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Biology subjects

Adams, P. G.

Publications and source records attributed to Adams, P. G..

7 recordsLinked to original sources

afMLevel: Deep learning U-Net Models for Levelling Atomic Force Microscopy Images and Movies

AFM experiments can now produce hundreds of frames per session and this rises to thousands in the case of video-rate high-speed AFM, but every image must still be levelled to remove tilt, bowing and line noise before it can be measured. Current automatic routines rely on user-chosen masks and parameters that work for some sample types but fail on others, so levelling often remains a manual, subjective bottleneck. Here, we present two U-Net models developed using machine learning for levelling AFM images without altering the sample topography. MLMask segments features so that they are excluded from conventional plane and line background fits, and MLBackground predicts the noise and artifact background directly, which is then subtracted. Both were trained on 2,001 experimental images from multiple instruments and sample types, using manually levelled images as ground truth. On 164 unseen images, MLMask routines brought 70-80% of images below a mean squared error of 0.1 relative to manual levelling, compared with 60-70% for the best multi-plane method, with a lower mean error (0.1-0.15 vs 0.15-0.3), and both models significantly outperformed fourteen classical routines (p < 0.01). Applied frame by frame, the models process 512x512 pixel HS-AFM movies at 4.7 frames.s-1. We provide afMLevel as an openly-available package for the use of other researchers. By removing the need to choose levelling parameters image by image, this package together with its models and paired training data, provides a foundation for automated AFM analysis pipelines.

biophysics↗

High resolution structure of plant Light-Harvesting Complex II (LHCII) provides insight into lutein conformations and energy quenching

Plant Light Harvesting Complex II (LHCII) is found in the thylakoid membranes of chloroplasts and balances two roles: energy collection for photosynthesis and energy dissipation to prevent photo-damage when there is excessive sunlight. The mechanism for LHCII to switch between two energetic states has been debated but may involve a pH-triggered conformational change. Here we present single-particle cryo-electron microscopy (EM) structures of "light-harvesting" LHCII in detergent at pH 7.5 and pH 4.5. The high resolution (2.48 [A]) maps provide clear placements for all bound pigments, giving high confidence in the models. Surprisingly, we find that there is little conformational change to the polypeptide between these new light harvesting structures and previously published crystals structures, thought to be energy dissipating. The crossing angles of helix A/B and the Lutein 1-Chlorophyll 612 separation distances are similar. This contrasts with other recent analyses of LHCII by single-particle EM that suggested a change to the helix A/B angle and a reduction in Lutein 1-Chlorophyll 612 separation may trigger quenching and a photoprotective state. The high resolution of our structures also allowed us to investigate small conformational changes of the lutein within L1/L2 binding sites of LHCII, revealing rotations and distortions in the pigment that could lead to changes in energy transfer. In addition, we find that low pH causes LHCII to form a destabilised structure where pigment loss from the V1 binding site (usually violaxanthin or zeaxanthin) correlated with a disordered C-terminus, often for just one LHCII monomer with an LHCII trimer. Overall, our findings have important implications for the molecular mechanism of photoprotection.

biochemistry↗

The impact of carotenoid energy levels on the exciton dynamics and singlet-triplet annihilation in the bacterial Light-Harvesting 2 complex

The light-harvesting 2 (LH2) complex of purple phototrophic bacteria plays a critical role in absorbing solar energy and distributing excitation energy. Exciton dynamics within LH2 complexes are controlled by the structural arrangement and energy levels of the bacteriochlorophyll (BChl) and carotenoid (Car) pigments. However, there is still debate over the competing light-harvesting versus energy-dissipation pathways. In this work, we compared five variants of the LH2 complex from genetically modified strains of Rhodobacter sphaeroides, all containing the same BChls but different Cars with increasing conjugation: zeta-carotene (N=7; LH2Zeta), neurosporene (N=9; LH2Neu), spheroidene (N=10; LH2Spher), lycopene (N=11; LH2Lyco), and spirilloxanthin (N=13; LH2Spir). Absorption measurements confirmed that Car excited state energy decreased with increasing conjugation. Similarly, fluorescence spectra showed that the B850 BChl emission peak had an increasing red shift from LH2Zeta[->](LH2Neu/LH2Spher)[->]LH2Lyco[->]LH2Spir. In contrast, time-resolved fluorescence and ultrafast transient absorption (fs-TA) revealed similar excited state lifetimes ([~]1 ns) for all complexes except LH2Spir ([~]0.7 ns). From fs-TA analysis, an additional [~]7 ps non-radiative dissipation step from B850 BChl was observed for LH2Zeta. Further, singlet-singlet and singlet-triplet annihilation studies showed a [~]50% average fluorescence lifetime reduction in LH2Zeta at high laser power and high repetition rate, compared to [~]10-15% reductions in LH2Neu/LH2Spher/LH2Lyco and minimal lifetime change in LH2Spir. In LH2Zeta, the fastest decay component (<50 ps) became prominent at high repetition rates, consistent with strong singlet-triplet annihilation. Nanosecond TA measurements revealed long-lived (>40 s) BChl triplet states in LH2Zeta and signs of damage caused by singlet oxygen, whereas other LH2s showed faster triplet quenching ([~]18 ns) by Cars. These findings highlight a key design principle of LH2 complexes: the Car triplet energy must be significantly lower than the BChl triplet energy to efficiently quench BChl triplets that otherwise act as potent "trap states" causing exciton annihilation in laser-based experiments or photo-damage in native membranes.

biophysics↗

Evidence for a transfer-to-trap mechanism of fluorophore concentration quenching in lipid bilayers

It is important to understand the behaviours of fluorescent molecules because, firstly, they are often utilized as probes in biophysical experiments and, secondly, they are crucial cofactors in biological processes such as photosynthesis. A phenomenon called fluorescence quenching occurs when fluorophores are present at high concentrations but the mechanisms for quenching are debated. Here, we used a technique called in-membrane electrophoresis to generate concentration gradients of fluorophores within a supported lipid bilayer (SLB), across which quenching was expected to occur. Fluorescence lifetime imaging microscopy (FLIM) provides images where the fluorescence intensity in each pixel is correlated to fluorescence lifetime: the intensity provides information about the location and concentration of fluorophores and the lifetime reveals the occurrence of energy-dissipative processes. FLIM was used to compare the quenching behaviour of three commonly-used fluorophores: Texas Red (TR), nitrobenzoaxadiazole (NBD) and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY). FLIM images provided evidence of quenching in regions where the fluorophores accumulated but the degree of quenching varied between the different fluorophores. The relationship between quenching and concentration was quantified and the critical radius for trap formation, representing the relative quenching strength, was calculated as 2.70, 2.02 and 1.14 nm, for BODIPY, TR and NBD, respectively. The experimental data supports the theory that quenching takes place via a transfer-to-trap mechanism which proposes, firstly, that excitation energy is transferred between fluorophores and may reach a trap site resulting in immediate energy dissipation and, secondly, that trap sites are formed in a concentration-dependent manner. Some previous work suggested that quenching occurs only when fluorophores aggregate, or form long-lived dimers, but our data and this theory argues that traps may be statistical pairs of fluorophores that exist only transiently. Our findings should inspire future work to assess whether these traps can be charge-transfer states, excited state dimers or something else.

biophysics↗

Enhancing the spectral range of plant and bacterial Light-Harvesting pigment-protein complexes with various synthetic chromophores incorporated into lipid vesicles

The Light-Harvesting (LH) pigment-protein complexes found in photosynthetic organisms have the role of absorbing solar energy with high efficiency and transferring it to reaction centre complexes. LH complexes contain a suite of pigments that each absorb light at specific wavelengths, however, the natural combinations of pigments within any one protein complex do not cover the full range of solar radiation. Here, we provide an in-depth comparison of the relative effectiveness of five different organic "dye" molecules (Texas Red, ATTO, Cy7, Dil, DiR) for enhancing the absorption range of two different LH membrane protein complexes (the major LHCII from plants and LH2 from purple phototrophic bacteria). Proteoliposomes were self-assembled from defined mixtures of lipids, proteins and dye molecules and their optical properties were quantified by absorption and fluorescence spectroscopy. Both lipid-linked dyes and alternative lipophilic dyes were found to be effective excitation energy donors to LH protein complexes, without the need for direct chemical or generic modification of the proteins. The Forster theory parameters (e.g., spectral overlap) were compared between each donor-acceptor combination and found to be good predictors of an effective dye-protein combination. At the highest dye-to-protein ratios tested (over 20:1), the effective absorption strength integrated over the full spectral range was increased to ~180% of its natural level for both LH complexes. Lipophilic dyes could be inserted into pre-formed membranes although their effectiveness was found to depend upon favourable physicochemical interactions. Finally, we demonstrated that these dyes can also be effective at increasing the spectral range of surface-supported models of photosynthetic membranes, using fluorescence microscopy. The results of this work provide insight into the utility of self-assembled lipid membranes and the great flexibility of LH complexes for interacting with different dyes.

biophysics↗

Understanding the photophysics and structural organization of photosynthetic proteins using model lipid membranes assembled from natural plant thylakoids

The light-harvesting (LH) biomembranes from photosynthetic organisms perform solar energy absorption and transfer with high efficiency. There is great interest in the nanoscale biophysics of photosynthesis, however, natural membranes are complex and highly curved so can be challenging to study. Here we present model photosynthetic "hybrid membranes" assembled from a combination of natural LH membranes and synthetic lipids deposited into a patterned polymerized lipid template on glass. This arrangement offers many advantages over previous model systems including: a sufficiently complex mixture of natural proteins to mimic the biological processes, a modular self-assembly mechanism, and a stabilizing template promoting the formation of supported lipid bilayers from complex natural membranes with high protein content (that would not otherwise form). These hybrid membranes can be used as a platform to delineate the complex relationship between LH energy pathways and membrane organization. Atomic force microscopy and fluorescence lifetime microscopy revealed that hybrid membranes have an elongated fluorescence lifetime ([~]4 ns) compared to native membranes ([~]0.5 ns), a direct consequence of reduced protein density and an uncoupling of protein-protein interactions. We observed the real time self-assembly and migration of LH proteins from natural membrane extracts into the hybrid membranes and monitored the photophysical state of the membranes at each stage. Finally, experiments utilizing our hybrid membranes suggest that assays currently used in the photosynthesis community to test the electron transfer activity of Photosystem II may have non-specific interactions with other proteins, implying that new methods are needed for reliable quantification of electron transfers in photosynthesis.

biophysics↗

Proteoliposomes as energy transferring nanomaterials: enhancing the spectral range of light-harvesting proteins using lipid-linked chromophores

Biology provides a suite of optically-active nanomaterials in the form of \"light harvesting\" protein-chlorophyll complexes, however, these have drawbacks including their limited spectral range. We report the generation of model lipid membranes (proteoliposomes) incorporating the photosynthetic protein Light-Harvesting Complex II (LHCII) and lipid-tethered Texas Red (TR) chromophores that act as a \"bio-hybrid\" energy transferring nanomaterial. The effective spectral range of the protein is enhanced due to highly efficient energy transfer from the TR chromophores (up to 94%), producing a marked increase in LHCII fluorescence (up to 3x). Our self-assembly procedure offers excellent modularity allowing the incorporation of a range of concentrations of energy donors (TR) and acceptors (LHCII), allowing the energy transfer efficiency (ETE) and LHCII fluorescence to be tuned as desired. Fluorescence Lifetime Imaging Microscopy (FLIM) provides single-proteoliposome-level quantification of ETE, revealing distributions within the population and proving that functionality is maintained on a surface. Our membrane-based system acts as a controllable light harvesting nanomaterial with potential applications as thin films in photo-active devices.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=92 SRC=\"FIGDIR/small/609255v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (32K):\norg.highwire.dtl.DTLVardef@e663f3org.highwire.dtl.DTLVardef@1abfa78org.highwire.dtl.DTLVardef@1c90d5aorg.highwire.dtl.DTLVardef@8b99db_HPS_FORMAT_FIGEXP M_FIG Table of Contents Figure C_FIG

biophysics↗