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Posts tagged ‘Skrynnikov’

Gordon Research Conference on Diffraction Methods

Posted: 17.07.2016

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Nikolai Skrynnikov presented talk “Motions of Protein Molecules Within the Crystalline Lattice” at the Gordon Research Conference on Diffraction Methods, Bates College, ME, USA, 17-22 Jul 2016.

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XXXVIII Finnish NMR Symposium

Posted: 13.06.2016

Finnish NMR symposium

Nikolai Skrynnikov, Ivan Podkorytov, Sergei Izmailov, Olga Rogacheva, Kerstin Kaempf and Sevastyan Rabdano attended XXXVIII Finnish NMR Symposium, Jyvaskyla, Finland.

Nikolai Skrynnikov presented lecture “Dynamics in Protein Crystals: Insights From MD Simulations Complement New Solid-State NMR And X-Ray Data”.

Kerstin Kaempf presented oral talk “Local and global dynamics of intrinsically disordered proteins: a case study of H4 histone tail“.

Ivan Podkorytov presented poster “Diffusion-filtered experiment to detect flexible portion of protein chain in amyloid fibrils: application to Sup35NM“.

Sergei Izmailov presented poster “Simple MD-based model for oxidative folding of peptides and proteins”.

Olga Rogacheva presented poster “Using molecular dynamics simulation and chemical shift prediction to unravel dynamics in different crystal forms of ubiquitin”.

Sevastyan Rabdano presented poster “Loss of protein stability due to formation of intermolecular disulfide bonds under the effect of oxidative stress: case study of the RRM2 domain from neuropathological protein TDP-43”.

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Dynamics in Protein Crystals

Posted: 01.06.2016

We have investigated dynamics in two crystal forms of ubiquitin (PDB entries 3ONS and 3N30) with particular emphasis on (i) conformational exchange between β turn type I and II in the region 51-54 and (ii) rocking dynamics where protein molecules as a whole undergo subtle reorientational motion within the confines of the crystal lattice. Experimentally, both motional processes have been probed using relaxation dispersion solid state NMR techniques and showed similar or identical characteristic times (tens of microseconds) in 3N30 crystals. This raise a question: is this merely a coincidence or, otherwise, are these two motional modes coupled? To answer this question we performed MD simulations of 3ONS and 3N30 crystals. To quantify the effect of rocking motion we have used temporal correlation functions.

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Crystal MD simulations provide useful insight into rocking motion. We demonstrated that 3N30 crystal is prone to rocking and observed a weak coupling between rocking motion and βI↔βII exchange. Our data are also supported by X-Ray and ssNMR evidence and appear to be quite accurate in explaining the population balance between different conformations.

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International Symposium “Magnetic resonance: from fundamental research to practical applications” Kazan

Posted: 23.04.2016

Kazan conference

http://kpfu.ru/science/konferencii/magnitnyj-rezonans-ot-fundamentalnyh-issledovanij/fotogalereya

Nikolai and Kerstin took part in the international symposium “Magnetic Resonance: from fundamental research to practical applications” in Kazan, 21-23 Apr 2016.

Kerstin presented a poster entitled “Local and global dynamics of disordered proteins via the combination of temperature-dependent NMR spin relaxation measurements and MD simulations: a case study of H4 histone tail”. For the poster presentation she was awarded with one of the poster prizes.

Nikolai presented talk “Dynamics in protein crystals: insights from MD simulations complement new ssNMR and x-ray data”.

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Dynamics in protein crystals: insights from MD simulations complement new ssNMR and x-ray data

Posted: 10.04.2016

57th Experimental Nuclear Magnetic Resonance Conference (ENC), Pittsburgh PA, 10-15 Apr 2016

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Nikolai Skrynnikov presented talk “Dynamics in protein crystals: insights from MD simulations complement new ssNMR and X-ray data” at the 57th Experimental Nuclear Magnetic Resonance Conference (ENC), Pittsburgh PA, 10-15 Apr 2016.

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XII International Workshop On Magnetic Resonance, Rostov-on-Don

Posted: 02.03.2015

Sergei Izmailov, Sevastyan Rabdano, Ivan Podkorytov and Nikolai Skrynnikov attended conference “XII International Symposium on Magnetic Resonance (Spectroscopy, Imaging & Ecology)”, Rostov-on-Don, Russia, 2-6 March 2015.

Nikolai Skrynnikov presented lecture “Probing protein dynamics by NMR experiments and MD simulations”.

Sevastyan presented an oral talk “Destabilization of RNA-Recognition Motif RRM2 In Proteinopathic Protein TDP-43 Under the Effect of Oxidative Stress”.

Sergei Izmailov presented a poster entitled “Molecular dynamics simulation of folding of cysteine-containing peptide guanylin with formation of disulfide bonds”

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Modeling a system with intrinsic disorder: an NMR/MD study of peptide-protein encounter complex

Posted: 24.08.2014

International Conference on Magnetic Resonance in Biological Systems (ICMRBS)

Nikolai Skrynnikov has attended the International Conference on Magnetic Resonance in Biological Systems (ICMRBS), Dallas, TX, 24-29 Aug 2014. He presented the lecture “Modeling a system with intrinsic disorder: an NMR/MD study of peptide-protein encounter complex”.

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RRM2 1H, 13C, 15N chemical shifts

Posted: 11.06.2014

On May 2, 2014 in repository Biological Magnetic Resonance Data Bank the assignments of 1H, 13C and 15N chemical shifts for RRM2 domain of TDP-43 protein was published.

Authors: Rabdano, Sevastyan; Podkorytov, Ivan; Yuwen, Tairan; Groves, Adam; Chamberlain, Kyle; Yakimov, Alexander; Skrynnikov, Nikolai.

BMRB 19922

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NMRCM 2014

Posted: 07.06.2014

Members of the laboratory took active part in conference Nuclear Magnetic Resonance in Condenced Matter “Biomolecular NMR and related phenomena”, Saint Petersburg, July 7-11, 2014.

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Nikolai Skrynnikov presented the lecture

  • T. Yuwen, Yi Xue, F. Zhu and N.R. Skrynnikov Modeling a system with intrinsic disorder: an NMR/MD study of peptide-protein encounter complex.

Sevastyan Rabdano presented oral talk

  • The study of hydration properties of functional groups of glycine and beta- alanine amino acids by nuclear magnetic resonance and quantum chemical calculations.

All member of laboratory participated in discussion of lectures, oral and poster presentations at the NMRCM 2014.

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CP-HISQC: a better version of HSQC experiment for intrinsically disordered proteins under physiological conditions

Posted: 04.05.2014

Yuwen, T. & Skrynnikov, N. R. CP-HISQC: a better version of HSQC experiment for intrinsically disordered proteins under physiological conditions. Journal of Biomolecular NMR 58, 175–192 (2014).

DOI: 10.1007/s10858-014-9815-5

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