Toward a new picture of the living plasma membrane

Our understanding of the plasma membrane structure has undergone a major change since the proposal of the fluid mosaic model of Singer and Nicholson in the 1970s. In this model, the membrane, composed of over thousand lipid and protein species, is organized as a well‐equilibrated two‐dimensional fluid. Here, the distribution of lipids is largely expected to reflect a multicomponent system, and proteins are expected to be surrounded by an annulus of specialized lipid species. With the recognition that a multicomponent lipid membrane is capable of phase segregation, the membrane is expected to appear as patchwork quilt pattern of membrane domains. However, the constituents of a living membrane are far from being well equilibrated. The living cell membrane actively maintains a trans‐bilayer asymmetry of composition, and its constituents are subject to a number of dynamic processes due to synthesis, lipid transfer as well as membrane traffic and turnover. Moreover, membrane constituents engage with the dynamic cytoskeleton of a living cell, and are both passively as well as actively manipulated by this engagement. The extracellular matrix and associated elements also interact with membrane proteins contributing to another layer of interaction. At the nano‐ and mesoscale, the organization of lipids and proteins emerge from these encounters, as well as from protein–protein, protein–lipid, and lipid–lipid interactions in the membrane. New methods to study the organization of membrane components at these scales have also been developed, and provide an opportunity to synthesize a new picture of the living cell surface as an active membrane composite.     

Untangling the taxonomic ambiguities of the spotted seerfish Scomberomorus guttatus with the description of a new species from India

Scomberomorus guttatus has been subjected to a series of synonym assignations over the years. Its taxonomy has been mired with ambiguities due to the greater-than-average morphological variations observed in samples from different regions. An integrated taxonomic revision with molecular support indicated that the species that was thought to be a single entity, in reality, is a complex of three distinct species. They are morphologically distinct with respect to the body depth and elongation, cephalic morphometry, and meristic characteristics. Otolith morphometry and phylogenetic evidence further established the taxonomic divergence within the spotted seerfish complex. The phylogenetic characteristic as indicated by the mitochondrial Cytochrome c Oxidase subunit I (COI) sequence unveiled that S. guttatus had a high intraspecific divergence of 11.1% from its two identical congeners and a divergence of 2.34% between the congeners, indicating scope for categorizing them as separate species. Based on the morphological and molecular evidence, S. guttatus is redescribed; the senior synonym Scomberomorus leopardus is resurrected as a valid species; and a new species Scomberomorus avirostrus n. sp. is described with keys for species distinction.     

Isolation,Synthesis and AChE Inhibitory Potential of Some Novel Cinnamyl Esters of Taraxerol,the Major Metabolite of the Mangrove Bruguiera cylindrica

Systematic chemical screening of the leaves of Bruguiera cylindrica, the tree mangrove of Rhizophoraceae family, afforded five single and pure compounds. The structures of the isolated compounds were established by their spectroscopic data as taraxerol ( 1 ), 3β‐(E)‐coumaroyltaraxerol ( 2 ), 3β‐(Z)‐coumaroyltaraxerol ( 3 ), β‐sitosterol ( 4 ), and eicosanol ( 5 ). In view of significant accumulation and interesting biological activities, taraxerol ( 1 ) was chemically transformed to synthesize a series of ten cinnamyl esters in very good to excellent yields. The synthesized analogues along with the parent compound were evaluated for their AChE inhibitory potential, BBB permeability and cytotoxicity against Neuro 2A cell line. Among the tested samples, compound 9 showed promising AChE inhibition with significantly low IC₅₀ values, low cytotoxicity and high BBB permeability. Hence, compound 9 can be considered as a lead molecule for further development as potent AChE inhibitor.