Author:
O’Brien Jonathon J.,Narayan Vikram,Wong Yao,Seitzer Phillip,Sandoval Celeste M.,Haste Nicole,Smith Megan,Rad Ramin,Gaun Aleksandr,Baker Adam,Kukurugya Matthew,Martin-McNulty Baby,Zhang Chunlian,Kolumam Ganesh,Sidrauski Carmela,Jojic Vladimir,McAllister Fiona,Bennett Bryson,Buffenstein Rochelle
Abstract
AbstractIsotopic labeling with deuterium oxide (D2O) is a common technique for estimating in vivo protein turnover, but its use has been limited by two long-standing problems: (1) identifying non-monoisotopic peptides; and (2) estimating protein turnover rates in the presence of dynamic amino acid enrichment. In this paper, we present a novel experimental and analytical framework for solving these two problems. Peptides with high probabilities of labeling in many amino acids present fragmentation spectra that frequently do not match the theoretical spectra used in standard identification algorithms. We resolve this difficulty using a modified search algorithm we call Conditional Ion Distribution Search (CIDS). Increased identifications from CIDS along with direct measurement of amino acid enrichment and statistical modeling that accounts for heterogeneous information across peptides, dramatically improves the accuracy and precision of half-life estimates. We benchmark the approach in cells, where near-complete labeling is possible, and conduct an in vivo experiment revealing, for the first time, differences in protein turnover between mice and naked mole-rats commensurate with their disparate longevity.
Publisher
Cold Spring Harbor Laboratory
Cited by
6 articles.
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