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1.
Int J Inj Contr Saf Promot ; 31(3): 521-533, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38753177

RESUMEN

This study examines the impact of urban form and street infrastructure on pedestrian safety in Atlanta, Georgia, and Boston, Massachusetts. With a significant rise in pedestrian fatalities over the past decade, understanding how cities' built environments influence safety is critical. We conducted geospatial analyses and statistical tests, revealing unique patterns in each city. Atlanta's sprawling, motorist-oriented layout is associated with increased pedestrian accidents, particularly at crosswalks, due to limited land use diversity, arterial roads, and streets with high speed limits and multiple lanes. In contrast, Boston's compact, pedestrian-oriented design leads to improved safety, featuring safer pedestrian crossings, greater land use diversity, reduced arterial roads and lower speed limits on single-lane streets. This study also highlights the importance of diverse urban forms and pedestrian infrastructure in shaping pedestrian safety. While population density and land use diversity impact accident rates, the presence of crosswalks and street configurations play crucial roles. Our findings underscore the urgency for urban planners to prioritize pedestrian safety through targeted interventions, such as enhancing crosswalks, reducing speed limits and promoting mixed land use. Future research should explore additional variables, alternative modelling techniques and non-linear approaches to gain a more comprehensive understanding of these complex relationships.


Asunto(s)
Accidentes de Tránsito , Entorno Construido , Planificación Ambiental , Peatones , Humanos , Accidentes de Tránsito/prevención & control , Accidentes de Tránsito/mortalidad , Georgia , Boston , Seguridad , Ciudades , Caminata
2.
Biochim Biophys Acta Bioenerg ; 1864(2): 148945, 2023 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-36442511

RESUMEN

Knowledge about the exact abundance and ratio of photosynthetic protein complexes in thylakoid membranes is central to understanding structure-function relationships in energy conversion. Recent modeling approaches for studying light harvesting and electron transport reactions rely on quantitative information on the constituent complexes in thylakoid membranes. Over the last decades several quantitative methods have been established and refined, enabling precise stoichiometric information on the five main energy-converting building blocks in the thylakoid membrane: Light-harvesting complex II (LHCII), Photosystem II (PSII), Photosystem I (PSI), cytochrome b6f complex (cyt b6f complex), and ATPase. This paper summarizes a few quantitative spectroscopic and biochemical methods that are currently available for quantification of plant thylakoid protein complexes. Two new methods are presented for quantification of LHCII and the cyt b6f complex, which agree well with established methods. In addition, recent improvements in mass spectrometry (MS) allow deeper compositional information on thylakoid membranes. The comparison between mass spectrometric and more classical protein quantification methods shows similar quantities of complexes, confirming the potential of thylakoid protein complex quantification by MS. The quantitative information on PSII, PSI, and LHCII reveal that about one third of LHCII must be associated with PSI for a balanced light energy absorption by the two photosystems.


Asunto(s)
Complejo de Citocromo b6f , Tilacoides , Tilacoides/metabolismo , Complejo de Citocromo b6f/metabolismo , Citocromos b/metabolismo , Complejos de Proteína Captadores de Luz/metabolismo , Complejo de Proteína del Fotosistema I/metabolismo , Proteínas de Plantas/metabolismo
3.
Methods Mol Biol ; 1770: 305-316, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29978410

RESUMEN

The biological role of lipids goes far beyond the formation of a structural membrane bilayer platform for membrane proteins and controlling fluxes across the membranes. For example, in photosynthetic thylakoid membranes, lipids occupy well-defined binding niches within protein complexes and determine the structural organization of membrane proteins and their function by controlling generic physicochemical membrane properties. In this chapter, two-dimensional thin-layer chromatography (2D TLC) and gas chromatography (GC) techniques are presented for quantitative analysis of lipid classes and fatty acids in thylakoid membranes. In addition, lipid extraction methods from isolated thylakoid membranes and leaves are described together with a procedure for derivatization of fatty acids to fatty acid methyl esters (FAME) that is required for GC analysis.


Asunto(s)
Membrana Celular/metabolismo , Metabolismo de los Lípidos , Fotosíntesis , Cromatografía de Gases , Cromatografía en Capa Delgada , Lípidos/química , Lípidos/aislamiento & purificación , Hojas de la Planta
4.
J Biol Chem ; 290(22): 14091-106, 2015 May 29.
Artículo en Inglés | MEDLINE | ID: mdl-25897076

RESUMEN

The structural organization of proteins in biological membranes can affect their function. Photosynthetic thylakoid membranes in chloroplasts have the remarkable ability to change their supramolecular organization between disordered and semicrystalline states. Although the change to the semicrystalline state is known to be triggered by abiotic factors, the functional significance of this protein organization has not yet been understood. Taking advantage of an Arabidopsis thaliana fatty acid desaturase mutant (fad5) that constitutively forms semicrystalline arrays, we systematically test the functional implications of protein crystals in photosynthetic membranes. Here, we show that the change into an ordered state facilitates molecular diffusion of photosynthetic components in crowded thylakoid membranes. The increased mobility of small lipophilic molecules like plastoquinone and xanthophylls has implications for diffusion-dependent electron transport and photoprotective energy-dependent quenching. The mobility of the large photosystem II supercomplexes, however, is impaired, leading to retarded repair of damaged proteins. Our results demonstrate that supramolecular changes into more ordered states have differing impacts on photosynthesis that favor either diffusion-dependent electron transport and photoprotection or protein repair processes, thus fine-tuning the photosynthetic energy conversion.


Asunto(s)
Arabidopsis/metabolismo , Complejo de Proteína del Fotosistema II/metabolismo , Tilacoides/metabolismo , Cristalización , Transporte de Electrón , Electrones , Recuperación de Fluorescencia tras Fotoblanqueo , Microscopía Electrónica , Mutación , Oxígeno/metabolismo , Fotosíntesis , Espectrometría de Fluorescencia , Espectrofotometría
5.
Plant Physiol ; 161(1): 497-507, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23148078

RESUMEN

The photosynthetic performance of plants is crucially dependent on the mobility of the molecular complexes that catalyze the conversion of sunlight to metabolic energy equivalents in the thylakoid membrane network inside chloroplasts. The role of the extensive folding of thylakoid membranes leading to structural differentiation into stacked grana regions and unstacked stroma lamellae for diffusion-based processes of the photosynthetic machinery is poorly understood. This study examines, to our knowledge for the first time, the mobility of photosynthetic pigment-protein complexes in unstacked thylakoid regions in the C3 plant Arabidopsis (Arabidopsis thaliana) and agranal bundle sheath chloroplasts of the C4 plants sorghum (Sorghum bicolor) and maize (Zea mays) by the fluorescence recovery after photobleaching technique. In unstacked thylakoid membranes, more than 50% of the protein complexes are mobile, whereas this number drops to about 20% in stacked grana regions. The higher molecular mobility in unstacked thylakoid regions is explained by a lower protein-packing density compared with stacked grana regions. It is postulated that thylakoid membrane stacking to form grana leads to protein crowding that impedes lateral diffusion processes but is required for efficient light harvesting of the modularly organized photosystem II and its light-harvesting antenna system. In contrast, the arrangement of the photosystem I light-harvesting complex I in separate units in unstacked thylakoid membranes does not require dense protein packing, which is advantageous for protein diffusion.


Asunto(s)
Arabidopsis/metabolismo , Fotosíntesis , Complejo de Proteína del Fotosistema I/metabolismo , Complejo de Proteína del Fotosistema II/metabolismo , Tilacoides/metabolismo , Arabidopsis/fisiología , Clorofila/metabolismo , Clorofila A , Difusión , Electroforesis en Gel de Poliacrilamida , Recuperación de Fluorescencia tras Fotoblanqueo , Luz , Lípidos de la Membrana/metabolismo , Células del Mesófilo/metabolismo , Microscopía Confocal , Hojas de la Planta/metabolismo , Hojas de la Planta/fisiología , Transporte de Proteínas , Protoplastos/metabolismo , Sorghum/metabolismo , Sorghum/fisiología , Especificidad de la Especie , Tilacoides/fisiología , Zea mays/metabolismo , Zea mays/fisiología
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