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Published byMagdalen Howard Modified over 6 years ago
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Lecture 13 Post-transcriptional processing of mRNA Membranes again
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Post-transcriptional Gene control (Chapter 8)
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hnRNP proteins coat the RNA immediately upon its exiting from RNA polymerase
Human hnRNP A1 (red) and C (green) proteins distribute differently in the cytoplasm of a heterokaryon
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Consensus sequence around splice sites
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The chemistry of RNA splicing
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The mutated mismatched A is in this position
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Exonic splicer enhancers
Average length of intron ~3500 bases exons are ~ 150 bases long SR proteins (serine-arginine rich) interact with exonic splicing enhancers, mediate cooperative binding U1 snRNP to a true 5’ splice site. This helps forming cross-exon recognition complex
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Membranes and lipids Wikipedia
Functions: compartmentation, maintain internal milieu, transport, energy transduction, signal propagation, cell-cell communication, ingestion, secretion, sensation, storage etc.
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Membranes are self-organizing structures
Staining artifact due to binding of a contrasting agent (Uranyl or Osmium) to the polar headgroups Membranes are self-organizing structures
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PE, PC: zwitterions, PS:anionic PS and PE have H-bonding capacity
(Phospholipids) glycerol PE, PC: zwitterions, PS:anionic PS and PE have H-bonding capacity
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Phosphatidic acid (PA)
Phosphatidyl glycerol (PG)
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Phosphatidylinositol
Phosphatidylinositol diphosphate (PIP2)
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Critical trans double bond
sphingosine ceramide NH
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Cholesterol
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Lipids have their spontaneous curvature
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Micelles, Liposomes and Lamellar phases
SDS
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Lipid Bilayers are dynamic
distributions of phosphate and carbonyl groups and lateral pressure profiles From S. Feller
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Distribution of groups along the z-axis
from S. White
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