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Biology subjects

Chalmers, G.

Publications and source records attributed to Chalmers, G..

2 recordsLinked to original sources

Triceps Surae Muscle Ia Proprioceptive Weighting During Quiet Stance with Vision Occlusion

Visual, vestibular, proprioceptive and cutaneous sensory information is important for posture control during quiet stance. When the reliability of one source of sensory information used to detect self-motion for posture control is reduced, there may be a reweighting of inputs within and/or across the remaining sensory systems determining self-motion for postural control. Muscle vibration, which creates an illusion of muscle stretch and a compensatory movement to shorten the vibrated muscle, may be used to determine the weighting of muscle spindle Ia proprioception for posture control. The objective of this study was to determine the effect of vision occlusion on triceps surae muscle Ia proprioceptive weighting for postural control during quiet stance, utilizing 80 Hz muscle vibration and a quantitative measure of the bodys anterior to posterior ground center of pressure response to triceps surae muscle vibration in freely standing subjects. Subjects (N = 41; mean(standard deviation), 19.6(2.0) years) were examined as they stood with eyes open or eyes closed. Ground center of pressure was measured during quiet standing with, and without, bilateral vibration of the triceps surae muscles. The mean backward center of pressure shift induced by triceps surae vibration was significantly greater during the eyes closed condition compared to eyes open (eyes closed: -4.93(1.62) centimeters; eyes open: -3.21(1.33) centimeters; p = 6.85E-10; Cohens d = 1.29). Thirty-seven subjects increased, and two subjects decreased, their vibration induced center of pressure backward shift in the eyes closed condition compared to eyes open, although the magnitude of the change varied. Results support the idea that for most subjects, during an eyes closed stance there is an increased triceps surae muscle Ia proprioceptive weighting for postural control, due to the need for posture control to depend more on non-visual feedback.

neuroscience↗

A common binding motif in the ET domain of BRD3 forms polymorphic structural interfaces with host and viral proteins

The extra-terminal (ET) domain of BRD3 is conserved among BET proteins (BRD2, BRD3, BRD4), interacting with multiple host and viral protein-protein networks. Solution NMR structures of complexes formed between BRD3-ET domain with either the 79-residue murine leukemia virus integrase (IN) C-terminal domain (IN329-408), or its 22-residue IN tail peptide (TP) (IN386-407) alone, reveal similar intermolecular three-stranded {beta}-sheet formation. 15N relaxation studies reveal a 10-residue linker region (IN379-388) tethering the SH3 domain (IN329-378) to the ET-binding motif (IN389-405)-ET complex. This linker has restricted flexibility, impacting its potential range of orientations in the IN - nucleosome complex. The complex of the ET-binding peptide of host NSD3 protein (NSD3148-184) and BRD3-ET domain includes a similar three-stranded {beta}-sheet interaction, but the orientation of the {beta}-hairpin is flipped compared to the two IN : ET complexes. These studies expand our understanding of molecular recognition polymorphism in complexes of ET-binding motifs with viral and host proteins. HighlightsO_LIThe BRD3 ET domain binds to key peptide motifs of diverse host and viral proteins. C_LIO_LIThese complexes reveal conformational plasticity in molecular recognition. C_LIO_LINMR studies demonstrate restricted interdomain motion in the IN CTD / ET complex. C_LIO_LIA cost-effective approach is described for producing isotopically-labeled peptides. C_LI Etoc BlurbWe address structurally how the MLV Integrase (IN) usurps the host function of the BET protein through comparative studies of the IN : Brd3 ET complex with that of the host NSD3. MLV integration and thus its pathogenesis is driven through protein interactions of the IN : BET family.

microbiology↗