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According to the basic principles of chemiosmosis (ref 29), electron flow through the respiratory chain is coupled to the translocation of protons from the matrix side of the inner membrane to the outer side.
On the mitochondrial matrix side of the carrier most residues of the three matrix α-helices that are in the interface with the transmembrane α-helical bundle are important for function.
For example, the original stress state was 0.78% in compressive; after the NiO/LDC (Ce0.55La0.45O3 − δ) anode deposited on the LSCM buffer, the anode side of LSCM revealed the compressive strain with 3.34% and the matrix side of LSCM revealed the tensile strain with 10.65%.
The arms of the y-shaped monomers lie within and perpendicular to the lipid bilayer protruding approximately 25 A on the matrix side of the membrane.
Decoration of the exposed matrix side of vesicle crystals with antisubunit IV antibody fragments indicates that subunit IV lies along the a-crystal axis roughly 20 A from the center of the dimer.
Located on the matrix side of the inner mitochondrial membrane, Ndi1 is a 513aa, 56kDa protein containing a noncovalently bound FAD.
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Tantalum is observed to partition preferentially to the γ′-precipitate phase, and suppresses the mobility of Ni in the γ-matrix sufficiently to cause an accumulation of Ni on the γ-matrix side of the γ′/γ interface.
Subunits IV and Va were placed into a protruding density on the matrix side so that the concave side of the protein, which forms the dimer interface in 3D crystals, faced outwards.
Our analysis indicates that the uniform and hydrostatic stress field inside the inclusion as well as the constant hoop stress along the entire inclusion matrix interface (on the matrix side) are independent of the action of the point moment.
Additionally, at the matrix side, the flexible region of COX7A (subunit of CIV) contact with both UQCRC1 and UQCR11 (subunits of CIII).
Inner membrane proteins are also inserted from the matrix side by the action of the Oxa1 proteins.
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