Amit Choudhary Lab Publications - The Amit Choudhary Lab

44.

CRISPR-based therapeutics: Current challenges and future applications

Under revision

43.

harnessing reaction-based probes to preferentially target pancreatic beta-cells and beta-like cells

Under revision

42.

A general approach to identify miniature and cell-permeable anti-cRISPRs

To be submitted

41.

Core Commitments For Field Trials Of Gene Drive Organisms.

K.C. Long, L. Alphey, G. J. Annas, C. S. Bloss, K. J. Campbell, J. Champer, C-H Chen, A. Choudhary, G. M. Church, J. P. Collins, K. L. Cooper, J. A. Delborne, O. R. Edwards, C. I. Emerson, K. Esvelt, S. W. Evans, R. M. Friedman, V. M. Gantz, F. Goud, S. Hartley, E. Heitman, J. Hemingway, H. Kanuka, J. Kuzma, J. V. Lavery, Y. Lee, M. Lorenzen, J. E. Lunshof, J. M. Marshall, P. W. Messer, C. Montell, K. A. Oye, M. J. Palmer, P. A. Papthanos, P. N. Paradkar, A. J. Piaggio, J. L. Rasgon, G. Rasic, L. Rudenko, J. R. Saah, M. J. Scott, J. T. Sutton, A. E. Vorsino, O. S. Akbari
Science. 2020, 370, 1417.

Highlighed in: EurekAlert, Phys.org, Science Daily

40.

Chemical And Optical Control Of CRISPR-Associated Nucleases.

A. E. Modell, S. U. Siriwardena, V. M. Shoba, X. Li, A. Choudhary.
Current Opinion in Chemical Biology. In press

39.

A 3D culture platform enables development of zinc-based prodrugs for targeted proliferation of beta cells.

K. Yang, M. Lee, P. A. Jones, S. S. Liu, A. Zhou, J. Xu, V. Sreekanth, J. L. Y. Wu, L.Vo, E. A. Lee, R. Pop, Y. Lee, B. K. Wagner, D. A. Melton, A. Choudhary*, J. M. Karp*
Science Advances. In Press

38.

A chemogenetic system demonstrates that Cas9 longevity impacts genome editing outcome.

V. Sreekanth, Q. Zhou, P. Kokkonda, H. Bermudez-Cabrera, D. Lim, B. Law, B. Holmes, S. Chaudhary, R. Pergu, B. Leger, J. A. Walker, D. Gifford, R. Sherwood, A. Choudhary. ACS Central Science. In Press

37.

Engineering designer beta cells with a CRISPR-Cas9 conjugation platform.

D. Lim, V. Sreekanth, K. J. Cox, B. K. Law, B. K. Wagner, J. M. Karp, and A. Choudhary.
Nature Communications 2020, 11, 4043.

Highlighted in: Faculty of 1000, Nature Bioengineering Blog

36.

Phosphorylation-inducing chimeric small molecules.

S. U. Siriwardena, D. N. P. M. Godage, V. M. Shoba, S. Lai, M. Shi, P. Wu, S. K. Chaudhary, S. L. Schreiber, and A. Choudhary
Journal of the American Chemical Society 2020, 142, 14052 – 14057
Highlighted in: BIOCENTURY, Faculty of 1000

35.

A Jumbo phage forms a nucleus-like compartment to evade bacterial defense systems.

A. E. Modell, S.U. Siriwardena and A. Choudhary
Biochemistry 2020, 59, 1869-1870.

34.

A small molecule control of super-Mendelian inheritance in gene drives.

V. L. D. Amo, B. S. Leger, K. J. Cox, S. Gill, A. L. Bishop, G. D. Scanlon, J. A. Walker, V. M. Gantz, A. Choudhary
Cell Reports 2020, 31,107841.

Highlighted in: GEN

33.

Native zinc mediates selective and traceless release of small molecules in beta cells.

M. Lee, B. Maji, D. Manna, S. Kahraman, R. M. Elgamal, J. Small, P. Kokkonda, A. Vetere, J. M. Goldberg, S. J. Lippard, R. N. Kulkarni, B. K. Wagner and A. Choudhary
Journal of the American Chemical Society 2020, 142, 6477 – 6482.

32.

A high-throughput platform to identify small-molecule inhibitors of CRISPR-Cas9

B. Maji, S. A. Gangopadhyay, M. Lee, M. Shi, P. Wu, R. Heler, B. Mok, D. Lim, S. U. Siriwardena, B. Paul, V. Dančík, A. Vetere, M. F. Mesleh, L. A. Marraffini, D. R. Liu, P. A. Clemons, B. K. Wagner and A. Choudhary
Cell 2019, 177, 1067-1079.

Highlighted in: Cell Press, Nature, Nature Methods, Nature Rev Drug Discovery, Broad Institute, Harvard Gazette, NewScientist, GEN, GenomeWeb, Phys.org, ScienceDaily, MIT Tech Review, In the Pipeline & several others.

31.

Precision control of CRISPR-Cas9 using light and small molecules.

S. A. Gangopadhyay, K. J. Cox, D. Manna, D. Lim, B. Maji, Q. Zhou, A. Choudhary
Biochemistry 2019, 58, 234-244.

30.

A singular system for dose and spatiotemporal control of CRISPR-Cas9

D. Manna, B. Maji, S. A. Gangopadhyay, K. J. Cox, Q. Zhou, B. K. Law, R. Mazitschek, A. Choudhary
Angewandte Chemie International Edition 2019, 58, 6285-6289.

Highlighted in: BioSpace

29.

A universal method for sensitive and cell-free detection of CRISPR-associated nucleases.

K. J. Cox, H. K. K. Subramanian, C. C. Samaniego, E. Franco and A. Choudhary
Chemical Science 2019, 10, 2653 – 2662.

28.

Book Chapter: Kinase Inhibitor Drugs

P. Wu and A. Choudhary
© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA.

27.

Special Issue on the Chemical Biology of CRISPR

A. G. Weidmann and A. Choudhary.
ACS Chemical Biology 2018, 13, 283–284.
Highlighted in: IGTRCN

26.

Growth and stress response mechanisms underlying post-feeding regenerative organ growth in the Burmese python.

A. L. Andrew, B, W, Perry, D. C. Card, D. R. Schield, R. P, Ruggiero, Suzanne E. McGaugh, A. Choudhary, S. M. Secor, T. A. Castoe
BMC Genomics 2017, 18, 338.

25.

Multidimensional chemogenic control of CRISPR-Cas9.

B. Maji, C. L. Moore, B. Zetsche, S. E. Volz, F. Zhang, M. D. Shoulders, A. Choudhary
Nature Chemical Biology 2017, 13, 9-11.
Highlighted in: News & Views

24.

Prolyl 4-Hydroxylase: Substrate Isosteres in Which an (E)- or (Z)-Alkene Replaces the Prolyl Peptide Bond.

J. D. Vasta, A. Choudhary, K. H. Jensen, N. A. McGrath and R. T. Raines
Biochemistry 2016, 56, 219–227.

23.

Kinase-Independent Small-Molecule Inhibition of JAK-STAT Signaling.

D. H-C. Chou,§ A. Vetere, § A. Choudhary, § S. S. Scully, M. Schenone, A. Tang, R. Gomez, S. M. Burns, M. Lundh, T. Vital, E. Comer, P. W. Faloon, V. Dančík, C. Ciarlo, J. Paulk, M. Dai, C. Reddy, H. Sun, M. Young, N. Donato, J. Jaffe, P. A. Clemons, M. Palmer, S. A. Carr, S. L. Schreiber and B. K. Wagner
Journal of the American Chemical Society 2015, 137, 7929 – 7934.

22.

4‐ketoproline: An electrophilic proline analog for bioconjugation

A. Choudhary, K. J. Kamer, M. D. Shoulders, R. T. Raines.
Peptide Science 2015, 104, 110-115.

21.

Targeting the pancreatic β-cell to treat diabetes

A. Vetere, A. Choudhary, S. M. Burns & B. K. Wagner.
Nature Reviews Drug Discovery 2014, 13, 278–289.

20.

Quantitative-Proteomic Comparison of Alpha and Beta Cells to Uncover Novel Targets for Lineage Reprogramming.

A. Choudhary, K. H. He , P. Mertins, N. D. Udeshi, V. Dančík, D. F. Yadlin, S. Kubicek, P. A. Clemons, S. L. Schreiber, S. A. Carr, B. K. Wagner.
PloS one 2014, 9, e95194.

19.

n→ π* interactions engender chirality in carbonyl groups.

A. Choudhary, R. W. Newberry and R. T. Raines
Organic Letters 2014, 16, 3421 – 3423.

18.

An n→ π* interaction reduces the electrophilicity of the acceptor carbonyl group.

A. Choudhary, C. G. Fry, K. J. Kamer, and R. T. Raines
Chemical Communications 2013, 49, 8166 – 8168.

17.

Pyramidalization of a carbonyl C atom in (2S)-N-(selenoacetyl) proline methyl ester.

I. A. Guzei, A. Choudhary, and R. T. Raines.
Acta Crystallographica Section E: Structure Reports Online 2013. 69, 805-806.

16.

Intimate interactions with carbonyl groups: dipole–dipole or n→ π*?

K. J. Kamer, A. Choudhary and R.T. Raines
The Journal of Organic Chemistry 2012, 78, 2099 – 2103.

15.

Synthesis of 5-Fluoro-and 5-Hydroxymethanoprolines via Lithiation of N-BOC-methanopyrrolidines. Constrained Cγ-Exo and Cγ-Endo Flp and Hyp Conformer Mimics.

G. R. Krow, M. D. Shoulders, R. Edupuganti, D. Gandla, F. Yu, P. E. Sonnet, M. Sender, A. Choudhary, C. DeBrosse, C. W. Ross III, P. Carroll and R. T. Raines
The Journal of Organic Chemistry 2012, 77, 5331 – 5344.

14.

A conserved interaction with the chromophore of fluorescent proteins.

A. Choudhary, K. J. Kamer and R. T Raines
Protein Science 2011, 21, 171-177.

13.

An evaluation of peptide‐bond isosteres.

A. Choudhary and R. T. Raines.
ChemBioChem 2011, 12, 1801-1807.

12.

An n→ π* interaction in aspirin: Implications for structure and reactivity.

A. Choudhary, K. J. Kamer and R. T. Raines.
The Journal of Organic Chemistry 2011, 76, 7933 – 7937.

11.

Signature of n→ π* interactions in α‐helices.

A. Choudhary and R. T. Raines.
Protein Science 2011, 20, 1077-1081.

10.

Synthesis of conformationally constrained 5-fluoro-and 5-hydroxymethanopyrrolidines. Ring-puckered mimics of gauche-and anti-3-fluoro-and 3-hydroxypyrrolidines.

G. R. Krow, R. Edupuganti, D. Gandla, F. Yu, M. Sender, P. E. Sonnet, M. J. Zdilla, C. DeBrosse, K. C. Cannon, C. W. Ross III and A. Choudhary, M. D. Shoulders and R. T. Raines.
The Journal of Organic Chemistry 2011, 76, 3626 – 3634.

9.

Quantum mechanical origin of the conformational preferences of 4-thiaproline and its S-oxides.

A. Choudhary, K. H. Pua and R. T. Raines.
Amino Acids 2011, 41, 181-186.

8.

The aberrance of the 4S diastereomer of 4-hydroxyproline.

M. D. Shoulders, F. W. Kotch, A. Choudhary, I. A. Guzei and R. T. Raines
Journal of the American Chemical Society 2010, 132, 10857 – 10865.

7.

A Stereoelectronic Effect in Prebiotic Nucleotide Synthesis.

A. Choudhary, K. J. Kamer, M. W. Powner, J. D. Sutherland and R. T. Raines
ACS Chemical Biology 2010, 5, 655-657.

6.

n→ π* interactions in proteins.

G. J. Bartlett, A. Choudhary, R. T. Raines and D .N. Woolfson
Nature Chemical Biology 2010, 6, 615-620.

5.

n → π* Interaction and n)(π Pauli Repulsion Are Antagonistic for Protein Stability.

C. E. Jakobsche, A. Choudhary, S. J. Miller and R. T. Raines
Journal of the American Chemical Society 2010, 132, 6651 – 6653.

4.

Modulation of an n→ π* interaction with α-fluoro groups.

A. Choudhary, C. G. Fry and R. T. Raines
ARKIVOC: free online journal of organic chemistry/Arkat-USA Inc. 2010, 8, 251-262.

3.

5(6)-anti-Substituted-2-azabicyclo[2.1.1]hexanes: A Nucleophilic Displacement Route.

G. R. Krow, R. Edupuganti, D. Gandla, A. Choudhary, G. Lin, P. E. Sonnet, C. DeBrosse, C. W. Ross, K. C. Cannon and R. T. Raines
The Journal of Organic Chemistry 2009, 74, 8232 – 8242.

2.

Nature of Amide Carbonyl−Carbonyl Interactions in Proteins.

A. Choudhary, D. Gandla, G. R. Krow and R. T. Raines
Journal of the American Chemical Society 2009, 131, 7244 – 7246.

1.

Stereoselective synthesis of (−)-microcarpalide.

K. R. Prasad, K. Penchalaiah, A. Choudhary and P. Anbarasan
Tetrahedron Letters 2007, 48, 309-311.