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  2. Beryllium fluoride - Wikipedia

    en.wikipedia.org/wiki/Beryllium_fluoride

    Beryllium fluoride has distinctive optical properties. In the form of fluoroberyllate glass, it has the lowest refractive index for a solid at room temperature of 1.275. Its dispersive power is the lowest for a solid at 0.0093, and the nonlinear coefficient is also the lowest at 2 × 10 −14.

  3. Chemical glycosylation - Wikipedia

    en.wikipedia.org/wiki/Chemical_glycosylation

    A chemical glycosylation reaction involves the coupling of a glycosyl donor, to a glycosyl acceptor forming a glycoside. [ 1 ] [ 2 ] [ 3 ] If both the donor and acceptor are sugars, then the product is an oligosaccharide .

  4. Glycosylation - Wikipedia

    en.wikipedia.org/wiki/Glycosylation

    It is a spontaneous reaction and a type of post-translational modification of proteins meaning it alters their structure and biological activity. It is the covalent attachment between the carbonil group of a reducing sugar (mainly glucose and fructose) and the amino acid side chain of the protein. In this process the intervention of an enzyme ...

  5. Tetrafluoroberyllate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroberyllate

    The Be–F bond length is between 145 and 153 pm.The beryllium is sp 3 hybridized, leading to a longer bond than in BeF 2, where beryllium is sp hybridized. [11] In trifluoroberyllates, there are actually BeF 4 tetrahedra arranged in a triangle, so that three fluorine atoms are shared on two tetrahedra each, resulting in a formula of Be 3 F 9.

  6. Glycation - Wikipedia

    en.wikipedia.org/wiki/Glycation

    Glycation (non-enzymatic glycosylation) is the covalent attachment of a sugar to a protein, lipid or nucleic acid molecule. [1] Typical sugars that participate in glycation are glucose , fructose , and their derivatives.

  7. Glycoprotein - Wikipedia

    en.wikipedia.org/wiki/Glycoprotein

    The most common method of glycosylation of N-linked glycoproteins is through the reaction between a protected glycan and a protected Asparagine. [5] Similarly, an O-linked glycoprotein can be formed through the addition of a glycosyl donor with a protected Serine or Threonine. [5] These two methods are examples of natural linkage. [5]

  8. N-linked glycosylation - Wikipedia

    en.wikipedia.org/wiki/N-linked_glycosylation

    The different types of lipid-linked oligosaccharide (LLO) precursor produced in different organisms.. N-linked glycosylation is the attachment of an oligosaccharide, a carbohydrate consisting of several sugar molecules, sometimes also referred to as glycan, to a nitrogen atom (the amide nitrogen of an asparagine (Asn) residue of a protein), in a process called N-glycosylation, studied in ...

  9. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak bonding between the two fluorine atoms. [9] This is a result of the relatively large electron and internuclear repulsions, combined with a relatively small overlap of bonding orbitals arising ...