Mysteries of the collagen triple helix

被引:0
|
作者
Bachinger, Hans Peter [1 ,2 ]
Boudko, Sergei P. [3 ,4 ,5 ]
机构
[1] Shriners Hosp Children, Res Dept, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97229 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Div Nephrol, Nashville, TN USA
[4] Vanderbilt Univ, Vanderbilt Ctr Matrix Biol, Med Ctr, Nashville, TN USA
[5] Vanderbilt Univ, Dept Biochem, Nashville, TN USA
关键词
Collagen triple helix; Folding; Trimerization domain; peptidyl-prolyl cis-trans isomerase (PPIase); Molecular ensemble of collagen biosynthesis; pharmacological chaperone; CIS-TRANS-ISOMERIZATION; FK506-BINDING PROTEIN; III PROCOLLAGEN; PEPTIDE-BONDS; NC2; DOMAIN; TRIMERIZATION; IV; HYSTERESIS; ISOMERASE; CHAPERONE;
D O I
10.1016/j.matbio.2025.02.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The collagen triple helix is one of the structurally simplest protein motifs that still holds a lot of secrets. The GlyX-Y repeat is a business card of collagens, where Gly is required for the tight packing of three helices into a superhelix and X and Y residues are important for stabilizing the triple helix and communicating with the world. On its way to a functional molecule, collagen sequences undergo unique post-translational modifications inside and outside of the cell. Moreover, folding and secretion of collagens require specific proteins and mechanisms. Cracking the collagen triple helix codes opens up opportunities for curing associated diseases and developing new biomaterials. Here, we summarized my journey through some mysteries of the collagen triple helix and point out key unaddressed questions and problems for other researchers to pursue.
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页数:7
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