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Perspective

Cite This: J. Chem. Inf. Model. XXXX, XXX, XXX−XXX pubs.acs.org/jcim

From Brazil to Germany: Challenges and Advantages


Ariane Nunes-Alves*,†,‡

Heidelberg Institute for Theoretical Studies (HITS), Schloß-Wolfsbrunnenweg 35, 69118 Heidelberg, Germany

Zentrum für Molekulare Biologie der Universität Heidelberg (ZMBH), Im Neuenheimer Feld 282, 69120 Heidelberg, Germany

ABSTRACT: Moving to a new country, with a different


culture and a new environment, is not an easy decision. In this
perspective, I present some reasons that made me, a Brazilian
computational biochemist, move abroad to do postdoctoral
See https://pubs.acs.org/sharingguidelines for options on how to legitimately share published articles.

research and some of the challenges I faced before and after


moving.
Downloaded via UNIV OF NEW ENGLAND on October 22, 2019 at 20:55:47 (UTC).

A fter a fruitful period of learning computational bio-


chemistry and publishing, I finished my Ph.D. at the end
of 2017 and exchanged the Brazilian summer for the German
colleagues on the postdoctoral path were stressed about not
having a stable job and the uncertainty of getting a position as
a principal investigator (PI) in the future. People who had left
winter. Why would someone exchange beautiful sunny days in academia missed the freedom of thinking and defining goals,
Brazil for cold and cloudy days in Germany? You will see I had but they were happy with a regular work schedule and a stable
good reasons for this. job.
I was born and raised in São Paulo, Brazil. When I was in A career as a PI looked like a good fit to me. Although I did
high school, there were many stories about the sequencing of not like the lack of stability of the temporary postdoctoral
the human genome and how this information had the potential positions one needs to get there, I enjoyed teaching and
to cure diseases. Such news inspired me to pursue a bachelor’s problem solving. It was fulfilling to think that, as a scientist, I
degree in biology at the University of São Paulo. In the end, I was adding a tiny little drop to the huge ocean of knowledge.
did not enjoy genetics very much, but I was fascinated by Therefore, I decided to do postdoctoral research to publish
biochemistry and also started working with Linux and C more papers and get more experience in teaching and advising
programming. This led me to do a Master’s degree and a Ph.D. students.
in biochemistry at the same university, working with The second crossroads was to decide where to do
computational methods under the supervision of Prof. Dr. postdoctoral research. Many reasons led me to do postdoctoral
Guilherme Menegon Arantes. During my Ph.D. studies, I was research abroad. The first was that this would allow me to gain
also a visiting researcher at the University of Pittsburgh, under a further understanding of my main area of interest, binding
the supervision of Prof. Dr. Daniel Zuckerman. During my kinetics. This topic was getting a lot of attention in the final
Master’s degree and Ph.D. studies, I developed methods for years of my Ph.D. studies due to the increasing evidence of the
predicting binding affinities using protein ensembles1 and for relationship between drug residence time, the time a drug
studying forced protein unfolding coupled to bond dissocia- spends bound to a protein, and in vivo efficacy.11,12 Another
tion.2 I also studied pathways for ligand unbinding from T4 reason was that a research stay abroad is valued by hiring
lysozyme.3 This last work drew my attention to ligand−protein committees in Brazil and would be a good opportunity to
binding kinetics, which has been my major research interest so increase my professional network, learn new computational
far. methods, and see things from a different perspective.
During my time as a graduate student, I saw interesting work Moreover, my experience as a visiting researcher in the United
in computational chemistry being developed in Brazil,4 like the States during my Ph.D. studies showed me that I was able to
free docking tool DockThor,5,6 methods for accelerated adapt to a life abroad.
quantum chemistry calculations using GPUs,7 and for My plan was to apply for positions in the United States and
simulating DNA oligonucleotides using adaptive resolution.8 Europe, where there are usually better funding resources for
The first crossroads of my transition happened in the final research. I anticipated that one of the major challenges would
years of my Ph.D. studies, when I started thinking about the be the interviews for landing a position. I knew flight costs for
next steps of my career. I talked to former graduate colleagues
about the possibilities. Most of them had moved on to
Special Issue: Molecular Simulation in Latin America: Coming of
postdoctoral research in Brazil or abroad, some of them went
Age
to the pharmaceutical industry to work as science liaisons or
researchers,9,10 and some became elementary or high-school Received: September 10, 2019
teachers in science or science-related disciplines. Often times

© XXXX American Chemical Society A DOI: 10.1021/acs.jcim.9b00764


J. Chem. Inf. Model. XXXX, XXX, XXX−XXX
Journal of Chemical Information and Modeling Perspective

an in-person interview would be expensive and that most to experience different cultures. Moreover, my laboratory is
interviews would happen by video conference. Since human very multicultural, with people from different parts of the
interactions through video conferences are very limited, I world, which has increased my cultural sensitivity.
feared it might be hard for a PI to decide whether I would be a My final advice to make one’s experience abroad smooth is
good fit for her or his group. Moreover, it would also be hard to choose the PI for your postdoctoral research or Ph.D.
for me to decide whether the laboratory environment would be studies carefully. Do you need someone who will micromanage
a good match for me. your tasks or someone who will give you time and space to
I made a list of laboratories to which I was going to apply for work on your own ideas? Do you feel comfortable in asking for
a postdoctoral position and planned to go to a couple of help, not only in professional, but also personal matters, like
international scientific meetings in the last two years of my visa problems? And after you get your position, I repeat the
Ph.D. studies to meet the PIs of these laboratories. This would advice from a previous perspective:9 ask questions and learn
alleviate the problem with video conference interviews. I tried from your colleagues. Computational chemistry is a multi-
to meet not only the PIs but also current or former Ph.D. disciplinary area of research, and research groups usually have
students and postdoctoral researchers to get a better idea of people with different backgrounds like biology, chemistry, or
the PI’s working style and laboratory environment. Talking to physics. Do not feel badly if you do not know something; the
graduate students was surprisingly useful. No one spoke fact is that no one knows everything.
negatively about her or his own laboratory, but sometimes
their body language while replying to my questions made it
very clear that some places were not so friendly. Another piece
■ AUTHOR INFORMATION
Corresponding Author
of advice I received was to contact the PI in advance and invite *E-mail: ariane.nunes-alves@h-its.org.
her or him for a coffee or volunteer to give an informal talk to ORCID
her or his laboratory, in case the laboratory happened to be Ariane Nunes-Alves: 0000-0002-5488-4732
close to one of the conferences I was going to attend. I never
Notes
had the courage to do this because I thought of PIs as very
The author declares no competing financial interest.


busy people who would not have time to spend with Ph.D.
students. Now that I am more experienced, I know that most ACKNOWLEDGMENTS
PIs, despite being busy, would be happy to discuss their results ́ Dr. Neil Bruce, Dr. Kira
and hear about new ideas. I would like to thank Javier Diaz,
I started sending applications 10 months before my defense. Armacost, Dr. Bruno Chausse, and Dr. Csaba Daday for review
In most cases I sent unsolicited e-mails to PIs, and I also of this manuscript. I also thank the Coordenação de
́ Superior (Capes, process
Aperfeiçoamento de Pessoal de Nivel
applied to positions advertised on the Internet.13 I wrote
proposals to get independent funding for my postdoctoral number 88881.162167/2017-01) and the Alexander von
research too. I had some video conference interviews in the Humboldt Foundation, which support my work through a
United States and in Germany, and they usually went fine. Capes-Humboldt fellowship, and the Klaus Tschira Founda-
tion for financial support.


I got to the second round of selection of a postdoctoral
funding I applied to in Germany, and the interviews were
REFERENCES
conducted in person, with the travel expenses covered by the
research cluster offering the funding. I visited the laboratory of (1) Nunes-Alves, A.; Arantes, G. M. Ligand-receptor affinities
computed by an adapted linear interaction model for continuum
Prof. Dr. Rebecca Wade at the Heidelberg Institute for
electrostatics and by protein conformational averaging. J. Chem. Inf.
Theoretical Studies for a week, and I could see that her Model. 2014, 54, 2309−2319.
laboratory would be a very good match for me. Later, I was (2) Nunes-Alves, A.; Arantes, G. M. Mechanical unfolding of
awarded the postdoctoral funding, and I am currently working macromolecules coupled to bond dissociation. J. Chem. Theory
in her laboratory. Comput. 2018, 14, 282−290.
I started my postdoctoral position in January 2018, after (3) Nunes-Alves, A.; Zuckerman, D. M.; Arantes, G. M. Escape of a
which I faced new challenges. I am still not fully adjusted to the small molecule from inside T4 lysozyme by multiple pathways.
German winter, which usually gets much colder than winters in Biophys. J. 2018, 114, 1058−1066.
Brazil. I did not speak any German when I arrived, which is not (4) Soares, T. A.; Wahab, H. A. Molecular simulation in Latin
a problem in the laboratory, but basic tasks, like organizing an America: coming of age. J. Chem. Inf. Model. 2019, 59, 3601−3602.
(5) de Magalhães, C. S.; Almeida, D. M.; Barbosa, H. J. C.;
Internet connection, can be a hurdle. I counted on the help Dardenne, L. E. A dynamic niching genetic algorithm strategy for
and kindness of my German laboratory mates to work it out. docking highly flexible ligands. Inf. Sci. 2014, 289, 206−224.
Something that made my life easier was the company and (6) DockThor. https://www.dockthor.lncc.br/v2/ (accessed 2019-
support of my husband, who left his job in Brazil to come with 08-20).
me to Germany. (7) Maia, J. D.; Urquiza Carvalho, G. A.; Mangueira, C. P. J.;
My expectations have so far been fulfilled. I have been Santana, S. R.; Cabral, L. A.; Rocha, G. B. GPU linear algebra libraries
studying drug binding kinetics from a different perspective. I and GPGPU programming for accelerating MOPAC semiempirical
am currently using methods such as Brownian dynamics and quantum chemistry calculations. J. Chem. Theory Comput. 2012, 8,
molecular dynamics simulations to see how the motion of 3072−3081.
(8) Netz, P. A.; Potestio, R.; Kremer, K. Adaptive resolution
small drug-like molecules is affected by macromolecular
simulation of oligonucleotides. J. Chem. Phys. 2016, 145, 234101.
crowding, the usual condition inside cells,14 characterized by (9) Armacost, K. A. The transition from academia: overcoming the
a high concentration of macromolecules such as proteins and barrier to a career in the drug discovery industry. J. Chem. Inf. Model.
lipids. My professional network is growing. There were also 2018, 58, 1161−1163.
some personal benefits: I am more flexible, have learned the (10) Volkamer, A.; Riniker, S. Transition from academia to industry
basics of German, and have managed to travel to nearby places and back. J. Chem. Inf. Model. 2018, 58, 1469−1472.

B DOI: 10.1021/acs.jcim.9b00764
J. Chem. Inf. Model. XXXX, XXX, XXX−XXX
Journal of Chemical Information and Modeling Perspective

(11) Copeland, R. A. The drug-target residence time model: a 10-


year retrospective. Nat. Rev. Drug Discovery 2016, 15, 87−95.
(12) Schuetz, D. A.; et al. Kinetics for Drug Discovery: an industry-
driven effort to target drug residence time. Drug Discovery Today
2017, 22, 896−911.
(13) Computational Chemistry List. http://www.ccl.net/ (acessed
2019-09-20).
(14) Phillip, Y.; Schreiber, G. Formation of protein complexes in
crowded environments − From in vitro to in vivo. FEBS Lett. 2013,
587, 1046−1052.

C DOI: 10.1021/acs.jcim.9b00764
J. Chem. Inf. Model. XXXX, XXX, XXX−XXX

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