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  • Laboratory of Biomodelling Filipek Laboratory

Laboratory of Biomodelling Filipek Laboratory

 
1. Studies of activation mechanisms of G-proteincoupled receptors

Recent crystal structures of class A (rhodopsin-like) G-protein-coupled receptors (GPCRs), namely β1- and β2- adrenergic receptors and adenosine A2A receptors, showed nearly identical transmembrane domain structures but differences in the states of molecular switches compared with rhodopsin, which was the first GPCR crystallized. Based on experimental data, agonist binding and receptor activation were proposed to occur through a series of conformational intermediates. The transition between these intermediate states involves disruption, creation, or reorganization of intramolecular interactions that stabilize the basal state of a receptor. These changes are elicited by the action of molecular switches (also called microswitches).
The major switches proposed so far for different GPCRs, reflecting shared activation mechanisms, include the “rotamer toggle switch” that involves the CWxPx(F/H) sequence on transmembrane helix TM6, the switch based on the NPxxY(x)(5,6)F sequence that links helices TM7 and H8, and the “ionic lock” that links transmembrane helices TM3 and TM6 and employs the (E/D)RY motif on TM3. There are also switches not assigned to any particular sequence motifs, such as the 3-7 lock that involves the interaction between TM3 and TM7 and is present only in selected receptor types.
In our earlier papers, we investigated early activation steps that occur simultaneously to ligand binding in the MOR (mu), DOR (delta), and KOR (kappa) opioid receptors. The first switch that was broken by agonist binding was the “3-7 lock,” a hydrogen bond D3.32-Y7.43 that links transmembrane helices TM3 and TM7. It was the first activation event observed. We also detected the action of a second switch: a rotamer toggle switch that involves  a simultaneous change of side chain conformations of W6.48 and adjacent residues and was therefore called the extended toggle switch. In the case of opioid receptors, the other residue in this extended switch was H6.52. This residue also participated in the agonist-antagonist sensor, determined by the propensity for creating a hydrogen bond with Y3.33 for antagonists and H6.52 for agonists.
All studied ligands, analogs of morphine with a common tyramine structural scaffold, created a salt bridge with D3.32 with their protonated nitrogen atom of the tyramine group. This sensor was studied by us for MOR and later DOR and KOR. The proposed mechanism of its action was later confirmed by molecular dynamics simulations of a closely related agonist-antagonist pair of KOR ligands: 5’-GNTI and 6’-GNTI.
Cannabinoid receptors, similarly to opioid receptors, belong to class A (similar to rhodopsin) GPCRs. The docking of agonists and antagonists to cannabinoid CB1 and CB2 receptors revealed the importance of a centrally located rotamer toggle switch and its possible participation in the mechanism of agonist/antagonist recognition. The switch is composed of two residues, F3.36 and W6.48, located on opposite transmembrane helices TM3 and TM6 (which is dissimilar to other GPCRs) in the central part of the membranous domain of cannabinoid receptors. The CB1 and CB2 receptor models were constructed based on the adenosine A2A receptor template. The two best-scored conformations of each receptor were used for the docking procedure. In all poses (ligand-receptor conformations) characterized by the lowest ligand-receptor intermolecular energy and free energy of binding, the ligand type matched the state of the rotamer toggle switch; antagonists maintained an inactive state of the switch, whereas agonists changed it.

2. Structure of presenilin, a component of γ-secretase

The integral membrane protein ensemble γ-secretase is responsible for the proteolytic processing of various type I transmembrane domains, among them the amyloid precursor protein, whose final cleavage results in the release of the amyloid β peptide which is the major component of senile plaques found in Alzheimer’s disease. The catalytic activity of γ-secretase requires the endoproteolytic cleavage of its presenilin subunit during the maturation of the complex. The cleavage results in the generation of natural N- and C-terminal presenilin fragments, each of which harbors one of the two active-site aspartates that contribute to the formation of a hydrophilic cavity where catalysis is believed to occur. The N-terminal fragment of presenilin-1 is believed to have a classical transmembrane topology, consistent with all published models. Biochemical studies and topology predictions performed on the C-terminal fragment (CTF), however, have thus far yielded a plethora of ambiguous and contradictory results, which may be difficult to reconcile in the absence of structural information. By employing NMR measurements on cell-free expressed protein in SDS micelles, determining the first structural model of the C-terminal fragment of human presenilin-1 was possible. The structure revealed a topology by which the membrane would likely be traversed three times, consistent with the more generally accepted model, but contain unique structural features that may be adapted to accommodate the unusual intramembrane catalytic process and could account for the lack of consensus observed in most studies.
To further evaluate the structure of CTF, we performed molecular dynamics (MD) simulations both in micelles and in a lipid bilayer. To achieve the sufficient simulation time needed for micelle formation and extensive sampling of the conformational space, we chose a coarse-grain approach using the MARTINI method, which was primarily developed to study the behavior of large biological membrane systems. Simulations were performed with 200 coarse-grain dodecyl-phosphocholine (DPC) molecules, which formed a micelle consisting of approximately 80 molecules around CTF during the first 50 ns, during which time the structure of CTF was frozen. In the ensuing 3 γs simulation, the coarse-grain structure of CTF was allowed to change. The comparison with the initial NMR structure revealed that the interhelical angle between helices 7 and 8 remained relatively stable (140° in the NMR structure and 120° after the 3 γs simulation), and helices 9a and 9b became more antiparallel (105° in the NMR structure and 130° after the simulation).
We also performed coarse-grained simulations in DLPC (dilauroylphosphatidylcholine) and DPPC (dipalmitoylphosphatidyl-choline) bilayers using the MARTINI method and MD simulations of allatom representation of CTF by employing continuous environments with the Implicit Membrane Model (IMM1) method in the CHARMM program. As expected, the resulting structures showed larger differences both with respect to the NMR input structure and to each other.
Although the angle between helices 7 and 8 remained relatively stable, the angle between helices 9a and 9b changed depending on the thickness of the membrane.
Additionally, the position of the catalytic helix also shifted from the center of the membrane toward its border, again depending on the membrane width. Notably, however, in the present case, the bilayer is not necessarily a better suited environment than a micelle because several elements of CTF are believed to reside in close proximity or even contribute to the formation of the water-filled cavity that exists within the γ-secretase complex. In such a case, the more accommodating micelle may indeed provide a better hydrophobic environment for CTF in the absence of the other γ-secretase components.

(activity discontinued since July, 2010)

Lab Leader:
Sławomir Filipek, PhD, DSc Habil


Senior Researchers:
Michał Koliński, PhD
Dorota Latek, PhD
Szymon Niewieczerzał, PhD
Bartosz Trzaskowski, PhD


Junior Researchers:

Aleksander Dębiński, MSc
Umesh Ghoshdastider, MSc
Krzysztof Młynarczyk, MSc
Wojciech Puławski, MSc

2013

Latek D, Pasznik P, Carlomagno T, Filipek S

Towards Improved Quality of GPCR Models by Usage of Multiple Templates and Profile-Profile Comparison

Pulawski W, Filipek S, Zwolinska A, Debinski A, Krzysko K, Garduño-Juárez R, Viswanathan S, Renugopalakrishnan V

Low-temperature molecular dynamics simulations of horse heart cytochrome c and comparison with inelastic neutron scattering data

Wu Y, Yuan S, Chen S, Wu D, Chen J, Wu J

Enhancing the production of galacto-oligosaccharides by mutagenesis of Sulfolobus solfataricus β-galactosidase

Dudzik J, Chang WC, Kannan AM, Filipek S, Viswanathan S, Li P, Renugopalakrishnan V, Audette GF

Cross-linked glucose oxidase clusters for biofuel cell anode catalysts

2012

Trzaskowski B, Latek D, Yuan S, Ghoshdastider U, Debinski A, Filipek S

Action of Molecular Switches in GPCRs - Theoretical and Experimental Studies

Yuan S, Ghoshdastider U, Trzaskowski B, Latek D, Debinski A, Pulawski W, Wu R, Gerke V, Filipek S

The Role of Water in Activation Mechanism of Human N-Formyl Peptide Receptor 1 (FPR1) Based on Molecular Dynamics Simulations

Naldi M, Fiori J, Pistolozzi M, Drake AF, Bertucci C, Wu R, Mlynarczyk K, Filipek S, De Simone A, Andrisano V

Amyloid β-Peptide 25-35 Self-Assembly and Its Inhibition: A Model Undecapeptide System to Gain Atomistic and Secondary Structure Details of the Alzheimer's Disease Process and Treatment

Pulawski W, Ghoshdastider U, Andrisano V, Filipek S

Ubiquitous amyloids

2011

Audette GF, Lombardo S, Dudzik J, Arruda TM, Kolinski M, Filipek S, Mukerjee S, Kannan AM, Thavasi V, Ramakrishna S, Chin M, Somasundaran P, Viswanathan S, Keles RS, Renugopalakrishnan V

Modeling of ligand binding to G protein coupled receptors: cannabinoid CB(1), CB (2) and adrenergic β (2)AR.

Koch R, Lipton AS, Filipek S, Renugopalakrishnan V

Arginine interactions with anatase TiO(2) (100) surface and the perturbation of (49)Ti NMR chemical shifts - a DFT investigation: relevance to Renu-Seeram bio solar cell

Latek D, Kolinski M, Ghoshdastider U, Debinski A, Bombolewski R, Plazinska A, Jozwiak K, Filipek S

Modeling of ligand binding to G protein coupled receptors: cannabinoid CB(1), CB (2) and adrenergic β (2)AR

2010

Zurawska A, Urbanski J, Matuliene J, Baraniak J, Klejman MP, Filipek S, Matulis D, Bieganowski P

Mutations that increase both Hsp90 ATPase activity in vitro and Hsp90 drug resistance in vivo.

Kolinski M, Filipek S

Study of a structurally similar kappa opioid receptor agonist and antagonist pair by molecular dynamics simulations.

2009

J.S. Jaworski, A. Kosson, S. Filipek, M. Kolinski, D. Kuck

Properties of Radical Anions of Triptindanones and Indanones: Electronic Communication and Stability of Ion Pairs Containing Lithium Cations

Park PS, Sapra KT, Jastrzebska B, Maeda T, Maeda A, Pulawski W, Kono M, Lem J, Crouch RK, Filipek S, Müller DJ, Palczewski K

Modulation of molecular interactions and function by rhodopsin palmitylation

S. Filipek

“Bioinformatyka strukturalna białek transbłonowych”

V. Renugopalakrishnan, A. M. Kannan, S. Srinivasan, V. Thavasi, S. Ramakrishna, P. Li, A. Mershin, S. Filipek, A. Kumar, J. Dutta, A. Jaya, L. Munukutla, S. Velumani, G. F. Audette

“Nanomaterials for Energy Convertion Applications”

Kannan AM, Renugopalakrishnan V, Filipek S, Li P, Audette GF, Munukutla L

Bio-batteries and bio-fuel cells: leveraging on electronic charge transfer proteins.

Thavasi V, Lazarova T, Filipek S, Kolinski M, Querol E, Kumar A, Ramakrishna S, Padrós E, Renugopalakrishnan V

Study on the feasibility of bacteriorhodopsin as bio-photosensitizer in excitonic solar cell: a first report.

Austermann J, Nazmi AR, Heil A, Fritz G, Kolinski M, Filipek S, Gerke V

Generation and characterization of a novel, permanently active S100P mutant.

Kilanczyk E, Filipek S, Jastrzebska B, Filipek A

CacyBP/SIP binds ERK1/2 and affects transcriptional activity of Elk-1

M. Kolinfski, S. Filipek

Studies of the Activation Steps Concurrent to Ligand Binding in δOR and κOR Opioid Receptors Based on Molecular Dynamics Simulations

2008

Majewski T, Lee S, Jeong J, Yoon DS, Kram A, Kim MS, Tuziak T, Bondaruk J, Lee S, Park WS, Tang KS, Chung W, Shen L, Ahmed SS, Johnston DA, Grossman HB, Dinney CP, Zhou JH, Harris RA, Snyder C, Filipek S, Narod SA, Watson P, Lynch HT, Gazdar A, Bar-Eli M,

Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy.

Stephen R, Filipek S, Palczewski K, Sousa MC

Ca2+ -dependent regulation of phototransduction.

Bhatia P, Kolinski M, Moaddel R, Jozwiak K, Wainer IW

Determination and modelling of stereoselective interactions of ligands with drug transporters: a key dimension in the understanding of drug disposition

Jozwiak K, Krzysko KA, Bojarski L, Gacia M, Filipek S

Molecular models of the interface between anterior pharynx-defective protein 1 (APH-1) and presenilin involving GxxxG motifs

Kolinski M, Filipek S.

Molecular dynamics of mu opioid receptor complexes with agonists and antagonists

2007

Park PS, Sapra KT, Koliński M, Filipek S, Palczewski K, Muller DJ

Stabilizing effect of Zn2+ in native bovine rhodopsin

Lee S, Jeong J, Majewski T, Scherer SE, Kim MS, Tuziak T, Tang KS, Baggerly K, Grossman HB, Zhou JH, Shen L, Bondaruk J, Ahmed SS, Samanta S, Spiess P, Wu X, Filipek S, McConkey D, Bar-Eli M, Issa JP, Benedict WF, Czerniak B

Forerunner genes contiguous to RB1 contribute to the development of in situ neoplasia.

Krzysko KA, Kolinski M, Filipek S.

Molecular modelling of the complex of oligomeric rhodopsin and its G protein.

Golan MP, Styczyńska M, Jóźwiak K, Walecki J, Maruszak A, Pniewski J, Lugiewicz R, Filipek S, Zekanowski C, Barcikowska M

Early-onset Alzheimer's disease with a de novo mutation in the presenilin 1 gene

2006

Jaworski JS, Cembor M, Koliński M

Electrostatic model of bond dissociation energies in polyhalogen methanes

Zhu L, Imanishi Y, Filipek S, Alekseev A, Jastrzebska B, Sun W, Saperstein DA, Palczewski K

Autosomal recessive retinitis pigmentosa and E150K mutation in the opsin gene.

Zekanowski C, Golan MP, Krzyśko KA, Lipczyńska-Łojkowska W, Filipek S, Kowalska A, Rossa G, Pepłońska B, Styczyńska M, Maruszak A, Religa D, Wender M, Kulczycki J, Barcikowska M, Kuźnicki J.

Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment.

Tanuj Sapra K, Park PS, Filipek S, Engel A, Müller DJ, Palczewski K

Detecting molecular interactions that stabilize native bovine rhodopsin

Modzelewska A, Filipek S, Palczewski K, Park PS

Arrestin interaction with rhodopsin: conceptual models.

Jozwiak K, Zekanowski C, Filipek S

Linear patterns of Alzheimer's disease mutations along alpha-helices of presenilins as a tool for PS-1 model construction

Cieplak M, Filipek S, Janovjak H, Krzyśko KA

Pulling single bacteriorhodopsin out of a membrane: Comparison of simulation and experiment.

2005

Sokal I, Dupps WJ, Grassi MA, Brown J Jr, Affatigato LM, Roychowdhury N, Yang L, Filipek S, Palczewski K, Stone EM, Baehr W

A novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)

Filipek S, Modzelewska A, Krzysko KA

Functional oligomers of rhodopsin – a G protein-coupled receptor template

Filipek S

Organization of rhodopsin molecules in native membranes of rod cells--an old theoretical model compared to new experimental data.

2004

Zekanowski C, Religa D, Graff C, Filipek S, Kuźnicki J

Genetic aspects of Alzheimer's disease

Zhu L, Jang GF, Jastrzebska B, Filipek S, Pearce-Kelling SE, Aguirre GD, Stenkamp RE, Acland GM, Palczewski K

A naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor.

Suda K, Filipek S, Palczewski K, Engel A, Fotiadis D

The supramolecular structure of the GPCR rhodopsin in solution and native disc membranes.

Park PS, Filipek S, Wells JW, Palczewski K

Oligomerization of G protein-coupled receptors: past, present, and future.

Liang Y, Fotiadis D, Maeda T, Maeda A, Modzelewska A, Filipek S, Saperstein DA, Engel A, Palczewski K

Rhodopsin signaling and organization in heterozygote rhodopsin knockout mice

Jastrzebska B, Maeda T, Zhu L, Fotiadis D, Filipek S, Engel A, Stenkamp RE, Palczewski K

Functional characterization of rhodopsin monomers and dimers in detergents

Imanishi Y, Yang L, Sokal I, Filipek S, Palczewski K, Baehr W

Diversity of guanylate cyclase-activating proteins (GCAPs) in teleost fish: characterization of three novel GCAPs (GCAP4, GCAP5, GCAP7) from zebrafish (Danio rerio) and prediction of eight GCAPs (GCAP1-8) in pufferfish (

Fotiadis D, Liang Y, Filipek S, Saperstein DA, Engel A, Palczewski K

The G protein-coupled receptor rhodopsin in the native membrane

Filipek S, Krzysko KA , Fotiadis D, Liang Y, Saperstein DA, Engel A, Palczewski K

A concept for G protein activation by G protein-coupled receptor dimers: the transducin/rhodopsin interface

2003

Nowotny M, Spiechowicz M, Jastrzebska B, Filipek A, Kitagawa K, Kuznicki J

Calcium-regulated interaction of Sgt1 with S100A6 (calcyclin) and other S100 proteins

Schadel SA, Heck M, Maretzki D, Filipek S, Teller DC, Palczewski K, Hofmann KP

Ligand channeling within a G-protein-coupled receptor. The entry and exit of retinals in native opsin.

Noorwez SM, Kuksa V, Imanishi Y, Zhu L, Filipek S, Palczewski K, Kaushal S

Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa.

Mirzadegan T, Benkö G, Filipek S, Palczewski K

Sequence analyses of G-protein-coupled receptors: similarities to rhodopsin.

Maeda T, Van Hooser JP, Driessen CA, Filipek S, Janssen JJ, Palczewski K

Evaluation of the role of the retinal G protein-coupled receptor (RGR) in the vertebrate retina in vivo.

Liang Y, Fotiadis D, Filipek S, Saperstein DA, Palczewski K, Engel A

Organization of the G protein-coupled receptors rhodopsin and opsin in native membranes

Liang Y, Fotiadis D, Filipek S, Saperstein DA, Palczewski K, Engel A

Organization of the G protein-coupled receptors rhodopsin and opsin in native membranes.

Fritze O, Filipek S, Kuksa V, Palczewski K, Hofmann KP, Ernst OP

Role of the conserved NPxxY(x)5,6F motif in the rhodopsin ground state and during activation.

Fotiadis D, Liang Y, Filipek S, Saperstein DA, Engel A, Palczewski K

Atomic-force microscopy: Rhodopsin dimers in native disc membranes

Filipek S, Teller DC, Palczewski K, Stenkamp R

The crystallographic model of rhodopsin and its use in studies of other G protein-coupled receptors.

2002

Kuksa V, Bartl F, Maeda T, Jang GF, Ritter E, Heck M, Van Hooser JP, Liang Y, Filipek S, Gelb MH, Hofmann KP, Palczewski K

Biochemical and physiological properties of rhodopsin regenerated with 11-cis-6-ring- and 7-ring-retinals.