results allow us to work on expanding the self-consistent gas-phase acidity scale with acids stronger than the ones experimentally measured so far.
Lisett Kiudorv “Quantitative analysis of clay components using ATR-FT-IR spectroscopy”, bachelor’s defence The main purpose of my bachelor’s thesis was to develop a method that enables quantitative analysis of clays using ATR-FT-IR spectroscopy combined with the chemometric partial least squares method. The developed method is quick and easy to use and reduces the required sample size to around a milligram. The dramatic decrease in sample size makes it possible to analyse samples from archaeology and art. The method was then used to analyse six archaeological samples including one of the oldest potteries found in Estonia and an Egyptian pottery, which holds a bird’s mummy.
Elisabeth Parman “Determination of pKa values of fluorocompounds in water using 19F NMR”, bachelor’s defence The main aim of my bachelor’s thesis was to determine pKa values of fluorocompounds in water using 19F NMR. This method is not particularly commonly used, but it can be used to verify or disconfirm values that have been measured with different methods, especially in cases where the measurements with other methods are problematic. For example, the purity and accurate concentration of the measured compound need to be concerned for most of the methods, but with 19F NMR it is not problematic.
Every year Estonian University of Life Sciences organises a conference called “Healthy animal and healthy food” where Dr. Riin Rebane made a presentation “Fight against food fraud” which explained the ever-expanding role of analytical chemists in food science. Reasons for food fraud vary, but are almost always for monetary gain and therefore food fraud is in constant progress. One good example is honey analysis, where for decades there has been a change in methods in order to identify whether honey is real or whether it is identified with correct botanical or geographical origin. As a natural product, no two honeys are identical and this makes identification further more challenging for the chemists. One of the possible methods is amino acid analysis since the amino acid content can be like a fingerprint for honeys and in University of Tartu we have analysed few hundreds of Estonian honeys and have seen that that foreign honeys do differ in most cases and also that there is a correlation between the amino acid content and botanical origin. But nevertheless, even this method might not work every time and chemists are looking towards methods such as nuclear magnetic resonance spectroscopy and even DNA-analysis to get better certainty for determining the origin of honey.
The summary based on the presentation was also reported in the newspaper Maaleht.
