TY - JOUR A1 - Knox-Brown, Patrick A1 - Rindfleisch, Tobias A1 - Günther, Anne A1 - Balow, Kim A1 - Bremer, Anne A1 - Walther, Dirk A1 - Miettinen, Markus S. A1 - Hincha, Dirk K. A1 - Thalhammer, Anja T1 - Similar Yet Different BT - Structural and Functional Diversity among Arabidopsis thaliana LEA_4 Proteins JF - International Journal of Molecular Sciences N2 - The importance of intrinsically disordered late embryogenesis abundant (LEA) proteins in the tolerance to abiotic stresses involving cellular dehydration is undisputed. While structural transitions of LEA proteins in response to changes in water availability are commonly observed and several molecular functions have been suggested, a systematic, comprehensive and comparative study of possible underlying sequence-structure-function relationships is still lacking. We performed molecular dynamics (MD) simulations as well as spectroscopic and light scattering experiments to characterize six members of two distinct, lowly homologous clades of LEA_4 family proteins from Arabidopsis thaliana. We compared structural and functional characteristics to elucidate to what degree structure and function are encoded in LEA protein sequences and complemented these findings with physicochemical properties identified in a systematic bioinformatics study of the entire Arabidopsis thaliana LEA_4 family. Our results demonstrate that although the six experimentally characterized LEA_4 proteins have similar structural and functional characteristics, differences concerning their folding propensity and membrane stabilization capacity during a freeze/thaw cycle are obvious. These differences cannot be easily attributed to sequence conservation, simple physicochemical characteristics or the abundance of sequence motifs. Moreover, the folding propensity does not appear to be correlated with membrane stabilization capacity. Therefore, the refinement of LEA_4 structural and functional properties is likely encoded in specific patterns of their physicochemical characteristics. KW - IDP KW - LEA protein KW - abiotic stress KW - dehydration KW - conformational rearrangement KW - membrane stabilization KW - sequence-structure-function relationship Y1 - 2020 U6 - https://doi.org/10.3390/ijms21082794 SN - 1422-0067 VL - 21 IS - 8 PB - Molecular Diversity Preservation International CY - Basel ER - TY - THES A1 - Knox-Brown, Patrick Frank T1 - Towards understanding the sequence-structure-function relationship of intrinsically disordered LEA_4 proteins from Arabidopsis thaliana N2 - Water-deficits can cause lethal damage to organisms, which is rooted in cellular dehydration. Many plant species, but also other organisms have developed mechanisms to tolerate such stresses, such as the expression of LEA proteins. Many studies report on physiological protective functions of LEA proteins but lack information about their precise mechanisms on a molecular level. Most LEA proteins are intrinsically disordered in dilute solution but may adopt a distinct secondary structure upon changes in solvent conditions. Understanding the molecular mechanism of how LEA proteins contribute to the counteraction of cellular damage during water-deficits may in the long-term pave the way for breeding crops that are resistant to the effects of global warming. The objective of the work at hand is to improve the biophysical understanding of the sequencestructure-function relationship of LEA proteins as membrane stabilizers, based on the LEA_4 family of the model plant A. thaliana. This is pursued by using a combination of spectroscopic and scattering techniques, supported by bioinformatics and computational analyses. Eight out of the 18 LEA_4 proteins are experimentally assessed revealing that a coil-helix transition in response to water-deficit is a common feature, as predicted for the entire family. In addition, they all stabilize simple membrane models during a freeze/ thaw cycle. Three-dimensional structure prediction of representative members suggests that their completely folded states are represented by a sequential arrangement of alpha-helical segments connected by unstructured linkers, which is experimentally verified for the LEA_4 protein COR15A. The unstructured linker region of COR15A represents a conserved motif among its closest homologs and is, therefore, of particular interest. Facilitating a set of seven designed and investigated COR15A mutants uncovers a complex interplay of transient interactions between the amphipathic alpha-helical segments, mediated by the linker, which fine-tunes folding transitions and structural ensembles upon reduced water-availability. Finally, alpha-helicity is also induced in COR15A upon temperature decrease, which is enhanced in the presence of osmolytes. In addition, high solution osmolarity induced secondary structure is followed by oligomerization of COR15A. Interestingly, the functionality of COR15A, in terms of liposome stabilization, strongly correlates with its alpha-helix ratio in the folded state. The present work significantly improves the understanding of the sequence-structure-function relationship for LEA_4 proteins and offers novel findings on folding mechanisms and oligomerization of COR15A. N2 - Wasserdefizite können zu letalem Schaden von Organismen führen, der letztendlich aus zellulärer Dehydrierung resultiert. Viele Pflanzen, aber auch andere Organismen haben Mechanismen entwickelt, um solche Stressfaktoren zu tolerieren, z.B. die Expression von LEAProteinen. Diverse Studien beschreiben deren physiologische Schutzfunktionen, es fehlen jedoch Informationen ihrer präzisen Mechanismen auf molekularer Ebene. Die meisten LEA-Proteine sind in wässriger Lösung intrinsisch unstrukturiert, können jedoch in Reaktion auf veränderte Lösungsmittelbedingungen geordnete Strukturen ausbilden. Ein solides Verständnis ihrer molekularen Mechanismen führt daher über die Entschlüsselung ihrer Sequenz-StrukturFunktions-Beziehungen, welche langfristig den Weg zur Entwicklung von Pflanzen ebnen, die Resistenzen gegen die Auswirkungen der globalen Erwärmung aufweisen.. Ziel der vorliegenden Arbeit ist, das Verständnis der Sequenz-Struktur-Funktions-Beziehung der LEA_4-Familie aus der Modellpflanze A. thaliana zu verbessern. Dazu wird eine Kombination von Spektroskopie- und Streutechniken (unterstützt durch prädiktive Computeranalysen) verwendet. Alle acht experimentell untersuchten der insgesamt 18 LEA_4-Proteine zeigen einen Coil-Helix-Übergang in Reaktion auf Wasserdefizit als gemeinsames Merkmal und stabilisieren einfache Membranmodelle während eines Gefrier-/ Tau-Vorgang. Die dreidimensionale Strukturvorhersage repräsentativer LEA_4-Proteine deutet an, dass der gefaltete Zustand einer Abfolge alpha-helikaler Segmente unterbrochen durch unstrukturierte Domänen entspricht, was für das LEA_4-Protein COR15A experimentell belegt wird. Der unstrukturierte Linker, der die beiden alpha-helikalen Segmente von COR15A verbindet, stellt ein Motiv dar, das innerhalb der nächsten Homologen konserviert ist und ist daher von besonderem Interesse. Mithilfe von sieben entworfenen und untersuchten COR15A-Mutanten kann der komplexe Zusammenhang transienter Wechselwirkungen zwischen den amphipathischen, alpha-helikalen Segmenten, vermittelt durch den Linker, gezeigt werden. Dieser spielt eine zentrale Rolle in der Feinabstimmung von Faltungsübergängen und strukturellen Ensembles bei verringerter Wasserverfügbarkeit. Ferner wird gezeigt, dass alpha-helikale Struktur auch durch Temperaturerniedrigung induziert werden kann, was in Gegenwart von Osmolyten stärker ausgeprägt ist. Hohe Osmolaritäten induzieren außerdem eine Oligomerisierung von COR15A. Interessanterweise korreliert die Funktionalität von COR15A (die Stabilisierung von Liposomen) stark mit dem relativen alpha-Helix-Anteil im gefalteten Zustand. Die vorliegende Arbeit verbessert erheblich das Verständnis für eine Sequenz-StrukturFunktions-Beziehung für LEA_4-Proteine und bietet neue Erkenntnisse zu Faltungsmechanismen und Oligomerisierung von COR15A. KW - IDPs KW - alpha-helix KW - coil-helix KW - linker KW - structure-function KW - protein-folding KW - LEA Y1 - 2021 ER - TY - JOUR A1 - Shou, Keyun A1 - Bremer, Anne A1 - Rindfleisch, Tobias A1 - Knox-Brown, Patrick A1 - Hirai, Mitsuhiro A1 - Rekas, Agata A1 - Garvey, Christopher J. A1 - Hincha, Dirk K. A1 - Stadler, Andreas M. A1 - Thalhammer, Anja T1 - Conformational selection of the intrinsically disordered plant stress protein COR15A in response to solution osmolarity - an X-ray and light scattering study JF - Physical chemistry, chemical physics : a journal of European Chemical Societies N2 - The plant stress protein COR15A stabilizes chloroplast membranes during freezing. COR15A is an intrinsically disordered protein (IDP) in aqueous solution, but acquires an alpha-helical structure during dehydration or the increase of solution osmolarity. We have used small- and wide-angle X-ray scattering (SAXS/WAXS) combined with static and dynamic light scattering (SLS/DLS) to investigate the structural and hydrodynamic properties of COR15A in response to increasing solution osmolarity. Coarse-grained ensemble modelling allowed a structure-based interpretation of the SAXS data. Our results demonstrate that COR15A behaves as a biomacromolecule with polymer-like properties which strongly depend on solution osmolarity. Biomacromolecular self-assembly occurring at high solvent osmolarity is initiated by the occurrence of two specific structural subpopulations of the COR15A monomer. The osmolarity dependent structural selection mechanism is an elegant way for conformational regulation and assembly of COR15A. It highlights the importance of the polymer-like properties of IDPs for their associated biological function. Y1 - 2019 U6 - https://doi.org/10.1039/c9cp01768b SN - 1463-9076 SN - 1463-9084 VL - 21 IS - 34 SP - 18727 EP - 18740 PB - Royal Society of Chemistry CY - Cambridge ER - TY - GEN A1 - Knox-Brown, Patrick A1 - Rindfleisch, Tobias A1 - Günther, Anne A1 - Balow, Kim A1 - Bremer, Anne A1 - Walther, Dirk A1 - Miettinen, Markus S. A1 - Hincha, Dirk K. A1 - Thalhammer, Anja T1 - Similar Yet Different BT - Structural and Functional Diversity among Arabidopsis thaliana LEA_4 Proteins T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - The importance of intrinsically disordered late embryogenesis abundant (LEA) proteins in the tolerance to abiotic stresses involving cellular dehydration is undisputed. While structural transitions of LEA proteins in response to changes in water availability are commonly observed and several molecular functions have been suggested, a systematic, comprehensive and comparative study of possible underlying sequence-structure-function relationships is still lacking. We performed molecular dynamics (MD) simulations as well as spectroscopic and light scattering experiments to characterize six members of two distinct, lowly homologous clades of LEA_4 family proteins from Arabidopsis thaliana. We compared structural and functional characteristics to elucidate to what degree structure and function are encoded in LEA protein sequences and complemented these findings with physicochemical properties identified in a systematic bioinformatics study of the entire Arabidopsis thaliana LEA_4 family. Our results demonstrate that although the six experimentally characterized LEA_4 proteins have similar structural and functional characteristics, differences concerning their folding propensity and membrane stabilization capacity during a freeze/thaw cycle are obvious. These differences cannot be easily attributed to sequence conservation, simple physicochemical characteristics or the abundance of sequence motifs. Moreover, the folding propensity does not appear to be correlated with membrane stabilization capacity. Therefore, the refinement of LEA_4 structural and functional properties is likely encoded in specific patterns of their physicochemical characteristics. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 901 KW - IDP KW - LEA protein KW - abiotic stress KW - dehydration KW - conformational rearrangement KW - membrane stabilization KW - sequence-structure-function relationship Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-469419 SN - 1866-8372 IS - 901 ER - TY - GEN A1 - Sowemimo, Oluwakemi T. A1 - Knox-Brown, Patrick A1 - Borcherds, Wade A1 - Rindfleisch, Tobias A1 - Thalhammer, Anja A1 - Daughdrill, Gary W. T1 - Conserved glycines control disorder and function in the cold-regulated protein, COR15A T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Cold-regulated (COR) 15A is an intrinsically disordered protein (IDP) from Arabidopsis thaliana important for freezing tolerance. During freezing-induced cellular dehydration, COR15A transitions from a disordered to mostly alpha-helical structure. We tested whether mutations that increase the helicity of COR15A also increase its protective function. Conserved glycine residues were identified and mutated to alanine. Nuclear magnetic resonance (NMR) spectroscopy was used to identify residue-specific changes in helicity for wildtype (WT) COR15A and the mutants. Circular dichroism (CD) spectroscopy was used to monitor the coil-helix transition in response to increasing concentrations of trifluoroethanol (TFE) and ethylene glycol. The impact of the COR15A mutants on the stability of model membranes during a freeze-thaw cycle was investigated by fluorescence spectroscopy. The results of these experiments showed the mutants had a higher content of alpha-helical structure and the increased alpha-helicity improved membrane stabilization during freezing. Comparison of the TFE- and ethylene glycol-induced coil-helix transitions support our conclusion that increasing the transient helicity of COR15A in aqueous solution increases its ability to stabilize membranes during freezing. Altogether, our results suggest the conserved glycine residues are important for maintaining the disordered structure of COR15A but are also compatible with the formation of alpha-helical structure during freezing induced dehydration. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1089 KW - COR15A KW - late embryogenesis abundant KW - intrinsically disordered proteins KW - trifluoroethanol KW - nuclear magnetic resonance Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-472217 SN - 1866-8372 IS - 1089 ER - TY - GEN A1 - Sowemimo, Oluwakemi A1 - Borcherds, Wade A1 - Knox-Brown, Patrick A1 - Rindfleisch, Tobias A1 - Thalhammer, Anja A1 - Daughdrill, Gary T1 - Evolution of Transient Helicity and Disorder in Late Embryogenesis Abundant Protein COR15A T2 - Biophysical journal N2 - Cold regulated protein 15A (COR15A) is a nuclear encoded, intrinsically disordered protein that is found in Arabidopsis thaliana. It belongs to the Late Embryogenesis Abundant (LEA) family of proteins and is responsible for increased freezing tolerance in plants. COR15A is intrinsically disordered in dilute solutions and adopts a helical structure upon dehydration or in the presence of co-solutes such as TFE and ethylene glycol. This helical structure is thought to be important for protecting plants from dehydration induced by freezing. Multiple protein sequence alignments revealed the presence of several conserved glycine residues that we hypothesize keeps COR15A from becoming helical in dilute solutions. Using AGADIR, the change in helical content of COR15A when these conserved glycine residues were mutated to alanine residues was predicted. Based on the predictions, glycine to alanine mutants were made at position 68, and 54,68,81, and 84. Labeled samples of wildtype COR15A and mutant proteins were purified and NMR experiments were performed to examine any structural changes induced by the mutations. To test the effects of dehydration on the structure of COR15A, trifluoroethanol, an alcohol based co solvent that is proposed to induce/stabilize helical structure in peptides was added to the NMR samples, and the results of the experiment showed an increase in helical content, compared to the samples without TFE. To test the functional differences between wild type and the mutants, liposome leakage assays were performed. The results from these assays suggest the more helical mutants may augment membrane stability. Y1 - 2019 U6 - https://doi.org/10.1016/j.bpj.2018.11.2553 SN - 0006-3495 SN - 1542-0086 VL - 116 IS - 3 SP - 473A EP - 473A PB - Cell Press CY - Cambridge ER - TY - JOUR A1 - Sowemimo, Oluwakemi T. A1 - Knox-Brown, Patrick A1 - Borcherds, Wade A1 - Rindfleisch, Tobias A1 - Thalhammer, Anja A1 - Daughdrill, Gary W. T1 - Conserved Glycines Control Disorder and Function in the Cold-Regulated Protein, COR15A JF - Biomolecules N2 - Cold-regulated (COR) 15A is an intrinsically disordered protein (IDP) from Arabidopsis thaliana important for freezing tolerance. During freezing-induced cellular dehydration, COR15A transitions from a disordered to mostly alpha-helical structure. We tested whether mutations that increase the helicity of COR15A also increase its protective function. Conserved glycine residues were identified and mutated to alanine. Nuclear magnetic resonance (NMR) spectroscopy was used to identify residue-specific changes in helicity for wildtype (WT) COR15A and the mutants. Circular dichroism (CD) spectroscopy was used to monitor the coil-helix transition in response to increasing concentrations of trifluoroethanol (TFE) and ethylene glycol. The impact of the COR15A mutants on the stability of model membranes during a freeze-thaw cycle was investigated by fluorescence spectroscopy. The results of these experiments showed the mutants had a higher content of alpha-helical structure and the increased alpha-helicity improved membrane stabilization during freezing. Comparison of the TFE- and ethylene glycol-induced coil-helix transitions support our conclusion that increasing the transient helicity of COR15A in aqueous solution increases its ability to stabilize membranes during freezing. Altogether, our results suggest the conserved glycine residues are important for maintaining the disordered structure of COR15A but are also compatible with the formation of alpha-helical structure during freezing induced dehydration. KW - COR15A KW - Late embryogenesis abundant KW - intrinsically disordered proteins KW - Trifluoroethanol KW - Nuclear magnetic resonance Y1 - 2019 U6 - https://doi.org/10.3390/biom9030084 SN - 2218-273X VL - 9 IS - 3 PB - MDPI CY - Basel ER -