Professor Jane A. Grasby (she/her)
School of Mathematical and Physical Sciences
School Director of One University
Professor of Biological Chemistry
+44 114 222 9478
Full contact details
School of Mathematical and Physical Sciences
Dainton Building
13 Brook Hill
ºù«Ӱҵ
S3 7HF
- Profile
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Professor Grasby obtained her BSc in Chemistry from the University of Birmingham in 1988. After obtaining her PhD in Biochemistry from the University of Southampton in 1992, she became a Research Fellow at the Laboratory of Molecular Biology in Cambridge.
In 1994 she was appointed to a Lectureship at the University of ºù«Ӱҵ, where she was promoted to Senior Lecturer in 1999, Reader in 2002 and a Personal Chair in 2013. Prof. Grasby has acted as Chair of the Faculty of Science Equality Diversity Committee.
- Research interests
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The interactions and reactions of nucleic acids are fundamental to life. Our research has seeks to understand these processes using a range of techniques including chemical synthesis of modified nucleic acids, molecular biology, enzymology, biophysics (fluorescence, CD and NMR spectroscopies) and X-ray crystallography. We are particularly interested in the catalysis of reactions of nucleic acids (RNA and DNA) and most recently in the question of how structure, but not sequence, specific nucleases achieve specificity in nucleic acid hydrolysis.
Flap endonucleases (FENs, shown below human FEN1 (hFEN1) with DNA substrate) have been the focus of much of our recent work. FENs are a vital component of the lagging strand DNA replication apparatus in all organisms and also play role in DNA repair in eukaryotes. FENs remove 5’-single-stranded protrusions to double-stranded DNA known as flaps, formed as a result of DNA polymerase strand displacement synthesis.
In humans FENs have to carry out approximately 50 million phosphate diester hydrolyses to allow replication of a single cell. FEN1 is the prototypical member of a superfamily of structure-specific 5’-nucleases whose differing activities span all the major DNA metabolic pathways.
Each of the 5’-nucleases acts on a different substrates. Recently, we have been trying to understand both common features of 5’-nucleases and the specialised mechanisms they use to carry out their extraordinary feats of molecular recognition. We have a learnt that the single stranded DNA flap is threaded through a hole in the protein known as the helical arch.
This threading mechanism allows the enzyme to act on discontinuous flap DNAs that have free 5’-ends, but importantly not at single-strand double-strand junctions in DNA that are continuous. The DNA becomes threaded through the arch while this region of the protein is disordered. Forming the helical structure delivers key amino acid residues to the active site to catalyse phosphodiester hydrolysis.
- Publications
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Journal articles
- . Journal of the American Chemical Society, 145(2), 953-959.
- . Biochemistry, 57(50), 6838-6847.
- . Nucleic Acids Research, 46(15), 7858-7872.
- . Nucleic Acids Research, 46(11), 5618-5633.
- . Nature Communications.
- . Biochemistry, 56(29), 3704-3707.
- . Nature Communications, 8.
- . Nature Chemical Biology, 12, 815-821.
- . Journal of Biological Chemistry, 291(15), 8258-8268.
- . Nucleic Acids Res, 42(7), 4577-4589.
- . J. Biol. Chem., 288, 34239-34248.
- . Nucleic Acids Res, 41(21), 9839-9847.
- , 301-326.
- . Proc Natl Acad Sci U S A, 109(46), 18755-18760.
- . Chem Commun (Camb), 48(91), 11214-11216.
- . Chem Commun (Camb), 48(71), 8895-8897.
- . Nucleic Acids Res, 40(10), 4507-4519.
- . Trends in Biochemical Sciences, 37(2), 74-84.
- . Trends Biochem Sci, 37(2), 74-84.
- . J Biol Chem, 286(35), 30878-30887.
- . Cell, 145(2), 198-211.
- . Biochemistry, 49(37), 8085-8093.
- . Biochem Soc Trans, 38(2), 433-437.
- . J Biol Chem, 284(33), 22184-22194.
- . J Biol Chem, 283(42), 28741-28746.
- . J Mol Biol, 371(1), 34-48.
- . J Mol Biol, 368(2), 421-433.
- . Org Biomol Chem, 2(14), 2103-2112.
- . Nucleic Acids Res, 32(21), 6240-6250.
- . Nucleic Acids Res, 32(4), 1591-1601.
- . J Biol Chem, 278(45), 44001-44008.
- . EMBO J, 22(5), 995-1004.
- . J Mol Biol, 324(2), 215-226.
- . Eur J Biochem, 269(22), 5492-5501.
- . J Mol Biol, 320(5), 1025-1035.
- . Proc Natl Acad Sci U S A, 99(13), 8542-8547.
- . Eur J Biochem, 269(5), 1525-1533.
- . RNA, 8(2), 247-251.
- . Nucleic Acids Res, 29(9), 1898-1905.
- . Nucleic Acids Res, 29(7), 1565-1573.
- . Biochemical Society Transactions, 29(1), A30-A30.
- Novel syntheses of (Z)-alkene and alkane base-modified nucleosides. TETRAHEDRON LETT, 41(2), 267-270.
- . J Biol Chem, 274(25), 17711-17717.
- . J Mol Biol, 288(5), 853-866.
- . Nucleic Acids Res, 27(3), 730-735.
- Synthesis and incorporation of a novel nucleoside phosphoramidite linker into oligonucleotides. CHEMISTRY OF NUCLEIC ACID COMPONENTS, 2, 119-123.
- The synthesis of modified 5-(aminoalkyl)- and 5-(aminoalkenyl)uridine 5 '-triphosphates. CHEMISTRY OF NUCLEIC ACID COMPONENTS, 2, 35-38.
- A novel solid support for synthesis of 2 ',3 '-cyclic phosphate terminated oligonucleotides. TETRAHEDRON LETT, 39(43), 7975-7978.
- Incorporation of methylated pyrimidine analogues into RNA. TETRAHEDRON LETT, 39(28), 5093-5096.
- . Nucleic Acids Res, 25(19), 3760-3766.
- . J Biol Chem, 271(15), 8855-8862.
- Mechanistic studies of the hairpin ribozyme. COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 61, S268-S270.
- Synthesis of uridine analogues to probe the functional group requirements of the hairpin ribozyme. COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 61, S280-S282.
- . Biochemistry, 34(12), 4068-4076.
- SYNTHESIS AND APPLICATIONS OF OLIGORIBONUCLEOTIDES CONTAINING N-4-METHYLCYTIDINE. NUCLEOSIDES & NUCLEOTIDES, 14(3-5), 1129-1132.
- SYNTHETIC RIBONUCLEOTIDE ANALOGS FOR RNA STRUCTURE-FUNCTION STUDIES. NUCLEOSIDES & NUCLEOTIDES, 14(3-5), 1133-1144.
- APPLICATIONS OF SYNTHETIC OLIGORIBONUCLEOTIDE ANALOGS IN STUDIES OF RNA STRUCTURE AND FUNCTION. P INDIAN AS-CHEM SCI, 106(5), 1003-1022.
- . Nucleic Acids Res, 22(13), 2592-2600.
- . Biochimie, 76(12), 1223-1234.
- . Nucleic Acids Res, 21(19), 4444-4450.
- . Collection of Czechoslovak Chemical Communications, 58(s1), 154-157.
- 7-DEAZAADENOSINE - OLIGORIBONUCLEOTIDE BUILDING-BLOCK SYNTHESIS AND AUTOCATALYTIC HYDROLYSIS OF BASE-MODIFIED HAMMERHEAD RIBOZYMES. HELV CHIM ACTA, 76(5), 1809-1820.
- . Biochemistry, 31(34), 7855-7861.
- . ChemInform, 24(48), no-no.
Chapters
- The hairpin ribozyme In Meunier B (Ed.) (pp. 295-306).
- , Organophosphorus Chemistry (pp. 161-230). Royal Society of Chemistry
- , Organophosphorus Chemistry (pp. 170-236). Royal Society of Chemistry
- , Organophosphorus Chemistry (pp. 177-263). Royal Society of Chemistry
- , Organophosphorus Chemistry (pp. 196-264). Royal Society of Chemistry
Conference proceedings papers
- The Catalytic Cycle of hFEN1 Requires Protein and DNA Conformational Changes, but Are They Rate-Limiting?. PROTEIN SCIENCE, Vol. 24 (pp 147-147)
- . Biophysical Journal, Vol. 106(2) (pp 230a-230a)
- Investigations into substrate analogues for Fen-1. Chemistry of Nucleic Acid Components, Vol. 7 (pp 347-350)
- Kinetic studies of the Neurospora vs ribozyme. CHEMISTRY OF NUCLEIC ACID COMPONENTS, Vol. 5 (pp 352-355)
- Investigating catalytic RNA molecules. CHEMISTRY OF NUCLEIC ACID COMPONENTS, Vol. 5 (pp 231-240)
- Synthesis of polyamine-uridine conjugates by derivatisation at the 5-position. CHEMISTRY OF NUCLEIC ACID COMPONENTS, Vol. 5 (pp 241-244)
- Mechanistic studies of a 5 ' nuclease from T5 bacteriophage. CHEMISTRY OF NUCLEIC ACID COMPONENTS, Vol. 2 (pp 161-167)
- Functional group mutagenesis of the hairpin ribozyme. CHEMISTRY OF NUCLEIC ACID COMPONENTS, Vol. 2 (pp 306-309)
Website content
- Teaching interests
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Organic Chemistry; Biological Chemistry
- Teaching activities
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Undergraduate and postgraduate taught modules
- Carbonyl Compounds and Carboxylic Acids (Level 1)
This lecture course introduces methods for the synthesis of carboxylic acid derivatives and discusses their reactions. - Chemistry in a Sustainable Future (Level 1)
- Introduction to Chemical Biology & Medicinal Chemistry (Level 3)
This course introduces the basic principles of chemical biology and medicinal chemistry - Skills for Success (Level 3; course Leader)
The Skills for Success Project aims to ensure that students identify and develop skills that will be of use to them in life, future study and employment and provide a basis from which they can undertake further training of a professional nature.
Support Teaching:
- Tutorials: Level 1 General Chemistry.
- Level 3 Literature Review
Laboratory Teaching:
- Level 4 Research Project
- Carbonyl Compounds and Carboxylic Acids (Level 1)