Download - RNA catalysis

RNA catalysisUnderstand the basics of RNA/DNA catalysts - what functional groups used for catalysis? structures formed?

Know about transesterification & cleavage reactions

Know four types of natural catalytic RNAs (group I introns, group II introns, RNase P, small self-cleaving), what reactions they perform, know basics of their secondary and tertiary structure, requirements for cofactors/metals/proteins/ATP

Know details of glmS ribozyme self-cleavage

Understand use of ribozymes as therapeutics

In vitro selection - understand the process

Know some of the ribozymes and deoxyribozymes that have been discovered using in vitro selection

Outline

• RNA transesterification

• Naturally occurring catalysts

• Catalytic functions

• Catalytic mechanisms

RNA transesterification• Exchange one phosphate ester for another

• Free energy change is minimal (reversible)

RNA transesterification• Nucleophile can be either the adjacent 2´ hydroxyl or

another ester

• Referred to as hydrolysis when water serves as the nucleophile

RNA transesterification• Nucleophilic attack on the phosphorus center leads to a

penta-coordinate intermediate

• Ester opposite from the nucleophile serves as the leaving group (in-line attack)

General mechanisms• Substrate positioning

• Transition state stabilization

• Acid-base catalysis

• Metal ion catalysis

RNA Catalysts

Naturally occurring catalysts• RNA cleavage

glmS ribozyme (crystal structure)hammerhead ribozyme (crystal structure)hairpin ribozyme (crystal structure)Varkud satellite (VS) ribozyme (partial NMR structure)hepatitis delta virus (HDV) ribozyme (crystal structure)M1 RNA (RNase P) (partial crystal structure)

• RNA splicing

group I introns (crystal structure)group II introns (crystal structure)*** U2-U6 snRNA (spliceosome) (partial NMR structure) ***

• Peptide bond formation

ribosome (crystal structure)

Small self-cleaving ribozymes• Hammerhead, hairpin, VS, HDV ribozymes

• Derivative of viral, viroid, or satellite RNAs

• Involved in RNA processing during rolling circle replication

• RNA transesterification via 2´ hydroxyl

• Reversible: cleavage and ligation (excepting HDV)

Hammerhead ribozyme• Three-stem junction with conserved loop regions

• Coaxial stacking of stems II and III through extended stem II structure containing canonical Watson-Crick and non-canonical base pairs

• Metal-ion catalysis

Hammerhead ribozyme

• In nature is self-cleaving (not a true enzyme)

• Can be manipulated to function as a true catalyst

• Biotechnological and potential therapeutic applications for target RNA cleavage

Hammerhead ribozyme• Separation of catalytic and substrate strands

• Strand with hairpin is the enzyme

• Single strand is substrate

• KM = 40nM; kcat = ~1 min-1;kcat/KM = ~107 M -1 min -1 (catalytic efficiency)

• Compare to protein enzymes?

RNA Catalysts • basics of catalytic reactions (cleavage)

RNase AProtein enzyme

Hammerheadribozyme

Hairpin ribozyme• In nature is part of a four-stem junction

• Ribozyme consists of two stems with internal loops

• Stems align side-by-side with 180 degree bend in the junction (hence ‘hairpin’)

• Internal loops interact to form active site

Hairpin ribozyme

• Crystal structure reveals interactions between stems

• Nucleobases position and activate scissile phosphodiester linkage

• Combination of transition state stabilization and acid-base catalysis?

HDV ribozyme

• Genomic and antigenomic ribozymes

• Nested pseudoknot structure

• Very stable

• Cleaves off 5´ leader sequence

HDV ribozyme

HDV ribozyme• Active site positions an

important cytidine near the scissile phosphodiester bond

RNase P• True enzyme

• Cleaves tRNA precursor to generate the mature 5´ end

• Composed of M1 RNA and C5 protein (14 kD)

• RNA is large and structurally complex

• Protein improves turnover

• Hydrolysis

Group I introns• Large family of self-splicing introns usually

residing in rRNA and tRNA

• Two step reaction mechanism

Group I intron structure

• Crystal structure of ‘trapped’ ribozyme before second transesterification reaction

• Metal ion catalysis

Group I intron structure

Ribose zipper

P1

J8/7

Group II introns

Group II introns

• Usually found in organelles (e.g. plant chloroplasts, mitochondria)

• mechanism proceeds through a branched lariat intermediate structure which is produced by the attack of a 2’-OH of an internal A on the phosphodiester of the 5’-splice site

• proteins thought to stabilize structure but not necessary for catalysis

• no ATP or exogenous G needed

Summary of splicing reactions

The ribosome is a ribozyme• Ribosome is 2/3 RNA and 1/3 protein by mass

• Crystal structures prove that RNA is responsible for decoding and for peptide bond formation

Peptidyl transferase

• Crystal structure of 50S subunit shows no protein within 20 Å of peptidyl transferase center

• Closest component to aa-tRNA is adenosine 2451 in 23S rRNA

• Proposed acid-base mechanism for peptide bond formation

• Recent evidence showssubstrate positioningaccounts for catalysis

Glucosamine 6-phosphate riboswitch/ribozyme

• Glucosamine-6-phosphate (GlcN6P)-dependent self-cleaving ribozyme

• Regulates biosynthesis of amino sugars used in bacterial cell wall synthesis

glmS is a metabolite-responsive ribozyme

M

Effects of [glcN6P] on the rate constant.

Optimization of catalysis by the glmS ribozyme

Glucosamine 6-phosphate ribozyme self-cleavageRNA transesterification

Glucosamine 6-phosphate ribozyme self-cleavageRNA transesterification

Might glucosamine 6-phosphate serve as the general acid-base (coenzyme) for self-cleavage?

Ribozyme exhibits self-cleavage activity in

TRIS buffer in the absence of ligand

McCarthy, T.J., Plog, M.A., Floy, S.A., Jansen, J.A., Soukup, J.K. & Soukup, G.A. "Ligand requirements for glmS ribozyme self-cleavage." Chemistry & Biology 12:1-6 (2005).

Ligand specificity -importance of amine functionality


Table 1. Kinetic parameters for the glmS ribozyme in the absence or presence of 10 mM

GlcN6P or various analogs.

ligand kobs (min-1) apparent KD (mM) rate enhancement

GlcN6P 1.1 0.03 110,000

GlcN 3.0 x 10-2 ≥5 3,000

Serinol 7.5 x 10-3 ≥5 750

TRIS 1.3 x 10-3 ≥25 130

– ~10-5 – –

Observed rate constants and apparent binding of ligand analogs



• GlcN and serinol are lower affinity ligands

• Apparent pKa for ligand-dependent self-cleavage approximates the solution pKa of ligand

• Suggest the amine functionality of the ligand functions as a general acid/base in catalysis

pH-reactivity profiles

RNA/DNA Catalysts RNA/DNA catalysis & evolution

• in vitro selection

RNA/DNA Catalysts RNA/DNA catalysis & evolution

• increasing numbers of examples of reactions catalyzed by nucleic acidsTable 1. Catalytic RNA and DNA molecules isolated from in vitro selection1

Catalytic Nucleic Acid Reaction Catalyzed or Activity

RNA Aminoacyl esteraseRNA DNA CleavageRNA RNA CleavageRNA RNA LigationRNA Isomerization of a bridged biphenylRNA Self-phosphorylationRNA Amide bond cleavageRNA AminoacylationRNA AlkylationRNA 5'-5' RNA ligationRNA Acyl transferase (ester and amide bond formation)RNA Porphyrin metalation with Cu2+ (heme biosynthesis)RNA Sulfur alkylationRNA 5'-self-cappingRNA Carbon-carbon bond formation (Diels-Alder cycloaddition)RNA Amide bond formationRNA Peptide bond formationRNA Ester transferase

DNA RNA cleavageDNA DNA ligationDNA Porphyrin metalation with Cu2+ (heme biosynthesis)DNA Cleave phosphoramidate bondsDNA DNA cleavageDNA Self-phosphorylationDNA 5'-self-capping

1Ref. 44. This list is only an overview and does not include all nucleic acid catalystsdiscovered to date.

DNA Catalysts

Download - RNA catalysis

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