Wojciech Paslawski
Research Specialist
E-mail: wojciech.paslawski@ki.se
Visiting address: BioClinicum J5:20, Akademiska stråket 1, Karolinska universitetssjukhu, 17164 Solna
Postal address: K8 Klinisk neurovetenskap, K8 Neuro Svenningsson, 171 77 Stockholm
About me
- I am currently working as Assistant Professor in Per Svennigsson group. My
position is currently purely research based.
I am working in a Parkinson’s
disease (PD) field for 11 years. My scientific carrier started with
biophysical examination of alpha-synuclein (aSN) oligomeric species, which
are believed to be the most toxic species in PD, and resulted with
gathering methodological expertise in many scientific techniques. During
post-doctoral training I extrapolated the pure biophysical protein-protein
interaction process towards neurotoxicity culprits of aSN. From that point
my interest were pointed to the basic research
dedicated to aSN neurotoxicity in cellular models, its interactions with
other protein and molecules. The post-doctoral training in the
multidisciplinary team, with ongoing academic and clinical research related
to PD and other parkinsonian syndromes, extended my research focus and let
me be involved in projects involving among other the depression
mechanism and immunological studies. Consequently, during my current work
as a assistant professor, I am also put part of my research focus into other
parkinsonian syndromes and the selective vulnerability of neurons
in PD pathology.
*Research Support*
*Source:* Åke Wibergs foundation Research Grant
*Role:* PI
*Title:* The role of brain cholesterol and steroids in Parkinson’s disease
pathology
*Source:* The Michael J. Fox Foundation for Parkinson's Research
*Role:* co-PI
*Title:* Assessment of apolipoproteins and alpha-synuclein in lipoprotein
vesicles in cerebrospinal fluid
*Source:* Karolinska Institute Research Grant
*Role:* PI
*Title:* Steroids in neurodegeneration
*2010-2014 Aarhus University, Department of Molecular Biology and
Genetics, PhD in Nanoscience*
*Supervisor: *Daniel Otzen, Professor, Ph.D.
My PhD project was focused on studying a protein folding and its malfunction
in amyloid diseases. It engaged the biophysical characterization of protein
aggregates involved in aforementioned disorders and large screening for
potential compounds that can inhibit amyloid formation. The second part of
the project was dedicated to characterization of GlpG membrane protein
folding and how mutations in protein sequence disturb this process.
*2005-2010 **Wroclaw University of Technology, Department of
Chemistry, MSc Eng. in Molecular Biotechnology and Biocatalysis*
*Supervisor: *Krzysztof Pawlik, Ph.D.
My early research and Master thesis work was performed in microbiology filed
and included working with /Streptomyces/ bacteria, the largest
antibiotic-producing genus, generating antibacterial, antifungal, and
antiparasitic drugs, and also a wide range of other bioactive compounds. The
main aim of assignment was characterization of CpkF protein and its role in
secretion of one of the bioactive compounds by/ S. coelicolor/.
Research
- Currently I am focused on finding new potential biomarkers (proteins and
small compounds) for detection early onset of Parkinson’s disease (PD), as
well as related disorders, and solving mystery of selective vulnerability of
dopaminergic neurons in PD pathology. For the analysis I am mostly using
cerebrospinal fluid, but also plasma and other tissues, as it is the
preferred biosample to address diagnostic and prognostic information related
to neurodegenerative disorders. This research is important, since PD shares
symptomatology with several other rare neurodegenerative disorders
collectively named atypical parkinsonism syndromes (APS). APS include
corticobasal syndrome (CBS), progressive supranuclear palsy (PSP), multiple
system atrophy (MSA), vascular parkinsonism and dementia with Lewy bodies
(DLB). Therefore, in my research I am trying to target challenges caused by
the overlapping clinical features of PD and APS and find the targets able to
accurately discriminate between ATP and PD what will be critical for patients
as the disease progression, and subsequent functional decline, is often more
rapid in atypical parkinsonism syndromes.
I am also working with a protein purification and biophysics since beginning
of my PhD, mainly focusing on α-synuclein protein. I was working on
characterization of the oligomeric species of α-synuclein, which are
believed to be the most toxic species in PD. Currently, this part of my work
is targeted toward identifying new proteins interacting with fibrillar and
oligomeric α-synuclein.
*Publications*
Sousa VC, Mantas I, Stroth N, Hager T, Pereira M, Jiang H, Jabre S,
*Paslawski W*, Stiedl O, Svenningsson P. “*/P11 deficiency increases stress
reactivity along with HPA axis and autonomic hyperresponsiveness”, /*Mol
Psychiatry. 2021, Jul - 26(7):3253-3265. doi: 10.1038/s41380-020-00887-0. Epub
2020 Oct 1. PubMed PMID: 33005029.
*Paslawski W, * Bergström S, Zhang X, Remnestål J, He Y, Boxer A, Månberg
A, Nilsson P, Svenningsson P. “*/Cerebrospinal Fluid Proteins Altered in
Corticobasal Degeneration”, /* Mov Disord. 2021, Mar 4. doi:
10.1002/mds.28543. Epub ahead of print. PMID: 33660876.
Morató X, Garcia-Esparcia P, Argerich J, Llorens F, Zerr I, *Paslawski W*,
Borràs E, Sabidó E, Petäjä-Repo UE, Fernández-Dueñas V, Ferrer I,
Svenningsson P, Ciruela F. “*/Ecto-GPR37: a potential biomarker for
Parkinson's disease.”, /* Transl Neurodegener. 2021 Feb 26 - 10(1):8. doi:
10.1186/s40035-021-00232-7. PMID: 33637132 - PMCID: PMC7908677.
Markaki I, Bergström S, Tsitsi P, Remnestål J, Månberg A, Hertz E,
*Paslawski W*, Sorjonen K, Uhlén M, Mangone G, Carvalho S, Rascol O,
Meissner WG, Magnin E, Wüllner U, Corvol JC, Nilsson P, Svenningsson P.
“*/Cerebrospinal Fluid Levels of Kininogen-1 Indicate Early Cognitive
Impairment in Parkinson's Disease”, /* Mov Disord. 2020
Nov - 35(11):2101-2106. doi: 10.1002/mds.28192. Epub 2020 Aug 15. PMID:
33179332.
*Paslawski W*., Zareba-Paslawska J., Zhang X., Hölzl K., Wadensten H.,
Shariatgorji M., Janelidze S., Hansson O., Forsgren L., Andrén P.E.,
Svenningsson P., */“α-synuclein-lipoprotein interactions and elevated ApoE
level in cerebrospinal fluid from Parkinson's disease patients“, /* 2019,
PNAS, 116(30):15226-15235. doi: 10.1073/pnas.1821409116.
Olesen M.N., Christiansen J.R., Petersen S.V., Jensen P.H., *Paslawski W.*,
Romero-Ramos M., Sanchez-Guajardo V., */”/**/CD4 T cells react to local
increase of α-synuclein in a pathology-associated variant-dependent manner
and modify brain microglia in absence of brain pathology”, /*2018, Heliyon,
4(1), doi: 10.1016/j.heliyon.2018.e00513.
Paucar M., * *Beniaminov S., *Paslawski W.*, Svenningsson P., */“PSP-CBS
with Dopamine Deficiency in a Female with a FMR1 Premutation”/*, 2016,
Cerebellum, 15 (5), 636 -640, DOI: 10.1007/s12311-016-0793-x
*Paslawski W*, Mysling S, Thomsen K, Jørgensen T J D and Otzen DE,
*/“Co-existence of two different α-synuclein oligomers with different core
structures determined by Hydrogen/Deuterium Exchange Mass Spectrometry”,
/*Angew Chem Int Ed Engl 2014, 53 (29), p: 7560–63, doi:
101002/anie201400491
*Paslawski W*, Andreasen M, Nielsen S B, Lorenzen N, Thomsen K, Kaspersen J
D, Pedersen J S and Otzen D E, */“High stability and cooperative unfolding
of cytotoxic α-synuclein oligomers”, /*Biochemistry 2014, 53(39), p:
6252-63 doi: 101021/bi5007833
*Paslawski W*, Lillelund O, Kristensen J V, Schafer NP, Baker R P, Urban S
and Otzen D E, */ “Cooperative folding of a polytopic α-helical membrane
protein involves a compact N-terminal nucleus and nonnative loops”, /*PNAS
2015 Jun 30 - 112(26):7978-83 doi: 101073/pnas1424751112
*Paslawski W*, Lorenzen N, and Otzen D E, */“Formation and characterization
of α-synuclein oligomers”, /*Methods in Molecular Biology 2016
1345:133-50 doi: 101007/978-1-4939-2978-8_9
Lorenzen N, Nielsen S B, Kaspersen J D, Vad B S, Buell A K, Arosio P,
*Paslawski W*, Christiansen G, Valnickova Z, Andreasen M, Dobson C M, Enghild
J J, Knowles T P J, Pedersen J S and Otzen D E, */“The role of stable
α-synuclein oligomers in the molecular events underlying amyloid
formation”/*, J Am Chem Soc, 2014, 136 (10), p: 3859–68, doi:
101021/ja411577t
Pawlik K, *Paslawski W*, Buhl T, Kotowska M, */“Is protein CpkF from
Streptomyces coelicolor A3(2) associated with efflux of CPK polyketide? In
silico analysis”/*, SEPSIS, 2012, 2(4), p: 247—251, doi:
101066/S10025120007
*Paslawski W*, Pawlik K, */“Expression and study of CpkF transmembrane
protein from Streptomyces coelicolor A3(2)”/*, Prace Naukowe Wydziału
Chemicznego Politechniki Wrocławskiej nr 8, 2010, p:147-151
Articles
- Article: JOURNAL OF AFFECTIVE DISORDERS. 2024;349:286-296
- Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2024;25(1):683
- Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2023;24(22):16445
- Article: PARKINSONISM AND RELATED DISORDERS. 2023;116:105765
- Article: TRANSLATIONAL NEURODEGENERATION. 2023;12(1):42
- Article: STEM CELL REPORTS. 2023;18(1):337-353
- Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2022;23(22):14290
- Article: JOURNAL OF MOLECULAR NEUROSCIENCE. 2022;72(11):2313-2325
- Article: SCIENCE ADVANCES. 2022;8(34):eabo1543
- Article: NPJ PARKINSON'S DISEASE. 2022;8(1):71
- Article: FRONTIERS IN AGING NEUROSCIENCE. 2022;14:830704
- Article: MOLECULAR PSYCHIATRY. 2021;26(7):3253-3265
- Article: TRANSLATIONAL NEURODEGENERATION. 2021;10(1):8
- Article: MOVEMENT DISORDERS. 2020;35(11):2101-2106
- Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2019;116(30):15226-15235
- Article: CEREBELLUM. 2016;15(5):636-640
- Article: METHODS IN MOLECULAR BIOLOGY. 2016;1345:133-150
- Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2015;112(26):7978-7983
- Article: BIOCHEMISTRY. 2014;53(39):6252-6263
- Article: ANGEWANDTE CHEMIE INTERNATIONAL EDITION. 2014;53(29):7560-7563
- Article: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. 2014;136(10):3859-3868
- Show more
All other publications
- Letter: MOVEMENT DISORDERS. 2023;38(11):2136-2137
- Letter: MOVEMENT DISORDERS. 2021;36(5):1278-1280