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FNR ATTRACT Fellows – the people behind the science: César Pascual García

 

BACK TO RESEARCH WITH IMPACT: FNR HIGHLIGHTS

What is your background?

“I was born and raised in Madrid. When it came to choosing a subject to study at University, I chose physics, because I was good at it in school. After completing my Masters in Madrid, I spent around seven years in Pisa, Italy, where I did my PhD in Solid State Physics and a Postdoc working with Nano devices with metal-superconductor interfaces, before I started working as a Scientific Officer at the European Commission’s Institute for Health and Consumer Protection in Italy.”

What did your role as a Scientific Officer at the European Commission (EC) entail?

“My main responsibility was to provide scientific answers to the EC on aspects related to European policy linked to nanotechnology, such as developing characterisation methods for industry or assessing toxicology. I for example developed new approaches to analyse nanomaterials and study their interactions, and set up the current facilities of electron transmission microscopy and electron and ion scanning microscopy.”

Why did you decide to leave your permanent position at the EC to come to Luxembourg and return to research?

“On one side, it was of interest to me because my wife was already living in Luxembourg, and we were expecting our first child. However, it was also out of professional interest. In the EU Commission, my job was limited, but I had many ideas for things I wanted to develop. I had an idea about how to apply some techniques that are applied to semiconductor technology to chemistry: what if we could have billions of chemical connections happening at the same time using nanotechnology?

“I came to LIST (CRP Gabriel Lippmann at the time) and I presented my project idea. That was the first step. I saw this opportunity to develop the project here in Luxembourg and the FNR ATTRACT Fellowship made it possible.”

For your ATTRACT project, you are combining nanotechnology with personalised medicine. Can you go into more detail?

“We create sensors using nanotechnology that can later be applied in personalised medicine. If what we are developing now works, we may be able to control biopolymers – this is the ambition. ATTRACT has helped us understand which biopolymers we will be able to control: proteins.

“In personalised medicine you have to take a sample from the patient – you have to understand and compare the cells of a healthy patient with those of a patient with a disease. We don’t yet understand the language of proteins – when we see a sequence of amino acids, we don’t know what they are going to do. We try to look at what is and what is not ok, spotting the differences. The issue here: there are billions of amino-acid sequences from the proteins to compare; therefore finding differences between them is a huge task.”

César with his team – left to right: Serena Rollo (PhD); César Pascual García; Dipti Rani (Postdoc); Divya Balakrishnan (PhD). “Everyone has a different style of PhD supervising: Mine involves talking a lot – I think the research we do works better when it is shared. Our team has meetings every week; this also helps us review the areas where we could do better.”

How are you addressing this issue with your nanotechnology sensors?

“We are making sensors that are aiming to analyse samples coming from healthy and diseased cells. When you go to do a blood analysis, the doctor has a sheet with what they want to check – your cholesterol, antibodies etc. They know what they are looking at. In personalised medicine, by definition, you don’t have that. Instead, the information from your cells would analysed and they would give clues to what is wrong.”

“We create sensors using nanotechnology that can later be applied in personalised medicine. If what we are developing now works, we may be able to control biopolymers – this is the ambition.”

Looking at the big picture – do you see yourself following the sensor all the way to application, or is your focus more on the practical work of developing these types of sensors?

“I am good at some things – such as fabricating using nanotechnology – and not good at other things, for example running a company. I know that because I have seen what it takes. We need to continue advancing, then at the point where we have shown that our sensor works, we will hand it over to someone else.

“I will be happy if it is successful, but I am not interested in the business side of the device. Once it works, we will start something new. I see myself creating a device, perfecting it, then handing it over to be implemented. The goal is always to release something physical so someone else can work with it.”

So your focus is on manufacturing a device that can directly be used to innovate medicine, rather than testing theories in the lab.

“There is theory behind it – such as modelling the sensor and understanding the processes that made it work. But yes – at the end there has to be something physical, a device. People have to see that it works in practice. That is something I like a lot – to fabricate something, see how it works, and fine tune the properties. It’s fun – it’s a bit like having a device made of Lego with motors and switches.”

“I think the facilities we work with at LIST are state of the art now. Plus, many of the machines we use are flexible and can be used for several purposes, by different teams.” Cesar here shown with the evaporator, which heats up and evaporates metal before depositing it on a surface.

What are your thoughts on how fast diagnostics and nanotechnology in health are evolving?

“Time is extremely important in my project, we do not have time for many errors. In molecular diagnostics, there have been huge advances in the last years. We entered the genetic era very fast and now you can easily get a genetic analysis.

“When I came to Luxembourg in 2014, my wife and I had our first child and we did not consider a genetic test. We knew they exist, but they were expensive. Our second child came 18 months later. At the beginning of the pregnancy, the doctors were considering a genetic test, but it was still something that had to be done abroad. By the end of the pregnancy, this test was much more readily available and as a result the price had decreased significantly.

“I think we are the edge of a new era now: the proteomics era, which is all about the study of proteins on a large scale. There are still a lot of challenges, and we think we can contribute. We are at a position in time where what we are creating is needed, we have a market of applications.”

Did you experience any challenges getting started, seeing as your project was in a field somewhat new to you?

“Everything was new! During the first year, I was asking myself ‘can I do this?’, during the second year it switched to ‘it doesn’t matter, I have to do this’, and then by the third year everything started running a bit more smoothly.

“Getting fellow scientists to collaborate on the project was also tough, at first. When I started contacting the people who are now collaborating with us, it was always a surprise for them. I called and said as someone new in the field, I would like someone to look over my shoulder and tell me if I’m going in the right direction. The first of these conversations were not easy – but now we have strong collaborations with around 20 researchers, for example in the Netherlands and Denmark.”

Sensor in electron microscope, for example used to fabricate nanowire sensor devices

Your background is multidisciplinary; you have worked in several fields related to physics. What would you say is the common thread?

“Yes, I have developed skills in areas including Thin Films, Materials Science, Nanomaterials, Spectroscopy, and Scanning Electron Microscopy – but the common thread in my career is that I know how to fabricate things with nanotechnology. I think I’m a varied scientist – I don’t have one topic that I am following: I did my PhD on one topic, then I did a Postdoc on something very different and then I started my position at the European Commission, which again involved other topics. My ATTRACT, again, is on a different topic entirely. It has been a challenge, but I am very happy and I am pleased with where my decisions have led me.”

Where do you find inspiration?

“My main source of inspiration comes from talking to people, even though I am an introvert. I have very good friends, and I learn a lot from them. I also get along well with other researchers, such as Phil Dale and Stan Schymanski (also FNR ATTRACT Fellows) – we often meet, and enjoy talking. It’s beyond having a common project. We cross paths and try to have creative lunches together every once in a while. Luxembourg, due to its size, means you are naturally exposed to researchers in other fields. This brings opportunities you do not have in other countries.”


1995

Amazon is born

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1998

Amazon Prime debuts

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1998 – 2001

Amazon acquires Audible

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2001 – 2007

PhD student in Solid State Physics at SNS (Pisa, Italy)

2007 – 2009

Postdoc in field of Condensed Matter Physics at NEST-INFM (Pisa, Italy)

2009 – 2013

Scientific Officer, European Commission Institute for Health and Consumer Protection (Italy)

2014

Secures FNR ATTRACT Fellowship and moves to Luxembourg to embark on Project NANO-PH (Nano electronics for pH control and ultra-dense electrochemical synthesis) at CRP Gabriel Lippmann (now LIST – Luxembourg Institute of Science and Technology)

More in the series FNR ATTRACT FELLOWS: THE PEOPLE BEHIND THE SCIENCE