Anti-KRAS binding proteins

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Mar. 30, 2019, is named 2019-03-30_01223-0016-00US_SequenceListing.txt and is 145 kilobytes in size.

TECHNICAL FIELD

The present disclosure provides human antibodies that bind KRAS, KRAS-binding fragments and derivatives of such antibodies, KRAS-binding polypeptides comprising such fragments, and conjugates thereof.

BACKGROUND OF THE INVENTION

The KRAS gene (also known as V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog), encodes a 2.1-kDa small protein that is activated transiently in response to extracellular stimuli or signals such as growth factors, cytokines, and hormones via cell surface receptors. The RAS proteins are guanine nucleotide binding molecules that play key roles in signal transduction as molecular switches, mediated through two switch regions displaying conformational differences between active (GTP bound) and inactive (GDP bound) states. Most of the RAS effectors bind to these RAS switch regions.

The protein product of the KRAS gene performs an essential function in normal tissue signaling, where the mutation of a KRAS gene is an essential step in the development of many cancers. The RAS oncogenes (1-IRAS, NRAS and KRAS) comprise the most frequently mutated class of oncogenes in human cancers (33%), stimulating intensive effort in developing anti-RAS inhibitors for cancer treatment. RAS is an important target in cell transformation, being involved in cell proliferation and differentiation and cell survival through activation of PI3K. Aside from a few rare exceptions, mutationally activated Ras proteins found in human cancers result predominantly from one of three single point mutations at residues G12, G13, or Q61. Oncogenic substitution of G12 or G13 leads to constitutive activation of Ras by creating steric hindrance that prevents the formation of van der Waals interactions between Ras and RasGAPS (Scheffzek et al (1997) Science 277, 333-338).

RAS-based therapies have been challenging (see, for example, Cardinale et al. (2003) Eur. J. Biochem. 270:3389), especially given the intracellular nature of the target. Tanaka et al. (2007) EMBO J. 26:3250 describes a single antibody domain that targeted the interaction of signal transduction proteins with RAS, and was able to impact protein-protein interactions. There remains an unmet need for novel agents that block aberrant KRAS function for cancer treatments, particularly therapies directed to intracellular targets such as KRAS.

SUMMARY OF THE INVENTION

The invention provides antibodies that specifically bind to KRAS, including human KRAS.

In one aspect, the invention features an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising a heavy chain CDR set (CDR1, CDR2, and CDR3) of amino acid sequences selected from the group consisting of SEQ ID Nos. 75, 76 and 77; SEQ ID Nos. 81, 82 and 83; SEQ ID Nos. 87, 88 and 89; SEQ ID Nos. 93, 94 and 95; SEQ ID Nos. 99, 100 and 101; SEQ ID Nos. 105, 106 and 107; SEQ ID Nos. 111, 112 and 113; SEQ ID Nos. 117, 118 and 119; SEQ ID Nos. 123, 124 and 125; SEQ ID Nos. 129, 130 and 131; SEQ ID Nos. 135, 136 and 137; SEQ ID Nos. 141, 142 and 143; SEQ ID Nos. 147, 148 and 149; SEQ ID Nos. 153, 154 and 155; SEQ ID Nos. 159, 160, 161; SEQ ID Nos. 165, 166 and 167; SEQ ID Nos. 171, 172 and 173; SEQ ID Nos. 177, 178 and 179; SEQ ID Nos. 183, 184 and 185; SEQ ID Nos. 189, 190 and 191; SEQ ID Nos. 195, 196 and 197; SEQ ID Nos. 201, 202 and 203; SEQ ID Nos. 207, 208 and 209; SEQ ID Nos. 213, 214 and 215; SEQ ID Nos. 219, 220 and 221; SEQ ID Nos. 225, 226 and 227; SEQ ID Nos. 231, 232 and 233; SEQ ID Nos. 237, 238 and 239; SEQ ID Nos. 243, 244 and 245; SEQ ID Nos. 249, 250 and 251; SEQ ID Nos. 255, 256 and 257; SEQ ID Nos. 261, 262 and 263; SEQ ID Nos. 267, 268 and 269; SEQ ID Nos. 273, 274 and 275; SEQ ID Nos. 279, 280 and 281; SEQ ID Nos. 285, 286 and 287; SEQ ID Nos. 291, 292 and 293; and SEQ ID Nos. 299, 300 and 301; and a light chain variable domain comprising a light chain CDR set (CDR1, CDR2, and CDR3) of amino acid sequences selected from the group consisting of SEQ ID Nos. 78, 79 and 80; SEQ ID Nos. 84, 85 and 86; SEQ ID Nos. 90, 91 and 92; SEQ ID Nos. 96, 97 and 98; SEQ ID Nos. 102, 103 and 104; SEQ ID Nos. 108, 109 and 110; SEQ ID Nos. 114, 115 and 116; SEQ ID Nos. 120, 121 and 122; SEQ ID Nos. 126, 127 and 128; SEQ ID Nos. 132, 133 and 134; SEQ ID Nos. 138, 139 and 140; SEQ ID Nos. 144, 145 and 146; SEQ ID Nos. 150, 151 and 152; SEQ ID Nos. 156, 157 and 158; SEQ ID Nos. 162, 163 and 164; SEQ ID Nos. 168, 169 and 170; SEQ ID Nos. 174, 175 and 176; SEQ ID Nos. 180, 181 and 182; SEQ ID Nos. 186, 187 and 188; SEQ ID Nos. 192, 193 and 194; SEQ ID Nos. 198, 199 and 200; SEQ ID Nos. 204, 205 and 206; SEQ ID Nos. 210, 211 and 212; SEQ ID Nos. 216, 217 and 218; SEQ ID Nos. 222, 223 and 224; SEQ ID Nos. 228, 229 and 230; SEQ ID Nos. 234, 235 and 236; SEQ ID Nos. 240, 241 and 242; SEQ ID Nos. 246, 247 and 248; SEQ ID Nos. 252, 253 and 254; SEQ ID Nos. 258, 259 and 260; SEQ ID Nos. 264, 265 and 266; SEQ ID Nos. 270, 271 and 272; 276, 277 and 278; SEQ ID Nos. 282, 283 and 284; SEQ ID Nos. 288, 289 and 290; SEQ ID Nos. 294, 295 and 296 and SEQ ID Nos. 302, 303 and 304. In one embodiment, the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 297 and comprising the heavy chain CDR set of SEQ ID Nos: 299, 300 and 301. In another embodiment, the light chain variable domain is selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; and a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296; and a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 298 and comprising the light chain CDR set of SEQ ID Nos: 302, 303 and 304. In another embodiment, the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 297 and comprising the heavy chain CDR set of SEQ ID Nos: 299, 300 and 301. In one embodiment of any one of the above aspects or embodiments, the light chain variable domain is selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; a light chain variable domain comprising an amino acid sequence that is at least 96% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296; and a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 298 and comprising the light chain CDR set of SEQ ID Nos: 302, 303 and 304. In another embodiment, the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 297 and comprising the heavy chain CDR set of SEQ ID Nos: 299, 300 and 301. In one embodiment of any one of the above aspects or embodiments, the light chain variable domain is selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; a light chain variable domain comprising an amino acid sequence that is at least 97% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296; and a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 298 and comprising the light chain CDR set of SEQ ID Nos: 302, 303 and 304. In another embodiment of any one of the above aspects or embodiments, the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 297 and comprising the heavy chain CDR set of SEQ ID Nos: 299, 300 and 301. In another embodiment of any one of the above aspects or embodiments, the light chain variable domain is selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296; and a light chain variable domain comprising an amino acid sequence that is at least 98% identical to SEQ ID NO: 298 and comprising the light chain CDR set of SEQ ID Nos: 302, 303 and 304. In another embodiment of any one of the above aspects or embodiments, the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 297 and comprising the heavy chain CDR set of SEQ ID Nos: 299, 300 and 301. In another embodiment of any one of the above aspects or embodiments, the light chain variable domain is selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296; and a light chain variable domain comprising an amino acid sequence that is at least 99% identical to SEQ ID NO: 298 and comprising the light chain CDR set of SEQ ID Nos: 302, 303 and 304.

In one aspect, the invention features an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising amino acid sequences of a heavy chain CDR set and a light chain variable domain comprising amino acid sequences of a light chain CDR set, wherein the heavy chain CDR set and the light chain CDR set are selected from the group consisting of a heavy chain variable domain CDR set of SEQ ID Nos: 75, 76 and 77 and a light chain variable domain CDR set of 78, 79 and 80; a heavy chain variable domain CDR set of SEQ ID Nos: 81, 82 and 83 and a light chain variable domain CDR set of 84, 85 and 86; a heavy chain variable domain CDR set of SEQ ID Nos: 87, 88 and 89 and a light chain variable domain CDR set of 90, 91 and 92; a heavy chain variable domain CDR set of SEQ ID Nos: 93, 94 and 95 and a light chain variable domain CDR set of 96, 97 and 98; a heavy chain variable domain CDR set of SEQ ID Nos: 99, 100 and 101 and a light chain variable domain CDR set of 102, 103 and 104; a heavy chain variable domain CDR set of SEQ ID Nos: 105, 106 and 107 and a light chain variable domain CDR set of 108, 109 and 110; a heavy chain variable domain CDR set of SEQ ID Nos: 111, 112 and 113 and a light chain variable domain CDR set of 114, 115 and 116; a heavy chain variable domain CDR set of SEQ ID Nos: 117, 118 and 119 and a light chain variable domain CDR set of 120, 121 and 122; a heavy chain variable domain CDR set of SEQ ID Nos: 123, 124 and 125 and a light chain variable domain CDR set of 126, 127 and 128; a heavy chain variable domain CDR set of SEQ ID Nos: 129, 130 and 131 and a light chain variable domain CDR set of 132, 133 and 134; a heavy chain variable domain CDR set of SEQ ID Nos: 135, 136 and 137 and a light chain variable domain CDR set of 138, 139 and 140; a heavy chain variable domain CDR set of SEQ ID Nos: 141, 142 and 143 and a light chain variable domain CDR set of 144, 145 and 146; a heavy chain variable domain CDR set of SEQ ID Nos: 147, 148 and 149 and a light chain variable domain CDR set of 150, 151 and 152; a heavy chain variable domain CDR set of SEQ ID Nos: 153, 154 and 155 and a light chain variable domain CDR set of 156, 157 and 158; a heavy chain variable domain CDR set of SEQ ID Nos: 159, 160 and 161 and a light chain variable domain CDR set of 162, 163 and 164; a heavy chain variable domain CDR set of SEQ ID Nos: 165, 166 and 167 and a light chain variable domain CDR set of 168, 169 and 170; a heavy chain variable domain CDR set of SEQ ID Nos: 171, 172 and 173 and a light chain variable domain CDR set of 174, 175 and 176; a heavy chain variable domain CDR set of SEQ ID Nos: 177, 178 and 179 and a light chain variable domain CDR set of 180, 181 and 182; a heavy chain variable domain CDR set of SEQ ID Nos: 183, 184 and 185 and a light chain variable domain CDR set of 186, 187 and 188; a heavy chain variable domain CDR set of SEQ ID Nos: 189, 190 and 191 and a light chain variable domain CDR set of 192, 193 and 194; a heavy chain variable domain CDR set of SEQ ID Nos: 195, 196 and 197 and a light chain variable domain CDR set of 198, 199 and 200; a heavy chain variable domain CDR set of SEQ ID Nos: 201, 202 and 203 and a light chain variable domain CDR set of 204, 205 and 206; a heavy chain variable domain CDR set of SEQ ID Nos: 207, 208 and 209 and a light chain variable domain CDR set of 210, 211 and 212; a heavy chain variable domain CDR set of SEQ ID Nos: 213, 1214 and 215 and a light chain variable domain CDR set of 216, 217 and 218; a heavy chain variable domain CDR set of SEQ ID Nos: 219, 220 and 221 and a light chain variable domain CDR set of 222, 223 and 224; a heavy chain variable domain CDR set of SEQ ID Nos: 225, 226 and 227 and a light chain variable domain CDR set of 228, 229 and 230; a heavy chain variable domain CDR set of SEQ ID Nos: 231, 232 and 233 and a light chain variable domain CDR set of 234, 235 and 236; a heavy chain variable domain CDR set of SEQ ID Nos: 237, 238 and 239 and a light chain variable domain CDR set of 240, 241 and 242; a heavy chain variable domain CDR set of SEQ ID Nos: 243, 244 and 245 and a light chain variable domain CDR set of 246, 247 and 248; a heavy chain variable domain CDR set of SEQ ID Nos: 249, 250 and 251 and a light chain variable domain CDR set of 252, 253 and 254; a heavy chain variable domain CDR set of SEQ ID Nos: 255, 256 and 257 and a light chain variable domain CDR set of 258, 259 and 260; a heavy chain variable domain CDR set of SEQ ID Nos: 261, 262 and 263 and a light chain variable domain CDR set of 1264, 265 and 266; a heavy chain variable domain CDR set of SEQ ID Nos: 267, 268 and 269 and a light chain variable domain CDR set of 270, 271 and 272; a heavy chain variable domain CDR set of SEQ ID Nos: 273, 274 and 275 and a light chain variable domain CDR set of 276, 277 and 278; a heavy chain variable domain CDR set of SEQ ID Nos: 279, 280 and 281 and a light chain variable domain CDR set of 282, 283 and 284; a heavy chain variable domain CDR set of SEQ ID Nos: 285, 286 and 287 and a light chain variable domain CDR set of 288, 289 and 290; a heavy chain variable domain CDR set of SEQ ID Nos: 291, 292 and 293 and a light chain variable domain CDR set of 294, 295 and 296; and a heavy chain variable domain CDR set of SEQ ID Nos: 299, 300 and 301 and a light chain variable domain CDR set of 302, 303 and 304.

In one aspect, the invention features an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence that is at least 95% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence that is at least 96% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence that is at least 96% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence that is at least 97% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence that is at least 97% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence that is at least 98% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence that is at least 98% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising an amino acid sequence that is at least 99% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71, SEQ ID NO. 73 and SEQ ID NO. 297; and comprising a light chain variable domain comprising an amino acid sequence that is at least 99% identical to an amino acid sequence selected from the group consisting of: SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72, SEQ ID NO. 74 and SEQ ID NO. 298.

In one aspect, the invention features an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain and a light chain variable domain selected from the group consisting of a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 1 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 2; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 3 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 4; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 5 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 6; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 7 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 8; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 9 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 10; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 11 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 12; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 13 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 14; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 15 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 16; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 17 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 18; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 19 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 20; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 21 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 22; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 23 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 24; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 25 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 26; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 27 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 28; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 29 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 30; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 31 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 32; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 33 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 34; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 35 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 36; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 37 and a light chain variable domain of SEQ ID NO: 38; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 39 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 40; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 41 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 42; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 43 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 44; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 45 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 46; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 47 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 48; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 49 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 50; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 51 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 52; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 53 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 54; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 55 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 56; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 57 and the light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 58; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 59 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 60; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 61 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 62; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 63 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 64; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 65 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 66; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 67 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 68; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 69 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 70; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 71 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 72; a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 73 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 74; and a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 297 and a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO: 298. In one embodiment of any one of the aspects or embodiments above, the antibody has a K_Dof at least 1×10⁻⁶M. In one embodiment of any one of the aspects or embodiments above, the antibody is human. In one embodiment of any one of the aspects or embodiments above, the antibody is an IgG. In another embodiment, the antibody is an IgG1, IgG2, IgG3 or an IgG4 isotype. In one embodiment, the antigen-binding fragment is a Fab fragment or an scFv.

In one aspect, the anti-KRAS antibody, or antigen-binding fragment thereof, of any one of the above aspects or embodiments, is conjugated to an intracellular delivery compound.

In one embodiment, the antibody conjugate is the structure shown in FIG. 2B.

In one embodiment, the antibody conjugate is the structure shown in FIG. 2C.

In one aspect, the invention features a pharmaceutical composition comprising the anti-KRAS antibody, or antibody fragment thereof, of any one of the above aspects or embodiments, and a pharmaceutically acceptable carrier.

In one aspect, the invention features a method for treating a subject having cancer comprising administering an effective amount of the anti-KRAS antibody, or antigen-binding fragment thereof, of any one of the above aspects or embodiments to the subject. In one embodiment, the cancer is a cancer associated with a KRAS mutation. In another embodiment, the KRAS mutation is G12D mutation. In a further embodiment, the cancer is selected from the group consisting of pancreatic cancer, lung cancer, including non-small cell lung cancer, colorectal cancer, prostate cancer, breast cancer, ovarian cancer, head and neck cancer, bladder cancer, melanoma, colorectal cancer, leiomyoma, leiomyosarcoma, glioma, glioblastoma, esophageal cancer, liver cancer, kidney cancer, stomach cancer, colon cancer, cervical cancer, uterine cancer, liver cancer and a hematological cancer.

In another embodiment, the invention features a nucleic acid encoding the antibody or antigen binding fragment of any one of the above aspects or embodiments.

In one embodiment, the invention features a vector comprising the nucleic acid of any one of the aspects or embodiments herein.

In one embodiment, the invention features a host cell comprising the vector of any one of the above aspects or embodiments.

DESCRIPTION OF THE DRAWINGS

FIG. 1 is a graph that shows the binding of fully human anti-KRAS antibody clones 1E3, 4F10 and LN97S to cellular targets in KRAS G12D over-expressing pancreatic tumor cells (ASPC-1). Binding in U2OS human osteosarcoma cells (KRAS wildtype) and A549 human lung adenocarcinoma epithelial cells (KRASG12S expressing cells) were tested as controls. Binding is shown as fold change relative to wild type.

FIG. 2A is a drawing of an exemplary antibody conjugate of the present invention, comprising Formula (I), or a pharmaceutically acceptable salt thereof, wherein each of X, q, Ba, R1, r, t, L, and AT are as defined and described in U.S. Publication No. 20170107289, filed on Oct. 20, 2016; Provisional Appln. No. 62/327,130, filed on Apr. 25, 2016; U.S. Provisional Appln. No. 62/327,132, filed on Apr. 25, 2016; U.S. Provisional Appln. No. 62/327,136, filed on Apr. 25, 2016; and U.S. Provisional Appln. No. 62/327,137, filed on Apr. 25, 2016, each of which are incorporated by reference herein.

FIG. 2B is a drawing of an embodiment of FIG. 2A, showing an exemplary antibody conjugate of the present invention, where the antibody (A_T) is an anti-KRAS antibody and the conjugate is labeled with fluorescein.

FIG. 2C is a drawing of an embodiment of FIG. 2A, showing an exemplary antibody conjugate of the present invention, where the antibody (A_T) is an anti-KRAS antibody, and which is tested in Examples 1-9. In further exemplary embodiments, the antibody (A_T) is anti-KRAS G12D 4F10 antibody. This conjugate is termed Compound 1.

FIG. 3A is a graph that shows the results of a direct ELISA using recombinant KRAS wild type and mutant proteins (wild type, mutant KRAS G12C, and mutant KRAS G12D). The results provided in FIG. 3A show that anti-KRAS G12D antibody 4F10 is specific for KRAS G12D. Anti-human IgG-Fc-HRP was used as a control.

FIG. 3B is a graph that shows the results of high content screening (HCS) confocal microscopy to measure antibody binding to cellular proteins. U2OS are osteosarcoma cells expressing wild-type KRAS. A549 are human lung cancer cells expressing KRAS G12S. ASPC-1 are human pancreatic cancer cells with KRAS G12D mutation.

FIG. 4 is a graph that shows the results of an ELISA assay that compared the binding activity of an anti-KRAS G12D antibody 4F10 conjugate (KRAS^G12DiTAb (Compound 1)) and an anti-KRAS G12D 4F10 monoclonal antibody (anti-KRAS^G12D). Antibody and antibody conjugate concentration is shown on the x-axis and absorbance is on the y-axis.

FIG. 5A is a graph that shows the level of ERK 1/2 phosphorylation in U2OS KRAS wild type cells, in U2OS KRAS wild type cells stimulated with EGF, and in ASPC-1 cells with a KRAS G12D mutation after treatment with a control antibody conjugate (Control iTAbs) or treatment with anti-KRAS G12D 4F10 antibody conjugate (KRAS G12D iTAb (Compound 1)). Fully human IgGs against bacterial proteins were produced and modified with the same procedure as the anti-KRAS G12D antibody conjugates, then included as experimental control antibody conjugates.

FIG. 5B is a graph that shows the percent viability of the KRAS G12D cells after treatment with a control antibody conjugate (Control iTAbs) or treatment with an anti-KRAS G12D 4F10 antibody conjugate (KRAS G12D iTAb (Compound 1)). Fully human IgGs against bacterial proteins were produced and modified with the same procedure as the anti-KRAS G12D antibody conjugates, then included as experimental control antibody conjugates.

FIG. 6A is a graph showing that the anti-KRAS G12D 4F10 antibody conjugate (Compound 1) did not affect viability of U2OS cells. Control antibody conjugate (Control iTAb), anti-KRAS G12D 4F10 monoclonal antibody (KRAS^G12DmAb) and anti-KRAS G12D 4F10 antibody conjugate (KRAS^G12DiTAb (Compound 1)) were each tested. Percent viability is shown on the y-axis.

FIG. 6B is a graph that shows that the anti-KRAS G12D 4F10 antibody conjugate (Compound 1) had cytotoxic activity in ASPC-1 cells. Control antibody conjugate (Control iTAb), anti-KRAS G12D monoclonal antibody (KRAS^G12DmAb) and anti-KRAS G12D 4F10 antibody conjugate (KRAS^G12DiTAb (Compound 1)) were each tested. Percent viability is shown on the y-axis.

DETAILED DESCRIPTION
Definitions

An “antigen binding protein” is a protein comprising a portion that binds to an antigen and, optionally, a scaffold or framework portion that allows the antigen binding portion to adopt a confirmation that promotes binding of the antigen binding protein to the antigen. Examples of antigen binding proteins include antibodies, antibody fragments (i.e., an antigen binding portion of an antibody), antibody derivatives, and antibody analogs. The antigen binding protein can comprise, for example, an alternative protein scaffold or artificial scaffold with grafted CDRs or CDR derivatives. Such scaffolds include, but are not limited to, antibody-derived scaffolds comprising mutations introduced to, for example, stabilize the three-dimensional structure of the antigen binding protein as well as wholly synthetic scaffolds comprising, for example, a biocompatible polymer. See, for example, Korndorfer et al. (2003) Proteins: Structure, Function, and Bioinformatics, 53(1):121-129; Roque et al. (2004) Biotechnol. Prog. 20:639-654. In addition, peptide antibody mimetics (“PAMs”) can be used, as well as scaffolds based on antibody mimetics utilizing fibronectin components as a scaffold.

An “antigen binding domain,” “antigen binding region,” or “antigen binding site” is a portion of an antigen binding protein that contains amino acid residues (or other moieties) that interact with an antigen and contribute to the antigen binding protein's specificity and affinity for the antigen. For an antibody that specifically binds to its antigen, this will include at least one of its CDRs.

An “epitope” is the portion of a molecule that is bound by an antigen binding protein (e.g., by an antibody). Generally the variable regions, particularly the CDRs, of an antibody interact with the epitope.

The term “antibody” refers to an immunoglobulin (Ig) molecule comprised of four polypeptide chains, two heavy (H) chains and two light (L) chains, or any functional fragment, mutant, variant, or derivation thereof, which retains the essential epitope binding features of an Ig molecule.

Generally, the amino-terminal portion of each antibody chain includes a variable region, including three hypervariable complementarity determining regions (CDRs) that are primarily responsible for antigen recognition. The carboxy-terminal portion of each chain defines a constant region, e.g., responsible for effector function. Human light chains are classified as kappa or lambda light chains Heavy chains are classified as mu, delta, gamma, alpha, or epsilon, and define the antibody's isotype as IgM, IgD, IgG, IgA, and IgE, respectively. Within light and heavy chains, the variable and constant regions are joined by a “J” region of about 12 or more amino acids, with the heavy chain also including a “D” region of about 10 more amino acids. See generally, Fundamental Immunology Ch. 7 (Paul, W., ed., 2nd ed. Raven Press, N.Y. (1989)). The variable regions of each light/heavy chain pair form the antibody binding site such that an intact immunoglobulin has two binding sites. A single VH or VL domain may be sufficient to confer antigen-binding specificity.

The variable regions of antibody heavy and light chains (VH and VL, respectively) exhibit the same general structure of relatively conserved framework regions (FR) joined by three CDRs. From N-terminus to C-terminus, both light and heavy chains comprise the domains FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4. The assignment of amino acids to each domain is known in the art, including, for example, definitions as described in Kabat et al. in Sequences of Proteins of Immunological Interest, 5^thEd., US Dept. of Health and Human Services, PHS, NIH, NIH Publication no. 91-3242, 1991 (herein referred to as “Kabat numbering”). For example, the CDR regions of an antibody can be determined according to Kabat numbering.

The terms “intact antibody” or “full length antibody” refer to an antibody composed of two identical antibody light chains and two identical antibody heavy chains that each contain an Fc region.

The term “Fc polypeptide” includes native and mutein forms of polypeptides derived from the Fc region of an antibody. Truncated forms of such polypeptides containing the hinge region that promotes dimerization also are included. Fusion proteins comprising Fc moieties (and oligomers formed therefrom) offer the advantage of facile purification by affinity chromatography over Protein A or Protein G columns.

The terms “anti-KRAS antibody” and “an antibody that binds to KRAS” refer to an antibody that is capable of binding KRAS with sufficient affinity such that the antibody is useful as a diagnostic and/or therapeutic agent in targeting KRAS, including human KRAS.

The term “monospecific”, as used herein, refers to an antibody, or antigen binding fragment thereof, that displays an affinity for one particular epitope. In contrast, a bispecific antibody, or antigen-binding fragment thereof, displays affinity for two different epitopes. In one embodiment, the methods and compositions described herein are useful for intracellular delivery of a monospecific antibody, or antigen-binding fragment thereof. In one embodiment, the anti-KRAS antibody, or antigen-binding fragment thereof, of the invention is monospecific.

A “multi-specific antibody” is an antibody that recognizes more than one epitope on one or more antigens. A subclass of this type of antibody is a “bispecific antibody” which recognizes two distinct epitopes on the same or different antigens.

The terms “specific binding”, “specifically binds” or “specifically binding”, as used herein in the context of an antibody, refer to non-covalent or covalent preferential binding of an antibody to an antigen relative to other molecules or moieties (e.g., an antibody specifically binds to a particular antigen relative to other available antigens). In one embodiment, an antibody specifically binds to an antigen (e.g., KRAS) if it binds to the antigen with a dissociation constant K_Dof 10⁻⁵M or less (e.g., 10⁻⁶M or less, 10⁻⁷M or less, 10⁻⁸M or less, 10⁻⁹M or less, or 10⁻¹⁰M or less).

The term “human antibody”, as used herein, refers to an antibody, or an antigen binding fragment of an antibody, comprising heavy and lights chains derived from human immunoglobulin sequences. Human antibodies may be identified in a variety of ways, examples of which are described below, including through the immunization with an antigen of interest of a mouse that is genetically modified to express antibodies derived from human heavy and/or light chain-encoding genes. In one embodiment, a human antibody is made using recombinant methods such that the glycosylation pattern of the antibody is different than an antibody having the same sequence if it were to exist in nature.

The term “chimeric antibody” refers to an antibody that contains one or more regions derived from a particular source or species, and one or more regions derived from a different source or species.

A “humanized antibody” is an antibody or a variant, derivative, analog, or fragment thereof, which specifically binds to an antigen of interest and which comprises a framework (FR) region having substantially the amino acid sequence of a human antibody and a complementary determining region (CDR) having substantially the amino acid sequence of a non-human antibody. Generally, a humanized antibody is less likely to induce an immune response, and/or induces a less severe immune response, as compared to the non-human species antibody, e.g., a murine or chimeric antibody, when it is administered to a human subject. In one embodiment, certain amino acids in the framework and constant domains of the heavy and/or light chains of the non-human species antibody are mutated to produce the humanized antibody. Examples of how to make humanized antibodies may be found in U.S. Pat. Nos. 6,054,297, 5,886,152 and 5,877,293.

An “antibody fragment”, “antibody portion”, “antigen-binding fragment of an antibody”, or “antigen-binding portion of an antibody” refers to a molecule other than an intact antibody that comprises a portion of an intact antibody that binds the antigen to which the intact antibody binds. Examples of antibody fragments include, but are not limited to, Fv, Fab, Fab′, Fab′-SH, F(ab′)₂; Fd; and Fv fragments, as well as dAb; diabodies; linear antibodies; single-chain antibody molecules (e.g. scFv); polypeptides that contain at least a portion of an antibody that is sufficient to confer specific antigen binding to the polypeptide. Antigen binding portions of an antibody may be produced by recombinant DNA techniques or by enzymatic or chemical cleavage of intact antibodies. Antigen binding portions include, inter alia, Fab, Fab′, F(ab′)2, Fv, domain antibodies (dAbs), and complementarity determining region (CDR) fragments, chimeric antibodies, diabodies, triabodies, tetrabodies, and

In one embodiment, the antibody fragment is an scFv. A single-chain antibody (scFv) is an antibody in which a V_Land a V_Hregion are joined via a linker (e.g., a synthetic sequence of amino acid residues) to form a continuous protein chain (see e.g., Bird et al. (1988) Science 242:423-426; and Huston et al. (1988) Proc. Natl. Acad. Sci. USA 85:5879-5883)).

A Fab fragment is a monovalent fragment having the V_L, V_H, C_Land C_H1domains; a F(ab′)₂fragment is a bivalent fragment having two Fab fragments linked by a disulfide bridge at the hinge region; a Fd fragment has the V_Hand C_H1domains; an Fv fragment has the V_Land V_Hdomains of a single arm of an antibody; and a dAb fragment has a V_Hdomain, a V_Ldomain, or an antigen-binding fragment of a V_Hor V_Ldomain (U.S. Pat. Nos. 6,846,634; 6,696,245, US Patent Publication Nos. 2005/0202512; 2004/0202995; 2004/0038291; 2004/0009507; 2003/0039958, and Ward et al., Nature 341:544-546, 1989).

Diabodies are bivalent antibodies comprising two polypeptide chains, wherein each polypeptide chain comprises VH and VL domains joined by a linker that is too short to allow for pairing between two domains on the same chain, thus allowing each domain to pair with a complementary domain on another polypeptide chain (see, e.g., Holliger et al. (1993) Proc. Natl. Acad. Sci. USA 90:6444-48, and Poljak et al. (1994) Structure 2:1121-23). If the two polypeptide chains of a diabody are identical, then a diabody resulting from their pairing will have two identical antigen binding sites. Polypeptide chains having different sequences can be used to make a diabody with two different antigen binding sites. Similarly, tribodies and tetrabodies are antibodies comprising three and four polypeptide chains, respectively, and forming three and four antigen binding sites, respectively, which can be the same or different.

The “percent identity” or “percent homology” of two polynucleotide or two polypeptide sequences is determined by comparing the sequences using the GAP computer program (a part of the GCG Wisconsin Package, version 10.3 (Accelrys, San Diego, Calif.)) using its default parameters.

The terms “polynucleotide,” “oligonucleotide” and “nucleic acid” are used interchangeably throughout and include DNA molecules (e.g., cDNA or genomic DNA), RNA molecules (e.g., mRNA), analogs of the DNA or RNA generated using nucleotide analogs (e.g., peptide nucleic acids and non-naturally occurring nucleotide analogs), and hybrids thereof. The nucleic acid molecule can be single-stranded or double-stranded. In one embodiment, the nucleic acid molecules of the invention comprise a contiguous open reading frame encoding an antibody, or a fragment, derivative, mutein, or variant thereof.

Two single-stranded polynucleotides are “the complement” of each other if their sequences can be aligned in an anti-parallel orientation such that every nucleotide in one polynucleotide is opposite its complementary nucleotide in the other polynucleotide, without the introduction of gaps, and without unpaired nucleotides at the 5′ or the 3′ end of either sequence. A polynucleotide is “complementary” to another polynucleotide if the two polynucleotides can hybridize to one another under moderately stringent conditions. Thus, a polynucleotide can be complementary to another polynucleotide without being its complement.

A “vector” is a nucleic acid that can be used to introduce another nucleic acid linked to it into a cell. One type of vector is a “plasmid,” which refers to a linear or circular double stranded DNA molecule into which additional nucleic acid segments can be ligated. Another type of vector is a viral vector (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), wherein additional DNA segments can be introduced into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors comprising a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. An “expression vector” is a type of vector that can direct the expression of a chosen polynucleotide.

A nucleotide sequence is “operably linked” to a regulatory sequence if the regulatory sequence affects the expression (e.g., the level, timing, or location of expression) of the nucleotide sequence. A “regulatory sequence” is a nucleic acid that affects the expression (e.g., the level, timing, or location of expression) of a nucleic acid to which it is operably linked. The regulatory sequence can, for example, exert its effects directly on the regulated nucleic acid, or through the action of one or more other molecules (e.g., polypeptides that bind to the regulatory sequence and/or the nucleic acid). Examples of regulatory sequences include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Further examples of regulatory sequences are described in, for example, Goeddel (1990) Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. and Baron et al. (1995) Nucleic Acids Res. 23:3605-06.

A “host cell” is a cell that can be used to express a nucleic acid, e.g., a nucleic acid of the invention. A host cell can be a prokaryote, for example, E. coli, or it can be a eukaryote, for example, a single-celled eukaryote (e.g., a yeast or other fungus), a plant cell (e.g., a tobacco or tomato plant cell), an animal cell (e.g., a human cell, a monkey cell, a hamster cell, a rat cell, a mouse cell, or an insect cell) or a hybridoma. Examples of host cells include the COS-7 line of monkey kidney cells (ATCC CRL 1651) (see Gluzman et al. (1981) Cell 23:175), L cells, C127 cells, 3T3 cells (ATCC CCL 163), Chinese hamster ovary (CHO) cells or their derivatives such as Veggie CHO and related cell lines which grow in serum-free media (see Rasmussen et al. (1998) Cytotechnology 28:31) or CHO strain DX-B11, which is deficient in DHFR (see Urlaub et al. (1980) Proc. Natl. Acad. Sci. USA 77:4216-20), HeLa cells, BHK (ATCC CRL 10) cell lines, the CV1/EBNA cell line derived from the African green monkey kidney cell line CV1 (ATCC CCL 70) (see McMahan et al. (1991) EMBO J. 10:2821), human embryonic kidney cells such as 293,293 EBNA or MSR 293, human epidermal A431 cells, human Colo205 cells, other transformed primate cell lines, normal diploid cells, cell strains derived from in vitro culture of primary tissue, primary explants, HL-60, U937, HaK or Jurkat cells. In one embodiment, a host cell is a mammalian host cell, but is not a human host cell. Typically, a host cell is a cultured cell that can be transformed or transfected with a polypeptide-encoding nucleic acid, which can then be expressed in the host cell. The phrase “recombinant host cell” can be used to denote a host cell that has been transformed or transfected with a nucleic acid to be expressed. A host cell also can be a cell that comprises the nucleic acid but does not express it at a desired level unless a regulatory sequence is introduced into the host cell such that it becomes operably linked with the nucleic acid. It is understood that the term host cell refers not only to the particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to, e.g., mutation or environmental influence, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.

The term “recombinant antibody” refers to an antibody that is expressed from a cell or cell line transfected with an expression vector (or possibly more than one expression vector) comprising the coding sequence of the antibody, or a portion thereof (e.g., a DNA sequence encoding a heavy chain or a light chain). In one embodiment, said coding sequence is not naturally associated with the cell. In one embodiment, a recombinant antibody has a glycosylation pattern that is different than the glycosylation pattern of an antibody having the same sequence if it were to exist in nature. In one embodiment, a recombinant antibody is expressed in a mammalian host cell which is not a human host cell. Notably, individual mammalian host cells have unique glycosylation patterns.

The term “effective amount” as used herein, refers to that amount of an antibody, or an antigen binding portion thereof, that binds KRAS which is sufficient to effect treatment of a disease associated with KRAS signaling when administered to a subject. Therapeutically effective amounts of antibodies provided herein, when used alone or in combination, will vary depending upon the relative activity of the antibodies and combinations (e.g., in inhibiting cell growth) and depending upon the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, the manner of administration and the like, which can readily be determined by one of ordinary skill in the art.

The term “isolated” refers to a protein (e.g., an antibody) that is substantially free of other cellular material. In one embodiment, an isolated antibody is substantially free of other proteins from the same species. In one embodiment, an isolated antibody is expressed by a cell from a different species and is substantially free of other proteins from the different species. A protein may be rendered substantially free of naturally associated components (or components associated with the cellular expression system used to produce the antibody) by isolation, using protein purification techniques well known in the art. In one embodiment, the ant-KRAS antibodies, or antigen binding fragments, of the invention are isolated.

An “intracellular delivery compound” (also referred to herein as “conjugate” or “antibody conjugate”), as used herein, refers to a compound which is conjugated (covalently or non-covalently) to an antigen binding protein (e.g., an antibody or antibody fragment) which is capable of internalizing the antigen binding protein into a cell. Examples of intracellular delivery compounds (conjugated to an antibody) are provided in FIGS. 2A-2C.

The term “KRAS,” as used herein, refers to any native KRAS from any vertebrate source, including mammals such as primates (e.g., humans) and rodents (e.g., mice and rats), unless otherwise indicated. The term encompasses “full-length,” unprocessed KRAS as well as any form of KRAS that results from processing in the cell. The term also encompasses naturally occurring variants of KRAS, for example, splice variants or allelic variants. The amino acid sequence of an exemplary human KRAS isoform (variant (b)) is shown in SEQ ID NO. 305. This variant (b) is composed of five exons and lacks exon 4a which the longer transcript variant (a) includes. This predominant variant (b) has a cds that terminates in exon 4b and encodes isoform b.

(SEQ ID NO: 305)

1
mteyklvvvg aggvgksalt iqliqnhfvd eydptiedsy rkqvvidget clldildtag

61
qeeysamrdq ymrtgegflc vfainntksf edihhyreqi krvkdsedvp mvlvgnkcdl

121
psrtvdtkqa qdlarsygip fietsaktrq gvddafytlv reirkhkekm skdgkkkkkk

181
sktkcvim

In one embodiment, the antibody, or fragment, of the invention binds to human KRAS as set forth in SEQ ID NO: 305.

KRAS Antigen Binding Proteins

The invention provides anti-KRAS antigen binding proteins, e.g., antibodies and fragments thereof, as well as methods of using and making the same. In a preferred embodiment, the anti-KRAS antibodies, and antigen-binding fragments thereof, bind to human KRAS (hKRAS). The KRAS gene encodes a 21-kDa small protein that is activated transiently as a response to extracellular stimuli or signals such as growth factors, cytokines, and hormones via cell surface receptors.

The present invention pertains to KRAS binding proteins, particularly anti-KRAS antibodies, or antigen-binding portions thereof, that bind KRAS (e.g., human KRAS), and uses thereof. Various aspects of the invention relate to antibodies and antibody fragments, pharmaceutical compositions, nucleic acids, recombinant expression vectors, and host cells for making such antibodies and fragments. Methods of using the antibodies of the invention to detect human KRAS, to inhibit KRAS activity, either in vitro or in vivo, and to prevent or treat disorders such as cancer are also encompassed by the invention.

As described in Table 4 below, included in the invention are novel human antibody heavy and light chain variable regions and CDRs that are specific to human KRAS. In one embodiment, the invention provides an anti-KRAS antibody, or an antigen-binding fragment thereof, that comprises a heavy chain having a variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73. In one embodiment, the invention provides an anti-KRAS antibody, or an antigen-binding fragment thereof, that comprises a light chain having a variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74. In one embodiment, the invention provides an anti-KRAS antibody, or an antigen-binding fragment thereof, that comprises a light chain having a variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74; and a heavy chain having a variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73.

In one embodiment, the present disclosure provides a human antibody of an IgG class that binds to a human KRAS epitope with a binding affinity of at least 10⁻⁶M, where the antibody, or antigen-binding fragment, has a heavy chain variable domain sequence which is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, or identical, to an amino acid sequence selected from the group consisting of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73, and has a light chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, or identical to an amino acid sequence selected from the group consisting of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74.

In one embodiment, the invention includes an anti-KRAS antibody which is an IgG and comprises four polypeptide chains including two heavy chains each comprising a heavy chain variable domain and heavy chain constant regions C_H1, C_H2and C_H3, and two light chains each comprising a light chain variable domain and a light chain constant region (C_L). In certain embodiments, the antibody is an IgG1, IgG2, IgG3 or an IgG4. The heavy and light chain variable domain sequences may be selected from those described herein in SEQ ID Nos: 1-74.

Complementarity determining regions (CDRs) are known as hypervariable regions both in the light chain and the heavy chain variable domains. The more highly conserved portions of variable domains are called the framework (FR). Complementarity determining regions (CDRs) and framework regions (FR) of a given antibody may be identified using the numbering system described by Kabat et al. (1991) NIH Publication 91-3242, National Technical Information Service, Springfield, Va. An antigen binding protein may incorporate the CDR(s) as part of a larger polypeptide chain, may covalently link the CDR(s) to another polypeptide chain, or may incorporate the CDR(s) noncovalently. The CDRs permit the antigen binding protein to specifically bind to a particular antigen of interest.

In certain embodiments, the present invention provides an anti-KRAS antibody comprising the CDRs of the heavy and light chain variable domains described in Table 4 (SEQ ID Nos: 1 to 74). For example, the invention provides an anti-KRAS antibody, or antigen-binding fragment thereof, comprising a heavy chain variable region having the CDRs described in an amino acid sequence as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73. In one embodiment, the invention provides an anti-KRAS antibody, or antigen-binding fragment thereof, comprising a light chain variable region having the CDRs described in an amino acid sequence as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74. In one embodiment, the invention provides an anti-KRAS antibody, or antigen-binding fragment thereof, comprising a light chain variable region having the CDRs described in an amino acid sequence as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74; and a heavy chain variable region having the CDRs described in an amino acid sequence as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73.

In one embodiment, the invention includes an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, wherein the heavy chain variable domain is selected from the group consisting of a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 1 and comprising the heavy chain CDR set of SEQ ID Nos: 75, 76, and 77; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 3 and comprising the heavy chain CDR set of SEQ ID Nos: 81, 82 and 83; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 5 and comprising the heavy chain CDR set of SEQ ID Nos: 87, 88 and 89; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 7 and comprising the heavy chain CDR set of SEQ ID Nos: 93, 94 and 95; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 9 and comprising the heavy chain CDR set of SEQ ID Nos: 99, 100 and 101; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 11 and comprising the heavy chain CDR set of SEQ ID Nos: 105, 106 and 107; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 13 and comprising the heavy chain CDR set of SEQ ID Nos: 111, 112 and 113; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 15 and comprising the heavy chain CDR set of SEQ ID Nos: 117, 118 and 119; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 17 and comprising the heavy chain CDR set of SEQ ID Nos: 123, 124 and 125; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 19 and comprising the heavy chain CDR set of SEQ ID Nos: 129, 130 and 131; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 21 and comprising the heavy chain CDR set of SEQ ID Nos: 135, 136 and 137; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 23 and comprising the heavy chain CDR set of SEQ ID Nos: 141, 142 and 143; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 25 and comprising the heavy chain CDR set of SEQ ID Nos: 147, 148 and 149; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 27 and comprising the heavy chain CDR set of SEQ ID Nos: 153, 154 and 155; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 29 and comprising the heavy chain CDR set of SEQ ID Nos: 159, 160 and 161; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 31 and comprising the heavy chain CDR set of SEQ ID Nos: 165, 166 and 167; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 33 and comprising the heavy chain CDR set of SEQ ID Nos: 171, 172 and 173; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 35 and comprising the heavy chain CDR set of SEQ ID Nos: 177, 178 and 179; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 37 and comprising the heavy chain CDR set of SEQ ID Nos: 183, 184 and 185; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 39 and comprising the heavy chain CDR set of SEQ ID Nos: 189, 190 and 191; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 41 and comprising the heavy chain CDR set of SEQ ID Nos: 195, 196 and 197; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 43 and comprising the heavy chain CDR set of SEQ ID Nos: 201, 202 and 203; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 45 and comprising the heavy chain CDR set of SEQ ID Nos: 207, 208 and 209; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 47 and comprising the heavy chain CDR set of SEQ ID Nos: 213, 214 and 215; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 49 and comprising the heavy chain CDR set of SEQ ID Nos: 219, 220 and 221; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 51 and comprising the heavy chain CDR set of SEQ ID Nos: 225, 226 and 227; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 53 and comprising the heavy chain CDR set of SEQ ID Nos: 231, 232 and 233; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 55 and comprising the heavy chain CDR set of SEQ ID Nos: 237, 238 and 239; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 57 and comprising the heavy chain CDR set of SEQ ID Nos: 243, 244 and 245; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 59 and comprising the heavy chain CDR set of SEQ ID Nos: 249, 250 and 251; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 61 and comprising the heavy chain CDR set of SEQ ID Nos: 255, 256 and 257; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 63 and comprising the heavy chain CDR set of SEQ ID Nos: 261, 262 and 263; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 65 and comprising the heavy chain CDR set of SEQ ID Nos: 267, 268 and 269; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 67 and comprising the heavy chain CDR set of SEQ ID Nos: 273, 274 and 275; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 69 and comprising the heavy chain CDR set of SEQ ID Nos: 279, 280 and 281; a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 71 and comprising the heavy chain CDR set of SEQ ID Nos: 285, 286 and 287; and a heavy chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 73 and comprising the heavy chain CDR set of SEQ ID Nos: 291, 292 and 293; and comprises a light chain variable domain selected from the group consisting of a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 2 and comprising the light chain CDR set of SEQ ID Nos: 78, 79 and 80; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 4 and comprising the light chain CDR set of SEQ ID Nos: 84, 85 and 86; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 6 and comprising the light chain CDR set of SEQ ID Nos: 90, 91 and 92; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 8 and comprising the light chain CDR set of SEQ ID Nos: 96, 97 and 98; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 10 and comprising the light chain CDR set of SEQ ID Nos: 102, 103 and 104; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 12 and comprising the light chain CDR set of SEQ ID Nos: 108, 109 and 110; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 14 and comprising the light chain CDR set of SEQ ID Nos: 114, 115 and 116; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 16 and comprising the light chain CDR set of SEQ ID Nos: 120, 121 and 122; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 18 and comprising the light chain CDR set of SEQ ID Nos: 126, 127 and 128; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 20 and comprising the light chain CDR set of SEQ ID Nos: 132, 133 and 134; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 22 and comprising the light chain CDR set of SEQ ID Nos: 138, 139 and 140; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 24 and comprising the light chain CDR set of SEQ ID Nos: 144, 145 and 146; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 26 and comprising the light chain CDR set of SEQ ID Nos: 150, 151 and 152; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 28 and comprising the light chain CDR set of SEQ ID Nos: 156, 157 and 158; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 30 and comprising the light chain CDR set of SEQ ID Nos: 163, 163 and 164; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 32 and comprising the light chain CDR set of SEQ ID Nos: 168, 169 and 170; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 34 and comprising the light chain CDR set of SEQ ID Nos: 174, 175 and 176; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 36 and comprising the light chain CDR set of SEQ ID Nos: 180, 181 and 182; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 38 and comprising the light chain CDR set of SEQ ID Nos: 186, 187 and 188; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 40 and comprising the light chain CDR set of SEQ ID Nos: 192, 193 and 194; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 42 and comprising the light chain CDR set of SEQ ID Nos: 198, 199 and 200; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 44 and comprising the light chain CDR set of SEQ ID Nos: 204, 205 and 206; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 46 and comprising the light chain CDR set of SEQ ID Nos: 210, 211 and 212; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 48 and comprising the light chain CDR set of SEQ ID Nos: 216, 217 and 218; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 50 and comprising the light chain CDR set of SEQ ID Nos: 222, 223 and 224; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 52 and comprising the light chain CDR set of SEQ ID Nos: 228, 229 and 227; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 54 and comprising the light chain CDR set of SEQ ID Nos: 234, 235 and 236; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 56 and comprising the light chain CDR set of SEQ ID Nos: 240, 241 and 242; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 58 and comprising the light chain CDR set of SEQ ID Nos: 246, 247 and 248; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 60 and comprising the light chain CDR set of SEQ ID Nos: 252, 253 and 254; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 62 and comprising the light chain CDR set of SEQ ID Nos: 258, 259 and 260; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 64 and comprising the light chain CDR set of SEQ ID Nos: 264, 265 and 266; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 66 and comprising the light chain CDR set of SEQ ID Nos: 270, 271 and 272; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 68 and comprising the light chain CDR set of SEQ ID Nos: 276, 277 and 278; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 70 and comprising the light chain CDR set of SEQ ID Nos: 282, 283 and 284; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 72 and comprising the light chain CDR set of SEQ ID Nos: 288, 289 and 290; a light chain variable domain comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 74 and comprising the light chain CDR set of SEQ ID Nos: 294, 295 and 296.

In one embodiment, the present disclosure provides a fully human antibody of an IgG class that binds to a KRAS epitope with a binding affinity of 10⁻⁶M or less, that has a heavy chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, at least 99% identical, or 100% identical to an amino acid sequence selected from SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73; and that has a light chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, at least 99% identical, or 100% identical to an amino acid sequence selected from SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74.

In one embodiment, the invention provides an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain comprising a CDR3 domain as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73, and comprising a variable domain comprising an amino acid sequence that has at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% identical to a sequence as set forth in any one of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73. In one embodiment, the invention provides an anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a light chain comprising a CDR3 domain as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74, and having a light chain variable domain comprising an amino acid sequence that has at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% identical to a sequence as set forth in any one of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74. Thus, in certain embodiments, the CDR3 domain is held constant, while variability may be introduced into the remaining CDRs and/or framework regions of the heavy and/or light chains, while the antibody, or antigen binding fragment thereof, retains the ability to bind to KRAS and retains the functional characteristics, e.g., binding affinity, of the parent.

In one embodiment, the present invention features an isolated human anti-human KRAS (hKRAS) antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain comprising a heavy chain CDR set (CDR1, CDR2, and CDR3) selected from the group consisting of SEQ ID Nos. 75, 76 and 77; SEQ ID Nos. 81, 82 and 83; SEQ ID Nos. 87, 88 and 89; SEQ ID Nos. 93, 94 and 95; SEQ ID Nos. 99, 100 and 101; SEQ ID Nos. 105, 106 and 107; SEQ ID Nos. 111, 112 and 113; SEQ ID Nos. 117, 118 and 119; SEQ ID Nos. 123, 124 and 125; SEQ ID Nos. 129, 130 and 131; SEQ ID Nos. 135, 136 and 137; SEQ ID Nos. 141, 142 and 143; SEQ ID Nos. 147, 148 and 149; SEQ ID Nos. 153, 154 and 155; SEQ ID Nos. 159, 160, 161; SEQ ID Nos. 165, 166 and 167; SEQ ID Nos. 171, 172 and 173; SEQ ID Nos. 177, 178 and 179; SEQ ID Nos. 183, 184 and 185; SEQ ID Nos. 189, 190 and 191; SEQ ID Nos. 195, 196 and 197; SEQ ID Nos. 201, 202 and 203; SEQ ID Nos. 207, 208 and 209; SEQ ID Nos. 213, 214 and 215; SEQ ID Nos. 219, 220 and 221; SEQ ID Nos. 225, 226 and 227; SEQ ID Nos. 231, 232 and 233; SEQ ID Nos. 237, 238 and 239; SEQ ID Nos. 243, 244 and 245; SEQ ID Nos. 249, 250 and 251; SEQ ID Nos. 255, 256 and 257; SEQ ID Nos. 261, 262 and 263; SEQ ID Nos. 267, 268 and 269; SEQ ID Nos. 273, 274 and 275; SEQ ID Nos. 279, 280 and 281; SEQ ID Nos. 285, 286 and 287; and SEQ ID Nos. 291, 292 and 293; and a light chain variable domain comprising a light chain CDR set (CDR1, CDR2, and CDR3) selected from the group consisting of SEQ ID Nos. 78, 79 and 80; SEQ ID Nos. 84, 85 and 86; SEQ ID Nos. 90, 91 and 92; SEQ ID Nos. 96, 97 and 98; SEQ ID Nos. 102, 103 and 104; SEQ ID Nos. 108, 109 and 110; SEQ ID Nos. 114, 115 and 116; SEQ ID Nos. 120, 121 and 122; SEQ ID Nos. 126, 127 and 128; SEQ ID Nos. 132, 133 and 134; SEQ ID Nos. 138, 139 and 140; SEQ ID Nos. 144, 145 and 146; SEQ ID Nos. 150, 151 and 152; SEQ ID Nos. 156, 157 and 158; SEQ ID Nos. 162, 163 and 164; SEQ ID Nos. 168, 169 and 170; SEQ ID Nos. 174, 175 and 176; SEQ ID Nos. 180, 181 and 182; SEQ ID Nos. 186, 187 and 188; SEQ ID Nos. 192, 193 and 194; SEQ ID Nos. 198, 199 and 200; SEQ ID Nos. 204, 205 and 206; SEQ ID Nos. 210, 211 and 212; SEQ ID Nos. 216, 217 and 218; SEQ ID Nos. 222, 223 and 224; SEQ ID Nos. 228, 229 and 230; SEQ ID Nos. 234, 235 and 236; SEQ ID Nos. 240, 241 and 242; SEQ ID Nos. 246, 247 and 248; SEQ ID Nos. 252, 253 and 254; SEQ ID Nos. 258, 259 and 260; SEQ ID Nos. 264, 265 and 266; SEQ ID Nos. 270, 271 and 272; 276, 277 and 278; SEQ ID Nos. 282, 283 and 284; SEQ ID Nos. 288, 289 and 290; and SEQ ID Nos. 294, 295 and 296.

In one embodiment, the antibody of the invention comprises a heavy chain CDR set/light chain CDR set selected from the group consisting of the heavy chain variable domain CDR set of SEQ ID Nos: 75, 76 and 77 and the light chain variable domain CDR set of 78, 79 and 80; the heavy chain variable domain CDR set of SEQ ID Nos: 81, 82 and 83 and the light chain variable domain CDR set of 84, 85 and 86; the heavy chain variable domain CDR set of SEQ ID Nos: 87, 88 and 89 and the light chain variable domain CDR set of 90, 91 and 92; the heavy chain variable domain CDR set of SEQ ID Nos: 93, 94 and 95 and the light chain variable domain CDR set of 96, 97 and 98; the heavy chain variable domain CDR set of SEQ ID Nos: 99, 100 and 101 and the light chain variable domain CDR set of 102, 103 and 104; the heavy chain variable domain CDR set of SEQ ID Nos: 105, 106 and 107 and the light chain variable domain CDR set of 108, 109 and 110; the heavy chain variable domain CDR set of SEQ ID Nos: 111, 112 and 113 and the light chain variable domain CDR set of 114, 115 and 116; the heavy chain variable domain CDR set of SEQ ID Nos: 117, 118 and 119 and the light chain variable domain CDR set of 120, 121 and 122; the heavy chain variable domain CDR set of SEQ ID Nos: 123, 124 and 125 and the light chain variable domain CDR set of 126, 127 and 128; the heavy chain variable domain CDR set of SEQ ID Nos: 129, 130 and 131 and the light chain variable domain CDR set of 132, 133 and 134; the heavy chain variable domain CDR set of SEQ ID Nos: 135, 136 and 137 and the light chain variable domain CDR set of 138, 139 and 140; the heavy chain variable domain CDR set of SEQ ID Nos: 141, 142 and 143 and the light chain variable domain CDR set of 144, 145 and 146; the heavy chain variable domain CDR set of SEQ ID Nos: 147, 148 and 149 and the light chain variable domain CDR set of 150, 151 and 152; the heavy chain variable domain CDR set of SEQ ID Nos: 153, 154 and 155 and the light chain variable domain CDR set of 156, 157 and 158; the heavy chain variable domain CDR set of SEQ ID Nos: 159, 160 and 161 and the light chain variable domain CDR set of 162, 163 and 164; the heavy chain variable domain CDR set of SEQ ID Nos: 165, 166 and 167 and the light chain variable domain CDR set of 168, 169 and 170; the heavy chain variable domain CDR set of SEQ ID Nos: 171, 172 and 173 and the light chain variable domain CDR set of 174, 175 and 176; the heavy chain variable domain CDR set of SEQ ID Nos: 177, 178 and 179 and the light chain variable domain CDR set of 180, 181 and 182; the heavy chain variable domain CDR set of SEQ ID Nos: 183, 184 and 185 and the light chain variable domain CDR set of 186, 187 and 188; the heavy chain variable domain CDR set of SEQ ID Nos: 189, 190 and 191 and the light chain variable domain CDR set of 192, 193 and 194; the heavy chain variable domain CDR set of SEQ ID Nos: 195, 196 and 197 and the light chain variable domain CDR set of 198, 199 and 200; the heavy chain variable domain CDR set of SEQ ID Nos: 201, 202 and 203 and the light chain variable domain CDR set of 204, 205 and 206; the heavy chain variable domain CDR set of SEQ ID Nos: 207, 208 and 209 and the light chain variable domain CDR set of 210, 211 and 212; the heavy chain variable domain CDR set of SEQ ID Nos: 213, 1214 and 215 and the light chain variable domain CDR set of 216, 217 and 218; the heavy chain variable domain CDR set of SEQ ID Nos: 219, 220 and 221 and the light chain variable domain CDR set of 222, 223 and 224; the heavy chain variable domain CDR set of SEQ ID Nos: 225, 226 and 227 and the light chain variable domain CDR set of 228, 229 and 230; the heavy chain variable domain CDR set of SEQ ID Nos: 231, 232 and 233 and the light chain variable domain CDR set of 234, 235 and 236; the heavy chain variable domain CDR set of SEQ ID Nos: 237, 238 and 239 and the light chain variable domain CDR set of 240, 241 and 242; the heavy chain variable domain CDR set of SEQ ID Nos: 243, 244 and 245 and the light chain variable domain CDR set of 246, 247 and 248; the heavy chain variable domain CDR set of SEQ ID Nos: 249, 250 and 251 and the light chain variable domain CDR set of 252, 253 and 254; the heavy chain variable domain CDR set of SEQ ID Nos: 255, 256 and 257 and the light chain variable domain CDR set of 258, 259 and 260; the heavy chain variable domain CDR set of SEQ ID Nos: 261, 262 and 263 and the light chain variable domain CDR set of 1264, 265 and 266; the heavy chain variable domain CDR set of SEQ ID Nos: 267, 268 and 269 and the light chain variable domain CDR set of 270, 271 and 272; the heavy chain variable domain CDR set of SEQ ID Nos: 273, 274 and 275 and the light chain variable domain CDR set of 276, 277 and 278; the heavy chain variable domain CDR set of SEQ ID Nos: 279, 280 and 281 and the light chain variable domain CDR set of 282, 283 and 284; the heavy chain variable domain CDR set of SEQ ID Nos: 285, 286 and 287 and the light chain variable domain CDR set of 288, 289 and 290; and the heavy chain variable domain CDR set of SEQ ID Nos: 291, 292 and 293 and the light chain variable domain CDR set of 294, 295 and 296.

In one embodiment, the substitutions made within a heavy or light chain that is at least 95% identical (or at least 96% identical, or at least 97% identical, or at least 98% identical, or at least 99% identical) are conservative amino acid substitutions. A “conservative amino acid substitution” is one in which an amino acid residue is substituted by another amino acid residue having a side chain (R group) with similar chemical properties (e.g., charge or hydrophobicity). In general, a conservative amino acid substitution will not substantially change the functional properties of a protein. In cases where two or more amino acid sequences differ from each other by conservative substitutions, the percent sequence identity or degree of similarity may be adjusted upwards to correct for the conservative nature of the substitution. Means for making this adjustment are well-known to those of skill in the art. See, e.g., Pearson (1994) Methods Mol. Biol. 24: 307-331, herein incorporated by reference. Examples of groups of amino acids that have side chains with similar chemical properties include (1) aliphatic side chains: glycine, alanine, valine, leucine and isoleucine; (2) aliphatic-hydroxyl side chains: serine and threonine; (3) amide-containing side chains: asparagine and glutamine; (4) aromatic side chains: phenylalanine, tyrosine, and tryptophan; (5) basic side chains: lysine, arginine, and histidine; (6) acidic side chains: aspartate and glutamate, and (7) sulfur-containing side chains are cysteine and methionine.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having the antigen binding regions of any of the antibodies described in Table 4. The antibodies of the invention, including those described in Table 4, bind to human KRAS. In one aspect, the present invention is directed to an isolated anti-KRAS antibody, or an antigen-binding fragment thereof, comprising a heavy chain variable domain and a light chain variable domain selected from the group consisting of the heavy chain variable domain of SEQ ID NO: 1 and the light chain variable domain of SEQ ID NO: 2; the heavy chain variable domain of SEQ ID NO: 3 and the light chain variable domain of SEQ ID NO: 4; the heavy chain variable domain of SEQ ID NO: 5 and the light chain variable domain of SEQ ID NO: 6; the heavy chain variable domain of SEQ ID NO: 7 and the light chain variable domain of SEQ ID NO: 8; the heavy chain variable domain of SEQ ID NO: 9 and the light chain variable domain of SEQ ID NO: 10; the heavy chain variable domain of SEQ ID NO: 11 and the light chain variable domain of SEQ ID NO: 12; the heavy chain variable domain of SEQ ID NO: 13 and the light chain variable domain of SEQ ID NO: 14; the heavy chain variable domain of SEQ ID NO: 15 and the light chain variable domain of SEQ ID NO: 16; the heavy chain variable domain of SEQ ID NO: 17 and the light chain variable domain of SEQ ID NO: 18; the heavy chain variable domain of SEQ ID NO: 19 and the light chain variable domain of SEQ ID NO: 20; the heavy chain variable domain of SEQ ID NO: 21 and the light chain variable domain of SEQ ID NO: 22; the heavy chain variable domain of SEQ ID NO: 23 and the light chain variable domain of SEQ ID NO: 24; the heavy chain variable domain of SEQ ID NO: 25 and the light chain variable domain of SEQ ID NO: 26; the heavy chain variable domain of SEQ ID NO: 27 and the light chain variable domain of SEQ ID NO: 28; the heavy chain variable domain of SEQ ID NO: 29 and the light chain variable domain of SEQ ID NO: 30; the heavy chain variable domain of SEQ ID NO: 31 and the light chain variable domain of SEQ ID NO: 32; the heavy chain variable domain of SEQ ID NO: 33 and the light chain variable domain of SEQ ID NO: 34; the heavy chain variable domain of SEQ ID NO: 35 and the light chain variable domain of SEQ ID NO: 36; the heavy chain variable domain of SEQ ID NO: 37 and the light chain variable domain of SEQ ID NO: 38; the heavy chain variable domain of SEQ ID NO: 39 and the light chain variable domain of SEQ ID NO: 40; the heavy chain variable domain of SEQ ID NO: 41 and the light chain variable domain of SEQ ID NO: 42; the heavy chain variable domain of SEQ ID NO: 43 and the light chain variable domain of SEQ ID NO: 44; the heavy chain variable domain of SEQ ID NO: 45 and the light chain variable domain of SEQ ID NO: 46; the heavy chain variable domain of SEQ ID NO: 47 and the light chain variable domain of SEQ ID NO: 48; the heavy chain variable domain of SEQ ID NO: 49 and the light chain variable domain of SEQ ID NO: 50; the heavy chain variable domain of SEQ ID NO: 51 and the light chain variable domain of SEQ ID NO: 52; the heavy chain variable domain of SEQ ID NO: 53 and the light chain variable domain of SEQ ID NO: 54; the heavy chain variable domain of SEQ ID NO: 55 and the light chain variable domain of SEQ ID NO: 56; the heavy chain variable domain of SEQ ID NO: 57 and the light chain variable domain of SEQ ID NO: 58; the heavy chain variable domain of SEQ ID NO: 59 and the light chain variable domain of SEQ ID NO: 60; the heavy chain variable domain of SEQ ID NO: 61 and the light chain variable domain of SEQ ID NO: 62; the heavy chain variable domain of SEQ ID NO: 63 and the light chain variable domain of SEQ ID NO: 64; the heavy chain variable domain of SEQ ID NO: 65 and the light chain variable domain of SEQ ID NO: 66; the heavy chain variable domain of SEQ ID NO: 67 and the light chain variable domain of SEQ ID NO: 68; the heavy chain variable domain of SEQ ID NO: 69 and the light chain variable domain of SEQ ID NO: 70; the heavy chain variable domain of SEQ ID NO: 71 and the light chain variable domain of SEQ ID NO: 72; and the heavy chain variable domain of SEQ ID NO: 73 and the light chain variable domain of SEQ ID NO: 74.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1F4. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 1, and a light chain variable domain sequence as set forth in SEQ ID NO: 2. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 1, and a light chain variable domain comprising the CDRs of SEQ ID NO: 2. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 1, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 2. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 77, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 76, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 75; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 80, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 79 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 78. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1A7. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 3, and a light chain variable domain sequence as set forth in SEQ ID NO: 4. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 3, and a light chain variable domain comprising the CDRs of SEQ ID NO: 4. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 3, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 4. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 83, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 82, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 81; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 86, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 85 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 84. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-2B2. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 5, and a light chain variable domain sequence as set forth in SEQ ID NO: 6. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 5, and a light chain variable domain comprising the CDRs of SEQ ID NO: 6. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 5, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 6. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 89, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 88, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 87; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 92, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 91 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 90. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-2C2. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 7, and a light chain variable domain sequence as set forth in SEQ ID NO: 8. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 7, and a light chain variable domain comprising the CDRs of SEQ ID NO: 8. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 7, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 8 In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 95, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 94, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 93; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 98, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 97 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 96. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-2H8. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 9, and a light chain variable domain sequence as set forth in SEQ ID NO: 10. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 9, and a light chain variable domain comprising the CDRs of SEQ ID NO: 10. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 9, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 10. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 101, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 100, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 99; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 104, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 103 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 102. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-3E8. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 11, and a light chain variable domain sequence as set forth in SEQ ID NO: 12. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 11, and a light chain variable domain comprising the CDRs of SEQ ID NO: 12. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 11, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 12. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 107, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 106, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 105; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 110, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 109 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 108. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4D9. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 13, and a light chain variable domain sequence as set forth in SEQ ID NO: 14. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 13, and a light chain variable domain comprising the CDRs of SEQ ID NO: 14. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 13, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 14. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 1133, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 112, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 111; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 116, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 115 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 114. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4F10. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 15, and a light chain variable domain sequence as set forth in SEQ ID NO: 16. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 15, and a light chain variable domain comprising the CDRs of SEQ ID NO: 16. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 15, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 16. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 119, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 118, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 117; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 122, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 121 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 120. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5H6. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 17, and a light chain variable domain sequence as set forth in SEQ ID NO: 18. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 17, and a light chain variable domain comprising the CDRs of SEQ ID NO: 18. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 17, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 18. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 125, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 124, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 123; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 128, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 127 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 126. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1F12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 19, and a light chain variable domain sequence as set forth in SEQ ID NO: 20. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 19, and a light chain variable domain comprising the CDRs of SEQ ID NO: 20. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 19, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 20. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 131, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 130, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 129; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 134, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 133 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 132. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1H12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 21, and a light chain variable domain sequence as set forth in SEQ ID NO: 22. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 21, and a light chain variable domain comprising the CDRs of SEQ ID NO: 22. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 21, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 22. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 137, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 136, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 135; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 140, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 139 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 138. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1C3. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 23, and a light chain variable domain sequence as set forth in SEQ ID NO: 24. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 23, and a light chain variable domain comprising the CDRs of SEQ ID NO: 24. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 23, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 24. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 143, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 142, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 141; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 146, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 145 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 144. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1D3. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 25, and a light chain variable domain sequence as set forth in SEQ ID NO: 26. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 25, and a light chain variable domain comprising the CDRs of SEQ ID NO: 26. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 25, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 26. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 149, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 148, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 147; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 152, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 151 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 150. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1E6. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 27, and a light chain variable domain sequence as set forth in SEQ ID NO: 28. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 27, and a light chain variable domain comprising the CDRs of SEQ ID NO: 28. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 27, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 28. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 155, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 154, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 153; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 158, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 157 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 156. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1F6. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 29, and a light chain variable domain sequence as set forth in SEQ ID NO: 30. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 29, and a light chain variable domain comprising the CDRs of SEQ ID NO: 30. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 29, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 30. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 161, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 160, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 159; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 164, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 163 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 162. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1G6. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 31, and a light chain variable domain sequence as set forth in SEQ ID NO: 32. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 31, and a light chain variable domain comprising the CDRs of SEQ ID NO: 32. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 31, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 32. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 167, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 166, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 165; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 170, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 169 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 168. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-1E3. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 33, and a light chain variable domain sequence as set forth in SEQ ID NO: 34. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 33, and a light chain variable domain comprising the CDRs of SEQ ID NO: 34. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 33, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 34. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 173, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 172, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 171; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 176, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 175 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 174. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-3D11. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 35, and a light chain variable domain sequence as set forth in SEQ ID NO: 36. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 36, and a light chain variable domain comprising the CDRs of SEQ ID NO: 36. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 35, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 36. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 179, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 178, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 177; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 182, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 181 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 180. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4E10. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 37, and a light chain variable domain sequence as set forth in SEQ ID NO: 38. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 37, and a light chain variable domain comprising the CDRs of SEQ ID NO: 38. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 37, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 38. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 185, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 184, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 183; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 188, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 187 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 186. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4F10. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 39, and a light chain variable domain sequence as set forth in SEQ ID NO: 40. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 39, and a light chain variable domain comprising the CDRs of SEQ ID NO: 40. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 39, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 40. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 191, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 190, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 189; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 194, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 193 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 192. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4A12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 41, and a light chain variable domain sequence as set forth in SEQ ID NO: 42. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 41, and a light chain variable domain comprising the CDRs of SEQ ID NO: 42. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 41, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 42. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 197, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 196, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 195; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 200, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 199 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 198. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4D12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 43, and a light chain variable domain sequence as set forth in SEQ ID NO: 44. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 43, and a light chain variable domain comprising the CDRs of SEQ ID NO: 44. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 43, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 44. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 203, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 202, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 201; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 206, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 205 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 204. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-4E12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 45, and a light chain variable domain sequence as set forth in SEQ ID NO: 46. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 45, and a light chain variable domain comprising the CDRs of SEQ ID NO: 46. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 45, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 46. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 209, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 208, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 207; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 212, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 211 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 210. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5C4. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 47, and a light chain variable domain sequence as set forth in SEQ ID NO: 48. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 47, and a light chain variable domain comprising the CDRs of SEQ ID NO: 48. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 47, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 48. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 215, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 214, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 213; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 218, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 217 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 216. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5A4. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 49, and a light chain variable domain sequence as set forth in SEQ ID NO: 50. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 49, and a light chain variable domain comprising the CDRs of SEQ ID NO: 50. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 49, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 50. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 221, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 220, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 219; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 224, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 223 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 222. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5B7. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 51, and a light chain variable domain sequence as set forth in SEQ ID NO: 52. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 51, and a light chain variable domain comprising the CDRs of SEQ ID NO: 52. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 51, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 52. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 227, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 226, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 225; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 230, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 229 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 228. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5F8. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 53, and a light chain variable domain sequence as set forth in SEQ ID NO: 54. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 53, and a light chain variable domain comprising the CDRs of SEQ ID NO: 54. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 53, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 54. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 233, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 232, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 231; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 236, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 235 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 234. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5D3. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 55, and a light chain variable domain sequence as set forth in SEQ ID NO: 56. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 55, and a light chain variable domain comprising the CDRs of SEQ ID NO: 56. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 55, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 56. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 239, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 238, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 237; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 242, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 241 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 240. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5G5. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 57, and a light chain variable domain sequence as set forth in SEQ ID NO: 58. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 57, and a light chain variable domain comprising the CDRs of SEQ ID NO: 58. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 57, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 58. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 245, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 244, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 243; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 248, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 247 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 246. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5A10. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 59, and a light chain variable domain sequence as set forth in SEQ ID NO: 60. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 59, and a light chain variable domain comprising the CDRs of SEQ ID NO: 60. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 59, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 60. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 251, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 250, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 249; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 254, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 253 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 252. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5B12. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 61, and a light chain variable domain sequence as set forth in SEQ ID NO: 62. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 61, and a light chain variable domain comprising the CDRs of SEQ ID NO: 62. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 61, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 62. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 257, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 256, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 255; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 260, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 259 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 258. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5C5. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 63, and a light chain variable domain sequence as set forth in SEQ ID NO: 64. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 63, and a light chain variable domain comprising the CDRs of SEQ ID NO: 64. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 63, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 64. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 263, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 262, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 261; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 266, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 265 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 264. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5F6. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 65, and a light chain variable domain sequence as set forth in SEQ ID NO: 66. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 65, and a light chain variable domain comprising the CDRs of SEQ ID NO: 66. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 65, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 66. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 269, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 268, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 267; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 272, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 271 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 270. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5H4. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 67, and a light chain variable domain sequence as set forth in SEQ ID NO: 68. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 67, and a light chain variable domain comprising the CDRs of SEQ ID NO: 68. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 67, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 68. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 275, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 274, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 273; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 278, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 277 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 277. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5H1. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 69, and a light chain variable domain sequence as set forth in SEQ ID NO: 70. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 69, and a light chain variable domain comprising the CDRs of SEQ ID NO: 70. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 69, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 70. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 281, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 280, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 279; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 284, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 283 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 282. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5E2. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 71, and a light chain variable domain sequence as set forth in SEQ ID NO: 72. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 71, and a light chain variable domain comprising the CDRs of SEQ ID NO: 72. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 71, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 72. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 287, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 286, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 285; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 290, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 289 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 288. The antibody may be an IgG1 or an IgG4 isotype.

In one embodiment, the present invention is directed to an antibody, or an antigen binding fragment thereof, having antigen binding regions of antibody K3-5F2. In one embodiment, the invention provides an antibody, or antigen-binding fragment thereof, comprising a heavy chain variable domain sequence as set forth in SEQ ID NO: 73, and a light chain variable domain sequence as set forth in SEQ ID NO: 74. In one embodiment, the invention is directed to an antibody having a heavy chain variable domain comprising the CDRs of SEQ ID NO: 73, and a light chain variable domain comprising the CDRs of SEQ ID NO: 74. In one embodiment, the invention features an isolated human antibody, or antigen-binding fragment thereof, that comprises a heavy chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 73, and comprises a light chain variable region having an amino acid sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical to the sequence set forth in SEQ ID NO: 74. In one embodiment, the invention features an anti-KRAS antibody, or an antigen-binding portion thereof, comprising a heavy chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 293, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 292, and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 291; and comprising a light chain variable region comprising a CDR3 domain comprising the amino acid as set forth in SEQ ID NO: 296, a CDR2 domain comprising the amino acid sequence as set forth in SEQ ID NO: 295 and a CDR1 domain comprising the amino acid sequence as set forth in SEQ ID NO: 294. The antibody may be an IgG1 or an IgG4 isotype.

Antigen-binding fragments of antigen binding proteins of the invention may be produced by conventional techniques. Examples of such fragments include, but are not limited to, Fab and F(ab′)2 fragments.

In certain embodiments, the present disclosure provides a Fab fully human antibody fragment, having a variable domain region from a heavy chain and a variable domain region from a light chain, wherein the heavy chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, to the amino acid sequences selected from the group consisting of SEQ ID NO. 1, SEQ ID NO. 3, SEQ ID NO. 5, SEQ ID NO. 7, SEQ ID NO. 9, SEQ ID NO. 11, SEQ ID NO. 13, SEQ ID NO. 15, SEQ ID NO. 17, SEQ ID NO. 19, SEQ ID NO. 21, SEQ ID NO. 23, SEQ ID NO. 25, SEQ ID NO. 27, SEQ ID NO. 29, SEQ ID NO. 31, SEQ ID NO. 33, SEQ ID NO. 35, SEQ ID NO. 37, SEQ ID NO. 39, SEQ ID NO. 41, SEQ ID NO. 43, SEQ ID NO. 45, SEQ ID NO. 47, SEQ ID NO. 49, SEQ ID NO. 51, SEQ ID NO. 53, SEQ ID NO. 55, SEQ ID NO. 57, SEQ ID NO. 59, SEQ ID NO. 61, SEQ ID NO. 63, SEQ ID NO. 65, SEQ ID NO. 67, SEQ ID NO. 69, SEQ ID NO. 71 and SEQ ID NO. 73, and that has a light chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, to the amino acid sequence selected from the group consisting of SEQ ID NO. 2, SEQ ID NO. 4, SEQ ID NO. 6, SEQ ID NO. 8, SEQ ID NO. 10, SEQ ID NO. 12, SEQ ID NO. 14, SEQ ID NO. 16, SEQ ID NO. 18, SEQ ID NO. 20, SEQ ID NO. 22, SEQ ID NO. 24, SEQ ID NO. 26, SEQ ID NO. 28, SEQ ID NO. 30, SEQ ID NO. 32, SEQ ID NO. 34, SEQ ID NO. 36, SEQ ID NO. 38, SEQ ID NO. 40, SEQ ID NO. 42, SEQ ID NO. 44, SEQ ID NO. 46, SEQ ID NO. 48, SEQ ID NO. 50, SEQ ID NO. 52, SEQ ID NO. 54, SEQ ID NO. 56, SEQ ID NO. 58, SEQ ID NO. 60, SEQ ID NO. 62, SEQ ID NO. 64, SEQ ID NO. 66, SEQ ID NO. 68, SEQ ID NO. 70, SEQ ID NO. 72 and SEQ ID NO. 74.

Preferably, the fully human antibody Fab fragment has both a heavy chain variable domain region and a light chain variable domain region wherein the antibody has a heavy chain/light chain variable domain sequence selected from SEQ ID NO. 1/SEQ ID NO. 2, SEQ ID NO. 3/SEQ ID NO. 4, SEQ ID NO. 5/SEQ ID NO. 6, SEQ ID NO. 7/SEQ ID NO. 8, SEQ ID NO. 9/SEQ ID NO. 10, SEQ ID NO. 11/SEQ ID NO. 12, SEQ ID NO. 13/SEQ ID NO. 14, SEQ ID NO. 15/SEQ ID NO. 16, SEQ ID NO. 17/SEQ ID NO. 18, SEQ ID NO. 19/SEQ ID NO. 20, SEQ ID NO. 21/SEQ ID NO. 22, SEQ ID NO. 23/SEQ ID NO. 24, SEQ ID NO. 25/SEQ ID NO. 26, SEQ ID NO. 27/SEQ ID NO. 28, SEQ ID NO. 29/SEQ ID NO. 30, SEQ ID NO. 31/SEQ ID NO. 32, SEQ ID NO. 33/SEQ ID NO. 34, SEQ ID NO. 35/SEQ ID NO. 36, SEQ ID NO. 37/SEQ ID NO. 38, SEQ ID NO. 39/SEQ ID NO. 40, SEQ ID NO. 41/SEQ ID NO. 42, SEQ ID NO. 43/SEQ ID NO. 44, SEQ ID NO. 45/SEQ ID NO. 46, SEQ ID NO. 47/SEQ ID NO. 48, SEQ ID NO. 49/SEQ ID NO. 50, SEQ ID NO. 151/SEQ ID NO. 52, SEQ ID NO. 53/SEQ ID NO. 54, SEQ ID NO. 55/SEQ ID NO. 56, SEQ ID NO. 57/SEQ ID NO. 58, SEQ ID NO. 59/SEQ ID NO. 60, SEQ ID NO. 61/SEQ ID NO. 62, SEQ ID NO. 63/SEQ ID NO. 64, SEQ ID NO. 65/SEQ ID NO. 66, SEQ ID NO. 67/SEQ ID NO. 68, SEQ ID NO. 69/SEQ ID NO. 70, SEQ ID NO. 71/SEQ ID NO. 72 and SEQ ID NO. 73/SEQ ID NO. 74.

Single chain antibodies may be formed by linking heavy and light chain variable domain (Fv region) fragments via an amino acid bridge (short peptide linker), resulting in a single polypeptide chain Such single-chain Fvs (scFvs) have been prepared by fusing DNA encoding a peptide linker between DNAs encoding the two variable domain polypeptides (V_Land V_H). The resulting polypeptides can fold back on themselves to form antigen-binding monomers, or they can form multimers (e.g., dimers, trimers, or tetramers), depending on the length of a flexible linker between the two variable domains (Kortt et al. (1997) Prot. Eng. 10:423; Kortt et al. (2001) Biomol. Eng. 18:95-108). By combining different V_Land V_H-comprising polypeptides, one can form multimeric scFvs that bind to different epitopes (Kriangkum et al. (2001) Biomol. Eng. 18:31-40). Techniques developed for the production of single chain antibodies include those described in U.S. Pat. No. 4,946,778; Bird (1988) Science 242:423; Huston et al. (1988) Proc. Natl. Acad. Sci. USA 85:5879; Ward et al. (1989) Nature 334:544, de Graaf et al. (2002) Methods Mol. Biol. 178:379-87.

In one embodiment, the present disclosure provides an scFv having a variable domain region from a heavy chain and a variable domain region from a light chain and a peptide linker connection the heavy chain and light chain variable domain regions, wherein the heavy chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, to the amino acid sequences selected from SEQ ID NO: 1 or SEQ ID NO. 3, and that has a light chain variable domain sequence that is at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, or at least 99% identical, to the amino acid sequence selected from SEQ ID NO:2 or SEQ ID NO:4. In one embodiment, the scFv has both a heavy chain variable domain region and a light chain variable domain region, wherein the scFv has a heavy chain/light chain variable domain sequence selected from SEQ ID NO. 1/SEQ ID NO. 2, SEQ ID NO. 3/SEQ ID NO. 4, SEQ ID NO. 5/SEQ ID NO. 6, SEQ ID NO. 7/SEQ ID NO. 8, SEQ ID NO. 9/SEQ ID NO. 10, SEQ ID NO. 11/SEQ ID NO. 12, SEQ ID NO. 13/SEQ ID NO. 14, SEQ ID NO. 15/SEQ ID NO. 16, SEQ ID NO. 17/SEQ ID NO. 18, SEQ ID NO. 19/SEQ ID NO. 20, SEQ ID NO. 21/SEQ ID NO. 22, SEQ ID NO. 23/SEQ ID NO. 24, SEQ ID NO. 25/SEQ ID NO. 26, SEQ ID NO. 27/SEQ ID NO. 28, SEQ ID NO. 29/SEQ ID NO. 30, SEQ ID NO. 31/SEQ ID NO. 32, SEQ ID NO. 33/SEQ ID NO. 34, SEQ ID NO. 35/SEQ ID NO. 36, SEQ ID NO. 37/SEQ ID NO. 38, SEQ ID NO. 39/SEQ ID NO. 40, SEQ ID NO. 41/SEQ ID NO. 42, SEQ ID NO. 43/SEQ ID NO. 44, SEQ ID NO. 45/SEQ ID NO. 46, SEQ ID NO. 47/SEQ ID NO. 48, SEQ ID NO. 49/SEQ ID NO. 50, SEQ ID NO. 151/SEQ ID NO. 52, SEQ ID NO. 53/SEQ ID NO. 54, SEQ ID NO. 55/SEQ ID NO. 56, SEQ ID NO. 57/SEQ ID NO. 58, SEQ ID NO. 59/SEQ ID NO. 60, SEQ ID NO. 61/SEQ ID NO. 62, SEQ ID NO. 63/SEQ ID NO. 64, SEQ ID NO. 65/SEQ ID NO. 66, SEQ ID NO. 67/SEQ ID NO. 68, SEQ ID NO. 69/SEQ ID NO. 70, SEQ ID NO. 71/SEQ ID NO. 72 and SEQ ID NO. 73/SEQ ID NO. 74.

In one embodiment, the antibody of the invention is a human IgG1 antibody. In one embodiment, the antibody of the invention is a human IgG4 antibody.

Techniques are known for deriving an antibody of a different subclass or isotype from an antibody of interest, i.e., subclass switching. Thus, IgG antibodies may be derived from an IgM antibody, for example, and vice versa. Such techniques allow the preparation of new antibodies that possess the antigen-binding properties of a given antibody (the parent antibody), but also exhibit biological properties associated with an antibody isotype or subclass different from that of the parent antibody. Recombinant DNA techniques may be employed. Cloned DNA encoding particular antibody polypeptides may be employed in such procedures, e.g., DNA encoding the constant domain of an antibody of the desired isotype (Lantto et al. (2002) Methods Mol. Biol. 178:303-16). Moreover, if an IgG4 is desired, it may also be desired to introduce a point mutation (CPSCP→CPPCP) (SEQ ID Nos. 143 and 144, respectively) in the hinge region (Bloom et al. (1997) Protein Science 6:407) to alleviate a tendency to form intra-H chain disulfide bonds that can lead to heterogeneity in the IgG4 antibodies.

The present disclosure provides a number of antibodies structurally characterized by the amino acid sequences of their variable domain regions. However, the amino acid sequences can undergo some changes while retaining their high degree of binding to their specific targets. More specifically, many amino acids in the variable domain region can be changed with conservative substitutions and it is predictable that the binding characteristics of the resulting antibody will not differ from the binding characteristics of the wild type antibody sequence. There are many amino acids in an antibody variable domain that do not directly interact with the antigen or impact antigen binding and are not critical for determining antibody structure. For example, a predicted nonessential amino acid residue in any of the disclosed antibodies is preferably replaced with another amino acid residue from the same class. Methods of identifying amino acid conservative substitutions which do not eliminate antigen binding are well-known in the art (see, e.g., Brummell et al. (1993) Biochem. 32: 1180-1187; Kobayashi et al. (1997) Protein Eng. 12(10):879-884; and Burks et al. (1997) Proc. Natl. Acad. Sci. USA 94:412-417). Near et al. (1993) Mol. Immunol. 30:369-377 explains how to impact or not impact binding through site-directed mutagenesis. Near et al. only mutated residues that they thought had a high probability of changing antigen binding. Most had a modest or negative effect on binding affinity (Near et al., Table 3) and binding to different forms of digoxin (Near et al., Table 2).

Thus, the invention also includes, in certain embodiments, an antibody or a fragment thereof comprising light and/or heavy chain variable sequences having at least 95% identity to those sequences disclosed herein, wherein the antibody or fragment retains the characteristics of the parent antibody comprising the light and/or heavy chain variable sequences.

In certain embodiments, an antibody, or antigen-binding fragment thereof, provided herein has a dissociation constant (K_D) of 1×10⁻⁶M or less; 5×10⁻⁷M or less; 1×10⁻⁷M or less; 5×10⁻⁸M or less; 1×10⁻⁸M or less; 5×10⁻⁹M or less; or 1×10⁻⁹M or less. In one embodiment, the antibody, or antigen-binding fragment thereof, of the invention as a K_Dfrom 1×10⁻⁷M to 1×10⁻¹⁰M. In one embodiment, the antibody, or antigen-binding fragment thereof, of the invention as a K_Dfrom 1×10⁻⁸M to 1×10⁻¹⁰M.

Those of ordinary skill in the art will appreciate standard methods known for determining the K_Dof an antibody, or fragment thereof. For example, in one embodiment, K_Dis measured by a radiolabeled antigen binding assay (RIA). In one embodiment, an RIA is performed with the Fab version of an antibody of interest and its antigen. For example, solution binding affinity of Fabs for antigen is measured by equilibrating Fab with a minimal concentration of (¹²⁵I)-labeled antigen in the presence of a titration series of unlabeled antigen, then capturing bound antigen with an anti-Fab antibody-coated plate (see, e.g., Chen et al. (1999) J. Mol. Biol. 293:865-881).

According to another embodiment, K_Dis measured using a BIACORE surface plasmon resonance assay. The term “surface plasmon resonance”, as used herein, refers to an optical phenomenon that allows for the analysis of real-time interactions by detection of alterations in protein concentrations within a biosensor matrix, for example using the BIACORE system (Biacore Life Sciences division of GE Healthcare, Piscataway, N.J.).

In particular embodiments, antigen binding proteins of the present invention have a binding affinity (K_a) for KRAS of at least 10⁶M⁻¹. In other embodiments, the antigen binding proteins exhibit a K_aof at least 10⁷M⁻¹, at least 10⁸M⁻¹, at least 10⁹M⁻¹, or at least 10¹⁰M⁻¹. In another embodiment, the antigen binding protein exhibits a K_asubstantially the same as that of an antibody described herein in the Examples.

In another embodiment, the present disclosure provides an antigen binding protein that has a low dissociation rate from KRAS. In one embodiment, the antigen binding protein has a K_offof 1×10⁻⁴to sec⁻¹or lower. In another embodiment, the K_offis 5×10⁻⁵to sec⁻¹or lower. In another embodiment, the K_offis substantially the same as an antibody described herein. In another embodiment, the antigen binding protein binds to KRAS with substantially the same K_offas an antibody described herein.

In another aspect, the present disclosure provides an antigen binding protein that inhibits an activity of KRAS. In one embodiment, the antigen binding protein has an IC₅₀of 1000 nM or lower. In another embodiment, the IC₅₀is 100 nM or lower; in another embodiment, the IC₅₀is 10 nM or lower. In another embodiment, the IC₅₀is substantially the same as that of an antibody described herein in the Examples. In another embodiment, the antigen binding protein inhibits an activity of KRAS with substantially the same IC₅₀as an antibody described herein.

The present disclosure further provides multi-specific antigen binding proteins, for example, bispecific antigen binding protein, e.g., antigen binding protein that bind to two different epitopes of KRAS, or to an epitope of KRAS and an epitope of another molecule, via two different antigen binding sites or regions. Moreover, bispecific antigen binding protein as disclosed herein can comprise a KRAS binding site from one of the herein-described antibodies and a second KRAS binding region from another of the herein-described antibodies, including those described herein by reference to other publications. Alternatively, a bispecific antigen binding protein may comprise an antigen binding site from one of the herein described antibodies and a second antigen binding site from another KRAS antibody that is known in the art, or from an antibody that is prepared by known methods or the methods described herein.

Numerous methods of preparing bispecific antibodies are known in the art. Such methods include the use of hybrid-hybridomas as described by Milstein et al. (1983) Nature 305:537, and chemical coupling of antibody fragments (Brennan et al. (1985) Science 229:81; Glennie et al. (1987) J. Immunol. 139:2367; U.S. Pat. No. 6,010,902). Moreover, bispecific antibodies can be produced via recombinant means, for example by using leucine zipper moieties (i.e., from the Fos and Jun proteins, which preferentially form heterodimers; Kostelny et al. (1992) J. Immunol. 148:1547) or other lock and key interactive domain structures as described in U.S. Pat. No. 5,582,996. Additional useful techniques include those described in U.S. Pat. Nos. 5,959,083 and 5,807,706.

In another aspect, the antigen binding protein comprises a derivative of an antibody. The derivatized antibody can comprise any molecule or substance that imparts a desired property to the antibody, such as increased half-life in a particular use. The derivatized antibody can comprise, for example, a detectable (or labeling) moiety (e.g., a radioactive, colorimetric, antigenic or enzymatic molecule, a detectable bead (such as a magnetic or electrodense (e.g., gold) bead), or a molecule that binds to another molecule (e.g., biotin or streptavidin), a therapeutic or diagnostic moiety (e.g., a radioactive, cytotoxic, or pharmaceutically active moiety), or a molecule that increases the suitability of the antibody for a particular use (e.g., administration to a subject, such as a human subject, or other in vivo or in vitro uses). Examples of molecules that can be used to derivatize an antibody include albumin (e.g., human serum albumin) and polyethylene glycol (PEG). Albumin-linked and PEGylated derivatives of antibodies can be prepared using techniques well known in the art. In one embodiment, the antibody is conjugated or otherwise linked to transthyretin (TTR) or a TTR variant. The TTR or TTR variant can be chemically modified with, for example, a chemical selected from the group consisting of dextran, poly(n-vinyl pyurrolidone), polyethylene glycols, propropylene glycol homopolymers, polypropylene oxide/ethylene oxide co-polymers, polyoxyethylated polyols and polyvinyl alcohols.

In certain embodiments, the anti-KRAS antibody, or an antigen-binding fragment thereof is conjugated to an intracellular delivery compound. In one embodiment, the invention provides the compound of FIG. 2A. In one embodiment, the invention provides the compound of FIG. 2B. In one embodiment, the invention provides the compound of FIG. 2C. FIG. 2A is a drawing of an exemplary antibody conjugate of the present invention, comprising Formula (I), or a pharmaceutically acceptable salt thereof, wherein each of X, q, Ba, R1, r, t, L, and A_Tare as defined and described in U.S. Provisional Appln. No. 62/327,130, filed on Apr. 25, 2016, U.S. Provisional Appln. No. 62/327,132, filed on Apr. 25, 2016, U.S. Provisional Appln. No. 62/327,136, filed on Apr. 25, 2016, U.S. Provisional Appln. No. 62/327,137, filed on Apr. 25, 2016; and U.S. Publication No. 2017/0107289, filed on Oct. 20, 2016. FIG. 2B is a drawing of an embodiment of FIG. 2A, showing an exemplary antibody conjugate of the present invention, where the antibody (A_T) is an anti-KRAS antibody and the conjugate is labeled with fluorescein. FIG. 2C is a drawing of an embodiment of FIG. 2A, showing an exemplary antibody conjugate of the present invention, where the antibody (A_T) is an anti-KRAS antibody, and which is tested in Examples 1-9. In further exemplary embodiments, the antibody (A_T) is anti-KRAS G12D 4F10 antibody. This conjugate is termed Compound 1.

Oligomers that contain one or more antigen binding proteins may be employed as KRAS antagonists. Oligomers may be in the form of covalently-linked or non-covalently-linked dimers, trimers, or higher oligomers. Oligomers comprising two or more antigen binding protein are contemplated for use, with one example being a homodimer. Other oligomers include heterodimers, homotrimers, heterotrimers, homotetramers, heterotetramers, etc.

One embodiment is directed to oligomers comprising multiple antigen binding proteins joined via covalent or non-covalent interactions between peptide moieties fused to the antigen binding proteins. Such peptides may be peptide linkers (spacers), or peptides that have the property of promoting oligomerization. Leucine zippers and certain polypeptides derived from antibodies are among the peptides that can promote oligomerization of antigen binding proteins attached thereto, as described in more detail below.

In particular embodiments, the oligomers comprise from two to four antigen binding proteins. The antigen binding proteins of the oligomer may be in any form, such as any of the forms described above, e.g., variants or fragments. Preferably, the oligomers comprise antigen binding proteins that have KRAS binding activity.

Another method for preparing oligomeric antigen binding proteins involves use of a leucine zipper. Leucine zipper domains are peptides that promote oligomerization of the proteins in which they are found. Leucine zippers were originally identified in several DNA-binding proteins (Landschulz et al. (1988) Science 240:1759), and have since been found in a variety of different proteins. Among the known leucine zippers are naturally occurring peptides and derivatives thereof that dimerize or trimerize. Examples of leucine zipper domains suitable for producing soluble oligomeric proteins are described in WO 94/10308, and the leucine zipper derived from lung surfactant protein D (SPD) described in Hoppe et al. (1994) FEBS Letters 344:191. The use of a modified leucine zipper that allows for stable trimerization of a heterologous protein fused thereto is described in Fanslow et al. (1994) Semin. Immunol. 6:267-78. In one approach, recombinant fusion proteins comprising an anti-KRAS antibody fragment or derivative fused to a leucine zipper peptide are expressed in suitable host cells, and the soluble oligomeric anti-KRAS antibody fragments or derivatives that form are recovered from the culture supernatant.

Antigen binding proteins directed against KRAS can be used, for example, in assays to detect the presence of KRAS polypeptides, either in vitro or in vivo. The antigen binding proteins also may be employed in purifying KRAS proteins by immunoaffinity chromatography. Blocking antigen binding proteins can be used in the methods disclosed herein. Such antigen binding proteins that function as KRAS antagonists may be employed in treating any KRAS-induced condition, including but not limited to various cancers.

Antigen binding proteins may be employed in an in vitro procedure, or administered in vivo to inhibit KRAS-induced biological activity. Disorders that would benefit (directly or indirectly) from activation of KRAS, examples of which are provided herein, thus may be treated. In one embodiment, the present invention provides a therapeutic method comprising in vivo administration of a KRAS blocking antigen binding protein to a mammal in need thereof in an amount effective for reducing a KRAS-induced biological activity.

In certain embodiments of the invention, antigen binding proteins include fully human monoclonal antibodies that inhibit a biological activity of KRAS.

Antigen binding proteins, including antibodies and antibody fragments described herein, may be prepared by any of a number of conventional techniques. For example, they may be purified from cells that naturally express them (e.g., an antibody can be purified from a hybridoma that produces it), or produced in recombinant expression systems, using any technique known in the art. See, for example, Monoclonal Antibodies, Hybridomas: A New Dimension in Biological Analyses, Kennet et al. (eds.), Plenum Press, New York (1980); and Antibodies: A Laboratory Manual, Harlow and Land (eds.), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1988).

Any expression system known in the art can be used to make the recombinant polypeptides, including antibodies and antibody fragments described herein, of the invention. In general, host cells are transformed with a recombinant expression vector that comprises DNA encoding a desired polypeptide. Among the host cells that may be employed are prokaryotes, yeast or higher eukaryotic cells. Prokaryotes include gram negative or gram positive organisms, for example E. coli or bacilli. Higher eukaryotic cells include insect cells and established cell lines of mammalian origin. Examples of suitable mammalian host cell lines include the COS-7 line of monkey kidney cells (ATCC CRL 1651) (Gluzman et al. (1981) Cell 23:175), L cells, 293 cells, C127 cells, 3T3 cells (ATCC CCL 163), Chinese hamster ovary (CHO) cells, HeLa cells, BHK (ATCC CRL 10) cell lines, and the CV1/EBNA cell line derived from the African green monkey kidney cell line CV1 (ATCC CCL 70) as described by McMahan et al. (1991) EMBO J. 10: 2821. Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts are described by Pouwels et al. (Cloning Vectors: A Laboratory Manual, Elsevier, N.Y., 1985).

The transformed cells can be cultured under conditions that promote expression of the polypeptide, and the polypeptide recovered by conventional protein purification procedures. One such purification procedure includes the use of affinity chromatography, e.g., over a matrix having all or a portion (e.g., the extracellular domain) of KRAS bound thereto. Polypeptides contemplated for use herein include substantially homogeneous recombinant mammalian anti-KRAS antibody polypeptides substantially free of contaminating endogenous materials.

Antigen binding proteins may be prepared, and screened for desired properties, by any of a number of known techniques. Certain of the techniques involve isolating a nucleic acid encoding a polypeptide chain (or portion thereof) of an antigen binding protein of interest (e.g., an anti-KRAS antibody), and manipulating the nucleic acid through recombinant DNA technology. The nucleic acid may be fused to another nucleic acid of interest, or altered (e.g., by mutagenesis or other conventional techniques) to add, delete, or substitute one or more amino acid residues, for example.

Polypeptides of the present disclosure can be produced using any standard methods known in the art. In one example, the polypeptides are produced by recombinant DNA methods by inserting a nucleic acid sequence (a cDNA) encoding the polypeptide into a recombinant expression vector and expressing the DNA sequence under conditions promoting expression.

Nucleic acids encoding any of the various polypeptides disclosed herein may be synthesized chemically. Codon usage may be selected so as to improve expression in a cell. Such codon usage will depend on the cell type selected. Specialized codon usage patterns have been developed for E. coli and other bacteria, as well as mammalian cells, plant cells, yeast cells and insect cells.

General techniques for nucleic acid manipulation are described for example in Sambrook et al., Molecular Cloning: A Laboratory Manual, Vols. 1-3, Cold Spring Harbor Laboratory Press, 2 ed., 1989, or F. Ausubel et al., Current Protocols in Molecular Biology (Green Publishing and Wiley-Interscience: New York, 1987) and periodic updates, herein incorporated by reference. The DNA encoding the polypeptide is operably linked to suitable transcriptional or translational regulatory elements derived from mammalian, viral, or insect genes. Such regulatory elements include a transcriptional promoter, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosomal binding sites, and sequences that control the termination of transcription and translation. The ability to replicate in a host, usually conferred by an origin of replication, and a selection gene to facilitate recognition of transformants is additionally incorporated.

The recombinant DNA can also include any type of protein tag sequence that may be useful for purifying the protein. Examples of protein tags include but are not limited to a histidine tag, a FLAG tag, a myc tag, an HA tag, or a GST tag. Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts can be found in Cloning Vectors: A Laboratory Manual, (Elsevier, N.Y., 1985).

The expression construct is introduced into the host cell using a method appropriate to the host cell. A variety of methods for introducing nucleic acids into host cells are known in the art, including, but not limited to, electroporation; transfection employing calcium chloride, rubidium chloride, calcium phosphate, DEAE-dextran, or other substances; microprojectile bombardment; lipofection; and infection (where the vector is an infectious agent). Suitable host cells include prokaryotes, yeast, mammalian cells, or bacterial cells.

Suitable bacteria include gram negative or gram positive organisms, for example, E. coli or Bacillus spp. Yeast, preferably from the Saccharomyces species, such as S. cerevisiae, may also be used for production of polypeptides. Various mammalian or insect cell culture systems can also be employed to express recombinant proteins. Baculovirus systems for production of heterologous proteins in insect cells are reviewed by Luckow and Summers (1988) Bio/Technology 6:47). Examples of suitable mammalian host cell lines include endothelial cells, COS-7 monkey kidney cells, CV-1, L cells, C127, 3T3, Chinese hamster ovary (CHO), human embryonic kidney cells, HeLa, 293, 293T, and BHK cell lines. Purified polypeptides are prepared by culturing suitable host/vector systems to express the recombinant proteins. For many applications, the small size of many of the polypeptides disclosed herein would make expression in E. coli as the preferred method for expression. The protein is then purified from culture media or cell extracts.

Proteins can also be produced using cell-translation systems. For such purposes the nucleic acids encoding the polypeptide must be modified to allow in vitro transcription to produce mRNA and to allow cell-free translation of the mRNA in the particular cell-free system being utilized (eukaryotic such as a mammalian or yeast cell-free translation system or prokaryotic such as a bacterial cell-free translation system.

KRAS-binding polypeptides can also be produced by chemical synthesis (such as by the methods described in Solid Phase Peptide Synthesis, 2nd ed., 1984, The Pierce Chemical Co., Rockford, Ill.). Modifications to the protein can also be produced by chemical synthesis.

The polypeptides of the present disclosure can be purified by isolation/purification methods for proteins generally known in the field of protein chemistry. Non-limiting examples include extraction, recrystallization, salting out (e.g., with ammonium sulfate or sodium sulfate), centrifugation, dialysis, ultrafiltration, adsorption chromatography, ion exchange chromatography, hydrophobic chromatography, normal phase chromatography, reversed-phase chromatography, gel filtration, gel permeation chromatography, affinity chromatography, electrophoresis, countercurrent distribution or any combinations of these. After purification, polypeptides may be exchanged into different buffers and/or concentrated by any of a variety of methods known to the art, including, but not limited to, filtration and dialysis.

The purified polypeptide is preferably at least 85% pure, more preferably at least 95% pure, and most preferably at least 98% pure. Regardless of the exact numerical value of the purity, the polypeptide is sufficiently pure for use as a pharmaceutical product.

In certain embodiments, the present disclosure provides monoclonal antibodies that bind to KRAS. Monoclonal antibodies may be produced using any technique known in the art, e.g., by immortalizing spleen cells harvested from the transgenic animal after completion of the immunization schedule. The spleen cells can be immortalized using any technique known in the art, e.g., by fusing them with myeloma cells to produce hybridomas. Myeloma cells for use in hybridoma-producing fusion procedures preferably are non-antibody-producing, have high fusion efficiency, and enzyme deficiencies that render them incapable of growing in certain selective media which support the growth of only the desired fused cells (hybridomas). Examples of suitable cell lines for use in mouse fusions include Sp-20, P3-X63/Ag8, P3-X63-Ag8.653, NS1/1.Ag 4 1, Sp210-Ag14, FO, NSO/U, MPC-11, MPC11-X45-GTG 1.7 and S194/5XX0 Bul; examples of cell lines used in rat fusions include R210.RCY3, Y3-Ag 1.2.3, IR983F and 48210. Other cell lines useful for cell fusions are U-266, GM1500-GRG2, LICR-LON-HMy2 and UC729-6.

Antigen-binding fragments of antigen binding proteins of the invention may be produced by conventional techniques known in the art.

Post-Translational Modifications of Antibodies

In certain embodiments, the antibodies (or fragments thereof) of the invention may further comprise post-translational modifications. Exemplary post-translational protein modifications include phosphorylation, acetylation, methylation, ADP-ribosylation, ubiquitination, glycosylation, carbonylation, sumoylation, biotinylation or addition of a polypeptide side chain or of a hydrophobic group. As a result, the modified soluble polypeptides may contain non-amino acid elements, such as lipids, poly- or mono-saccharide, and phosphates. A preferred form of glycosylation is sialylation, which conjugates one or more sialic acid moieties to the polypeptide. Sialic acid moieties improve solubility and serum half-life while also reducing the possible immunogenicity of the protein. See Raju et al. (2001) Biochem. 40(30):8868-76.

In one embodiment, modified forms of the subject soluble polypeptides comprise linking the subject soluble polypeptides to nonproteinaceous polymers. In one embodiment, the polymer is polyethylene glycol (“PEG”), polypropylene glycol, or polyoxyalkylenes, in the manner as set forth in U.S. Pat. No. 4,640,835; 4,496,689; 4,301,144; 4,670,417; 4,791,192 or 4,179,337.

PEG is a water soluble polymer that is commercially available or can be prepared by ring-opening polymerization of ethylene glycol according to methods well known in the art (Sandler and Karo, Polymer Synthesis, Academic Press, New York, Vol. 3, pages 138-161). The term “PEG” is used broadly to encompass any polyethylene glycol molecule, without regard to size or to modification at an end of the PEG, and can be represented by the formula: X—O(CH₂CH₂O)_n—CH₂CH₂OH (1), where n is 20 to 2300 and X is H or a terminal modification, e.g., a C_1-4alkyl. In one embodiment, the PEG of the invention terminates on one end with hydroxy or methoxy, i.e., X is H or CH₃(“methoxy PEG”). A PEG can contain further chemical groups which are necessary for binding reactions; which results from the chemical synthesis of the molecule; or which is a spacer for optimal distance of parts of the molecule. In addition, such a PEG can consist of one or more PEG side-chains which are linked together. PEGs with more than one PEG chain are called multiarmed or branched PEGs. Branched PEGs can be prepared, for example, by the addition of polyethylene oxide to various polyols, including glycerol, pentaerythriol, and sorbitol. For example, a four-armed branched PEG can be prepared from pentaerythriol and ethylene oxide. Branched PEG are described in, for example, EP-A 0 473 084 and U.S. Pat. No. 5,932,462. One form of PEGs includes two PEG side-chains (PEG2) linked via the primary amino groups of a lysine (Monfardini et al. (1995) Bioconjugate Chem. 6:62-69).

The serum clearance rate of PEG-modified polypeptide may be decreased by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or even 90%, relative to the clearance rate of the unmodified binding polypeptide. The PEG-modified polypeptide may have a half-life (t_1/2) which is enhanced relative to the half-life of the unmodified protein. The half-life of PEG-binding polypeptide may be enhanced by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 125%, 150%, 175%, 200%, 250%, 300%, 400% or 500%, or even by 1000% relative to the half-life of the unmodified binding polypeptide. In some embodiments, the protein half-life is determined in vitro, such as in a buffered saline solution or in serum. In other embodiments, the protein half-life is an in vivo half-life, such as the half-life of the protein in the serum or other bodily fluid of an animal

Therapeutic Methods, Formulations and Modes of Administration

Any of the anti-KRAS antibodies or antigen binding fragments disclosed herein may be used in such therapeutic methods. Examples of anti-KRAS antibodies and antigen binding fragments that may be used in the therapeutic methods and compositions of the invention are described above.

In one embodiment, the anti-KRAS antibodies and antibody fragments of the invention are used to treat cancer, particularly cancer associated with detrimental. In one embodiment, the anti-KRAS antibodies and antibody fragments of the invention are used to treat pancreatic cancer. In one embodiment, the anti-KRAS antibodies and antibody fragments of the invention are used to treat lung cancer. In one embodiment, the anti-KRAS antibodies and antibody fragments of the invention are used to treat colorectal cancer.

The present disclosure further provides a method for treating cancer, comprising administering an anti-KRAS antibody or antigen-binding fragment, disclosed herein, including antibodies or fragments comprising the variable regions or CDRs of the heavy and light chains described in Table 4. In one embodiment, the invention provides a method of treating cancer by administering an anti-human KRAS antibody to a subject in need thereof.

Mutant RAS oncogenes have been implicated in about 30 percent of human cancers, and KRAS is its most prominent and aggressive member. Mutant KRAS drives particularly hard-to-treat cancers, including pancreatic, lung, and colorectal cancers. Accordingly, anti-KRAS antibodies and antibody fragments of the invention may be used to treat a subject having cancer which is associated with a KRAS mutation, e.g., a KRAS G12D mutation.

Additional types of cancer that may be treated using anti-KRAS antibodies and fragments of the invention, include, but are not limited to, pancreatic cancer, lung cancer, including non-small cell lung cancer, colorectal cancer, prostate cancer, breast cancer, ovarian cancer, head and neck cancer, bladder cancer, melanoma, colorectal cancer, leiomyoma, leiomyosarcoma, glioma, glioblastoma, esophageal cancer, liver cancer, kidney cancer, stomach cancer, colon cancer, cervical cancer, uterine cancer, liver cancer and a hematological cancer.

In one embodiment, the anti-KRAS antibodies or fragments thereof of the invention are used to treating a subject having pancreatic cancer. Pancreatic cancer is a malignant neoplasm originating from transformed cells arising in tissues forming the pancreas. Pancreatic cancer is one of the most common causes of cancer-related deaths in the world. Due to the absence of specific symptoms, the lack of early detection techniques, and highly aggressive phenotypes, pancreatic cancer is usually diagnosed at an advanced-incurable and metastatic stages. Oncogenic KRAS mutation is the signature genetic event in the progression and growth of pancreatic ductal adenocarcinoma (PDAC), an almost universally fatal disease. Although oncogenic KRAS was first associated with PDAC decades ago, exome sequencing established that KRAS is the most frequently mutated gene in PDAC (95%), the predominant form of pancreatic cancer (90%). The frequency and specific substitutions show cancer type differences, with 98% of KRAS mutations in PDAC occurring at position G12. Of the eight different substitutions found at this position, the predominant substitution is G12D.

In one embodiment, the anti-KRAS antibodies or fragments thereof of the invention are used to treating a subject having lung cancer. In further embodiments, the lung cancer is non small cell lung cancer. Approximately 15-25% of patients with lung adenocarcinoma have tumor associated KRAS mutations. KRAS mutations are uncommon in lung squamous cell carcinoma (Brose et al. (2002) Cancer Res. 62(23):6997-7000). In the majority of cases, these mutations are missense mutations which introduce an amino acid substitution at position 12, 13, or 61. The result of these mutations is constitutive activation of KRAS signaling pathways. In the vast majority of cases, KRAS mutations are found in tumors wild type for EGFR or ALK; in other words, they are non-overlapping with other oncogenic mutations found in NSCLC. Therefore, KRAS mutation defines a distinct molecular subset of the disease.

In one embodiment, the anti-KRAS antibodies or fragments thereof of the invention are used to treating a subject having colorectal cancer. Colorectal cancer (CRC) is the second leading cause of cancer-related death in the United States. The development of CRC is a multistep process characterized by accumulation of genetic alterations that have long been considered to occur in a stepwise process. Along the progression from normal colonic epithelial cells, small adenoma, advanced adenoma, and finally to carcinoma, the KRAS oncogene mutation has a role in a significant proportion of CRCs. KRAS has been reported to be mutated in about 30% of colorectal adenomas and 30% to 50% of CRCs (Russo et al. (2005) Ann Oncol. 16(suppl 4):iv44-iv49; Nosho et al. (2008) PLoS One. 3:e3698).

In one embodiment, the anti-KRAS antibodies or fragments thereof of the invention are used to treating a subject having a precursor lesion. In one embodiment, the anti-KRAS antibodies or fragments thereof of the invention are used to treating a subject having metastatic cancer, including metastatic forms of the aforementioned cancers.

Anti-KRAS antibodies and antibody fragments of the invention can be administered alone or in combination with one or more additional therapies such as chemotherapy radiotherapy, immunotherapy, surgical intervention, for the treatment of cancer. Long-term therapy is equally possible as is adjuvant therapy in the context of other treatment strategies.

Additional agents for treatment can be administered, together (simultaneously) or at different times (sequentially) to the anti-KRAS antibody or antigen binding fragment thereof.

The present disclosure also provides a method of inhibiting growth of a tumor in a subject where an anti-KRAS antibody, or antigen-binding fragment thereof, of the invention is administered to a subject having a tumor.

Further, antibodies and antibody fragments to KRAS described herein can be combined with an immunogenic agent, such as cancerous cells, purified tumor antigens (including recombinant proteins, peptides, and carbohydrate molecules), cells, and cells transfected with genes encoding immune stimulating cytokines (He et al. (2004) J. Immunol. 173:4919-28). Non-limiting examples of tumor vaccines that can be used include peptides of melanoma antigens, such as peptides of gp100, MAGE antigens, Trp-2, MART1 and/or tyrosinase, or tumor cells transfected to express the cytokine GM-CSF (discussed further below).

In certain embodiments, an anti-KRAS antibody or antibody fragment disclosed herein may be combined with a vaccination protocol. Many experimental strategies for vaccination against tumors have been devised. In one of these strategies, a vaccine is prepared using autologous or allogeneic tumor cells. These cellular vaccines have been shown to be most effective when the tumor cells are transduced to express GM-CSF. GM-CSF has been shown to be a potent activator of antigen presentation for tumor vaccination (Dranoff et al. (1993) Proc. Natl. Acad. Sci U.S.A. 90: 3539-43).

The study of gene expression and large scale gene expression patterns in various tumors has led to the definition of so called tumor specific antigens (Rosenberg (1999) Immunity 10: 281-7). In many cases, these tumor specific antigens are differentiation antigens expressed in the tumors and in the cell from which the tumor arose, for example melanocyte antigens gp100, MAGE antigens, and Trp-2. Many of these antigens can be shown to be the targets of tumor specific T cells found in the host. An anti-KRAS antibody or antibody fragment disclosed herein can be used in conjunction with a collection of recombinant proteins and/or peptides expressed in a tumor in order to generate an immune response to these proteins. These proteins are normally viewed by the immune system as self antigens and are therefore tolerant to them. The tumor antigen can include the protein telomerase, which is required for the synthesis of telomeres of chromosomes and which is expressed in more than 85% of human cancers and in only a limited number of somatic tissues (Kim et al. (1994) Science 266: 2011-2013). (These somatic tissues may be protected from immune attack by various means). Tumor antigen can also be “neo-antigens” expressed in cancer cells because of somatic mutations that alter protein sequence or create fusion proteins between two unrelated sequences (i.e., bcr-abl in the Philadelphia chromosome), or idiotype from B cell tumors.

Other tumor vaccines can include the proteins from viruses implicated in human cancers such a Human Papilloma Viruses (HPV), Hepatitis Viruses (HBV and HCV) and Kaposi's Herpes Sarcoma Virus (KHSV). Another form of tumor specific antigen which can be used in conjunction with an anti-KRAS antibody or antibody fragment disclosed herein is purified heat shock proteins (HSP) isolated from the tumor tissue itself. These heat shock proteins contain fragments of proteins from the tumor cells and these HSPs are highly efficient at delivery to antigen presenting cells for eliciting tumor immunity (Suot & Srivastava (1995) Science 269:1585-1588; Tamura et al. (1997) Science 278:117-120).

Dendritic cells (DC) are potent antigen presenting cells that can be used to prime antigen-specific responses. DC's can be produced ex vivo and loaded with various protein and peptide antigens as well as tumor cell extracts (Nestle et al. (1998) Nature Medicine 4: 328-332). DCs can also be transduced by genetic means to express these tumor antigens as well. DCs have also been fused directly to tumor cells for the purposes of immunization (Kugler et al. (2000) Nature Medicine 6:332-336). As a method of vaccination, DC immunization can be effectively combined with KRAS blockade to activate more potent anti-tumor responses.

An anti-KRAS antibody or antibody fragment disclosed herein can also be combined with other cancer treatments. An anti-KRAS antibody or antibody fragment disclosed herein can be effectively combined with chemotherapeutic regimes. In these instances, it may be possible to reduce the dose of chemotherapeutic reagent administered (Mokyr et al. (1998) Cancer Research 58: 5301-5304). An example of such a combination is an anti-KRAS antibody in combination with decarbazine for the treatment of melanoma. Another example of such a combination is an anti-KRAS antibody in combination with interleukin-2 (IL-2) for the treatment of melanoma. The scientific rationale behind the combined use of KRAS blockade and chemotherapy is that cell death, that is a consequence of the cytotoxic action of most chemotherapeutic compounds, should result in increased levels of tumor antigen in the antigen presentation pathway. Other combination therapies that may result in synergy with an anti-KRAS antibody or antibody fragment disclosed herein through cell death are radiation, surgery, and hormone deprivation. Each of these protocols creates a source of tumor antigen in the host. Angiogenesis inhibitors can also be combined with an anti-KRAS antibody or antibody fragment disclosed herein. Inhibition of angiogenesis often leads to tumor cell death which may feed tumor antigens into host antigen presentation pathways.

In some embodiments, the anti-KRAS antibodies and antibody fragments of the invention may be administered in conjunction with a chemotherapy or chemotherapeutic agent. In some embodiments, the anti-KRAS antibodies and antibody fragments of the invention may be administered in conjunction with a radiation therapy or radiotherapeutic agent. In some embodiments, the anti-KRAS antibodies and antibody fragments of the invention may be administered in conjunction with a targeted therapy or targeted therapeutic agent. In some embodiments, the anti-KRAS antibodies and antibody fragments of the invention may be administered in conjunction with an immunotherapy or immunotherapeutic agent, for example a monoclonal antibody.

In certain embodiments of such methods, one or more anti-KRAS antibodies and antibody fragments of the invention can be administered, together (simultaneously) or at different times (sequentially). In addition, anti-KRAS antibodies and antibody fragments of the invention can be administered with another type of compound(s) for treating cancer or for inhibiting angiogenesis.

The disclosed human anti-KRAS antibodies can be co-administered with one or other more therapeutic agents, e.g., a cytotoxic agent, a radiotoxic agent or an immunosuppressive agent. The antibody can be linked to the agent (as an immuno-complex) or can be administered separate from the agent. In the latter case (separate administration), the antibody can be administered before, after or concurrently with the agent or can be co-administered with other known therapies, e.g., an anti-cancer therapy, e.g., radiation. Such therapeutic agents include, among others, anti-neoplastic agents such as doxorubicin (adriamycin), cisplatin bleomycin sulfate, carmustine, chlorambucil, dacarbazine and cyclophosphamide hydroxyurea which, by themselves, are only effective at levels which are toxic or subtoxic to a patient. Cisplatin is intravenously administered as a 100 mg/ml dose once every four weeks and adriamycin is intravenously administered as a 60-75 mg/ml dose once every 21 days. Co-administration of the anti-KRAS antibodies and antibody fragments of the invention, with chemotherapeutic agents provides two anti-cancer agents which operate via different mechanisms which yield a cytotoxic effect to human tumor cells. Such co-administration can solve problems due to development of resistance to drugs or a change in the antigenicity of the tumor cells which would render them unreactive with the antibody.

Bispecific antibodies can be used to target two separate antigens. For example anti-Fc receptor/anti-tumor antigen (e.g., Her-2/neu) bispecific antibodies have been used to target macrophages to sites of tumor. This targeting may more effectively activate tumor specific responses. The T cell arm of these responses would be augmented by the use of an anti-KRAS antibody or antibody fragment disclosed herein. Alternatively, antigen may be delivered directly to DCs by the use of bispecific antibodies which bind to tumor antigen and a dendritic cell specific cell surface marker.

Anti-KRAS antibodies or antibody fragments disclosed herein can also be used in combination with bispecific antibodies that target, for example, Fcα or Fcγ receptor-expressing effectors cells to tumor cells (U.S. Pat. Nos. 5,922,845 and 5,837,243).

Tumors evade host immune surveillance by a large variety of mechanisms. Many of these mechanisms may be overcome by the inactivation of proteins which are expressed by the tumors and which are immunosuppressive. These include among others TGF-β (Kehrl et al. (1986) J. Exp. Med. 163: 1037-1050), IL-10 (Howard & O'Garra (1992) Immunology Today 13: 198-200), and Fas ligand (Hahne et al. (1996) Science 274: 1363-1365). Antibodies to each of these entities can be used in combination with anti-KRAS antibodies and antibody fragments described herein to counteract the effects of the immunosuppressive agent and favor tumor immune responses by the host.

Suitable routes of administering the antibody compositions described herein (e.g., human monoclonal antibodies, multispecific and bispecific molecules and immunoconjugates) are in vivo and in vitro are well known in the art and can be selected by those of ordinary skill. For example, the antibody compositions can be administered by injection (e.g., intravenous or subcutaneous). Suitable dosages of the molecules used will depend on the age and weight of the subject and the concentration and/or formulation of the antibody composition.

Techniques and dosages for administration vary depending on the type of specific binding protein and the specific condition being treated but can be readily determined by the skilled artisan. In general, regulatory agencies require that a protein reagent to be used as a therapeutic is formulated so as to have acceptably low levels of pyrogens. Accordingly, therapeutic formulations will generally be distinguished from other formulations in that they are substantially pyrogen free, or at least contain no more than acceptable levels of pyrogen as determined by the appropriate regulatory agency (e.g., FDA).

Therapeutic compositions comprising the antigen binding proteins of the present disclosure may be administered with a pharmaceutically acceptable diluent, carrier, or excipient, in unit dosage form. Administration may be parenteral (e.g., intravenous, subcutaneous), oral, or topical, as non-limiting examples. In addition, any gene therapy technique, using nucleic acids encoding the polypeptides of the invention, may be employed, such as naked DNA delivery, recombinant genes and vectors, cell-based delivery, including ex vivo manipulation of patients' cells, and the like.

Thus, an anti-KRAS antibody, or antigen binding portion thereof, of the invention can be incorporated into a pharmaceutical composition suitable for parenteral administration. Preferably, the anti-KRAS antibody, or antigen binding portion thereof, will be prepared as an injectable solution containing 0.1-250 mg/ml antibody. The injectable solution can be composed of either a liquid or lyophilized dosage form in a flint or amber vial, ampoule or pre-filled syringe. The buffer can be L-histidine (1-50 mM), optimally 5-10 mM, at pH 5.0 to 7.0 (optimally pH 6.0). Other suitable buffers include but are not limited to, sodium succinate, sodium citrate, sodium phosphate or potassium phosphate. Sodium chloride can be used to modify the toxicity of the solution at a concentration of 0-300 mM (optimally 150 mM for a liquid dosage form). Cryoprotectants can be included for a lyophilized dosage form, principally 0-10% sucrose (optimally 0.5-1.0%). Other suitable cryoprotectants include trehalose and lactose. Bulking agents can be included for a lyophilized dosage form, principally 1-10% mannitol (optimally 2-4%). Stabilizers can be used in both liquid and lyophilized dosage forms, principally 1-50 mM L-methionine (optimally 5-10 mM). Other suitable bulking agents include glycine, arginine, can be included as 0-0.05% polysorbate-80 (optimally 0.005-0.01%). Additional surfactants include but are not limited to polysorbate 20 and BRIJ surfactants.

The compositions of this invention may be in a variety of forms. These include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (e.g., injectable and infusible solutions), dispersions or suspensions, tablets, pills, powders, liposomes and suppositories. The preferred form depends on the intended mode of administration and therapeutic application. Typical preferred compositions are in the form of injectable or infusible solutions, such as compositions similar to those used for passive immunization of humans with other antibodies. The preferred mode of administration is parenteral (e.g., intravenous, subcutaneous, intraperitoneal, intramuscular). In a preferred embodiment, an anti-KRAS antibody, or antigen binding portion thereof, described herein is administered by intravenous infusion or injection. In another preferred embodiment, an anti-KRAS antibody, or antigen binding portion thereof, is administered by intramuscular or subcutaneous injection.

Therapeutic compositions typically must be sterile and stable under the conditions of manufacture and storage. The composition can be formulated as a solution, microemulsion, dispersion, liposome, or other ordered structure suitable to high drug concentration. Sterile injectable solutions can be prepared by incorporating the active compound (i.e., antibody or antibody portion) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile, lyophilized powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and spray-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof. The proper fluidity of a solution can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. Prolonged absorption of injectable compositions can be brought about by including, in the composition, an agent that delays absorption, for example, monostearate salts and gelatin.

The anti-KRAS antibody, or antigen binding portion thereof, of the present invention can be administered by a variety of methods known in the art, although for many therapeutic applications, the preferred route/mode of administration is subcutaneous injection, intravenous injection, or infusion. As will be appreciated by the skilled artisan, the route and/or mode of administration will vary depending upon the desired results. In certain embodiments, the active compound may be prepared with a carrier that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Many methods for the preparation of such formulations are patented or generally known to those skilled in the art. See, e.g., Sustained and Controlled Release Drug Delivery Systems, J. R. Robinson, ed., (Marcel Dekker, Inc., New York, 1978).

A therapeutically effective dose refers to a dose that produces the therapeutic effects for which it is administered. The exact dose will depend on the disorder to be treated, and may be ascertained by one skilled in the art using known techniques. In general, the anti-KRAS antibody, or fragment thereof, is administered at about 0.01 μg/kg to about 50 mg/kg per day, preferably 0.01 mg/kg to about 30 mg/kg per day, most preferably 0.1 mg/kg to about 20 mg/kg per day. The polypeptide may be given daily (e.g., once, twice, three times, or four times daily) or preferably less frequently (e.g., weekly, every two weeks, every three weeks, monthly, or quarterly). In addition, as is known in the art, adjustments for age as well as the body weight, general health, sex, diet, time of administration, drug interaction, and the severity of the disease may be necessary.

In certain embodiments, the subject anti-KRAS antibodies or antibody fragments of the invention can be used alone.

Diagnostics and Kits

In certain embodiments, any of the anti-KRAS antibodies (or fragments) provided herein are useful for detecting the presence of KRAS in vitro, e.g., in a biological sample, or in vivo. Such detection methods using the anti-KRAS antibodies (or fragments) disclosed herein may be used for diagnostic purpose. Exemplary disorders that may be diagnosed using an antibody of the invention include cancer.

The antibodies and fragments of the invention may be used to detect the presence of KRAS in a biological sample. In certain embodiments, the method comprises contacting the biological sample with an anti-KRAS antibody (or fragment) as described herein under conditions permissive for binding of the anti-KRAS antibody to KRAS, and detecting whether a complex is formed between the anti-KRAS antibody and KRAS. Such method may be an in vitro or in vivo method. In one embodiment, an anti-KRAS antibody is used to select subjects eligible for therapy with an anti-KRAS antibody, e.g. where KRAS is a biomarker for selection of patients. A biological sample may be a cell or tissue, such as a sample of a tumor (e.g., pancreatic, lung or colorectal).

In certain embodiments, the binding polypeptides of fragments thereof can be labeled or unlabeled for diagnostic purposes. Typically, diagnostic assays entail detecting the formation of a complex resulting from the binding of an antibody or fragment to KRAS. The binding polypeptides or fragments can be directly labeled, similar to antibodies. A variety of labels can be employed, including, but not limited to, radionuclides, fluorescers, enzymes, enzyme substrates, enzyme cofactors, enzyme inhibitors and ligands (e.g., biotin, haptens). Numerous appropriate immunoassays are known to the skilled artisan (see, for example, U.S. Pat. Nos. 3,817,827; 3,850,752; 3,901,654; and 4,098,876). When unlabeled, the binding polypeptides can be used in assays, such as agglutination assays. Unlabeled binding polypeptides can also be used in combination with another (one or more) suitable reagent which can be used to detect the binding polypeptide, such as a labeled antibody reactive with the binding polypeptide or other suitable reagent (e.g., labeled protein A).

In one embodiment, the binding polypeptides of the present disclosure can be utilized in enzyme immunoassays, wherein the subject polypeptides are conjugated to an enzyme. When a biological sample comprising a KRAS protein is combined with the subject binding polypeptides, binding occurs between the binding polypeptides and the KRAS protein. In one embodiment, a sample containing cells expressing a KRAS protein (e.g., endothelial cells) is combined with the subject antibodies, and binding occurs between the binding polypeptides and cells bearing a KRAS protein recognized by the binding polypeptide. These bound cells can be separated from unbound reagents and the presence of the binding polypeptide-enzyme conjugate specifically bound to the cells can be determined, for example, by contacting the sample with a substrate of the enzyme which produces a color or other detectable change when acted on by the enzyme. In another embodiment, the subject binding polypeptides can be unlabeled, and a second, labeled polypeptide (e.g., an antibody) can be added which recognizes the subject binding polypeptide.

In certain aspects, kits for use in detecting the presence of a KRAS protein in a biological sample using the antibodies or fragments thereof of the invention can also be prepared. Such kits will include a KRAS binding polypeptide, e.g., antibodies or fragments thereof, which binds to a KRAS protein or portion of said receptor, as well as one or more ancillary reagents suitable for detecting the presence of a complex between the binding polypeptide and the receptor protein or portions thereof. The polypeptide compositions of the present invention can be provided in lyophilized form, either alone or in combination with additional antibodies specific for other epitopes. The binding polypeptides and/or antibodies, which can be labeled or unlabeled, can be included in the kits with adjunct ingredients (e.g., buffers, such as Tris, phosphate and carbonate, stabilizers, excipients, biocides and/or inert proteins, e.g., bovine serum albumin) For example, the binding polypeptides and/or antibodies can be provided as a lyophilized mixture with the adjunct ingredients, or the adjunct ingredients can be separately provided for combination by the user. Generally, these adjunct materials will be present in less than about 5% weight based on the amount of active binding polypeptide or antibody, and usually will be present in a total amount of at least about 0.001% weight based on polypeptide or antibody concentration. Where a second antibody capable of binding to the binding polypeptide is employed, such antibody can be provided in the kit, for instance in a separate vial or container. The second antibody, if present, is typically labeled, and can be formulated in an analogous manner with the antibody formulations described above.

Other embodiments are described in the following non-limiting Examples.

EXAMPLES
Example 1. Identification of Human Anti-KRAS Antibodies

Recombinant human antibodies specific for human KRAS were identified and selected for therapeutic characteristics, including specificity for human KRAS and a high affinity for KRAS (e.g., at least 10⁻⁶M). Affinity data for antibodies 1E3, 4E10, 5C5 and 5F8 are shown below in Table 1.

TABLE 1

Rmax
Chi²

ka (1/Ms)
kd (1/s)
KD (M)
(RU)
(RU²)
U-value

1E3
2.69E+05
0.00113
4.20E−09
9.971
0.525
7

4E10
1.35E+05
0.001299
9.60E−09
10.14
0.232
5

5C5
1.66E+05
0.001099
6.63E−09
9.389
0.74
9

5F8
1.82E+05
0.002285
1.26E−08
11.98
0.287
4

The amino acid sequences of the heavy and light chain variable domains of the identified anti-KRAS antibodies, and their complementarity determining regions (CDRs), are described in Table 2, below.

TABLE 2

Antibody Amino Acid Sequences

Heavy chain
Light chain

variable domain regions
variable domain regions

K3-1F4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSLNAHWVFGGGTKLTVL

S
SEQ ID NO. 2

SEQ ID NO. 1

K3-1F4
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 75
SEQ ID NO. 78

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 76
SEQ ID NO. 79

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLNAHWV

SEQ ID NO. 77
SEQ ID NO. 80

K3-1A7
QVQLVESGGGVVQPGRSLRLSCTNSGFSF
DIVMTQSPSTLSASVGDRVTITCRASQSI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

SSWLAWYQQKPGKAPKVLIYKASSLESGV

YYADSVKGRFTISRDNSKNTLYLHMNSLR
PSRFSGSGSGTEFTLTISSLQPDDFAAYY

AEDTAVYYCASGGNYYGSGTIVSHGLDFW
CQHYNSYPYTFGQGTKLEIK

GQGTTVTVSS
SEQ ID NO. 4

SEQ ID NO. 3

K3-1A7
HC CDR1
LC CDR1

GFSFSGYAMH
RASQSISSWLA

SEQ ID NO. 81
SEQ ID NO. 84

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
KASSLES

SEQ ID NO. 82
SEQ ID NO. 85

HC CDR3
LC CDR3

GGNYYGSGTIVSHGLDF
QHYNSYPYT

SEQ ID NO. 83
SEQ ID NO. 86

K3-2B2
QVQLVESGGGVVQPGRSLRLSCTNSGFSF
SSELTQDPAVSVALGQTVRITCQGDSLRS

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

YYASWYQQKPGQAPVLVIYGKNNRPSGIP

YYADSVKGRFTISRDNSKNTLYLHMNSLR
DRFSGSSSGNTASLTITGAQAEDEADYYC

AEDTAVYYCASGGNYYGSGTIVSHGMDVW

NSRDSSGNHRGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 6

SEQ ID NO. 5

K3-2B2
HC CDR1
LC CDR1

GFSFSGYAMH
QGDSLRSYYAS

SEQ ID NO. 87
SEQ ID NO. 90

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
GKNNRPS

SEQ ID NO. 88
SEQ ID NO. 91

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
NSRDSSGNH

SEQ ID NO. 89
SEQ ID NO. 92

K3-2C2
QVQLVESGGGVVQPGRSLRLSCSNSGFSF
DIVMTQSPSSLSASVGDRVTITCRASQSI

SGYTMHWVRQAPGKGLEWVAVISFDGSHK

SNYLNWYQQKPGKAPKLLIYAASSLQSGV

YYADSVKGRFTISRDNSKNTLYLHMNSLR
PSRFSGSGSGTDFTLTISSLQPEDFATYY

AEDTAVYYCAKKMHYGSGAYHFDLWGQGT
CQQSYSSPFTFGPGTKVDIK

LVTVSS
SEQ ID NO. 8

SEQ ID NO. 7

K3-2C2
HC CDR1
LC CDR1

GFSFSGYTMH
RASQSISNYLN

SEQ ID NO. 93
SEQ ID NO. 96

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
AASSLQS

SEQ ID NO. 94
SEQ ID NO. 97

HC CDR3
LC CDR3

KMHYGSGAYHFDL
QQSYSSPFT

SEQ ID NO. 95
SEQ ID NO. 98

K3-2H8
EVQLLESGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYNYVSWYQQHPGKAPKLMIYDVSNRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLT
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTSSSTLVVFGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 10

SEQ ID NO. 9

K3-2H8
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDVGGYNYVS

SEQ ID NO. 99
SEQ ID NO. 102

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSNRPS

SEQ ID NO. 100
SEQ ID NO. 103

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTSSSTLVV

SEQ ID NO. 101
SEQ ID NO. 104

K3-3E8
EVQLLEPGGGVVQPGRSLRLSCTNSGFSF
QSALTQPRSVSGSPGQSVTISCTGTSSNV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYNHVSWYQQHPGKAPKVIIYDVNKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLR
GVSHRFSGSKSANTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTTSSTYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 12

SEQ ID NO. 11

K3-3E8
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSNVGGYNHVS

SEQ ID NO. 105
SEQ ID NO. 108

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVNKRPS

SEQ ID NO. 106
SEQ ID NO. 109

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTTSSTYV

SEQ ID NO. 107
SEQ ID NO. 110

K3-4D9
QVQLVESAGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYKYVSWYQQYPGKAPKLMIYDVSKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLT
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCNSYTSSRIYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 14

SEQ ID NO. 13

K3-4D9
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDVGGYKYVS

SEQ ID NO. 111
SEQ ID NO. 114

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSKRPS

SEQ ID NO. 112
SEQ ID NO. 115

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
NSYTSSRIYV

SEQ ID NO. 113
SEQ ID NO. 116

K3-4F10
EVQLLEPGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSNDI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GAYNYVSWYQQHPGKAPKLMIYDVNNRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLR
GVPDRFSGSKSGNMASLTISGLQAEDDAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTSSSTLVVFGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 16

SEQ ID NO. 15

K3-4F10
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSNDIGAYNYVS

SEQ ID NO. 117
SEQ ID NO. 120

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVNNRPS

SEQ ID NO. 118
SEQ ID NO. 121

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTSSSTLVV

SEQ ID NO. 119
SEQ ID NO. 122

K3-5H6
QVQLVQSGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGSNWVSWYQQHPGKAPKLMIYDVSKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSVR
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNHYGSGTIVSHGMDVR
YYCSSYTSSSTYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 18

SEQ ID NO. 17

K3-5H6
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDIGGSNWVS

SEQ ID NO. 123
SEQ ID NO. 126

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSKRPS

SEQ ID NO. 124
SEQ ID NO. 127

HC CDR3
LC CDR3

GGNHYGSGTIVSHGMDV
SSYTSSSTYV

SEQ ID NO. 125
SEQ ID NO. 128

K5-1F12
QVQLVESGGGLVQPGGSLRLSCAASGFTF
QAGLTQPASVSGSPGQSITISCTGTSSDV

SSYWMSWVRQAPGKGLEWVGFIRSKAYGG

GGYNYVSWYQQHPGKAPKLMIYDVSKRPS

TTEYAASVKGRFTISRDDSKSIAYLQMNS
GVSNRFSGSKSGNTASLTISGLQAEDEAD

LKTEDTAVYYCTRDGGSYFDYWGQGTLVT
YYCSSYTSSSTYVFGTGTKVTVL

VSS
SEQ ID NO. 20

SEQ ID NO. 19

K5-1F12
HC CDR1
LC CDR1

GFTFSSYWMS
TGTSSDVGGYNYVS

SEQ ID NO. 129
SEQ ID NO. 132

HC CDR2
LC CDR2

FIRSKAYGGTTEYAASVKG
DVSKRPS

SEQ ID NO. 130
SEQ ID NO. 133

HC CDR3
LC CDR3

DGGSYFDY
SSYTSSSTYV

SEQ ID NO. 131
SEQ ID NO. 134

Example 2. Affinity Maturation

Affinity maturation was performed on the anti-hKRAS antibodies described in Example 1. The amino acid sequences of the heavy and light chain variable domains of the affinity matured anti-KRAS antibodies, and their CDRs, are described in Table 3. To improve the affinity of the anti-KRAS antibodies, affinity maturation was carried out using site specific random mutagenesis. A germline hotspot mutagenesis method was used, using PCR and phage display, as described in. Ho and Pastan, (2009) Methods Mol Biol. 525:293-30, incorporated by reference in its entirety herein. Briefly, the steps were as follows:

1—Sequence analysis of clone K3-1F4 was performed to determine germline hotspot(s). Germline hotspots were identified in the heavy chain CDR1 (HCDR1) and the light chain CDR3 (LCDR);

2—Overlap PCR was performed to randomize residues in HCDR1(FTS XXX GMH) and LCDR3 (WDD XXXX HWV) with the following oligonucleotides:

SfiI-VH-F

5′-cgcggcccagccggccatggcagagGTGCA-3′

VL-SfiI-R

5′-CCAGGCCCCCGAGGCCCAGGACGGTCAGCT-3′

HCDR1-NNK-R

5′-GACCCAATGCATGCCMNNMNNMNNGGAGGTGAAT-3′

HCDR1-F

5′-GGCATGCATTGGGTCCGCCA-3′

LCDR3-R

5′-GTCATCCCATGCTGCACAGT-3′

LCDR3-NNK-F

5′-GCAGCATGGGATGACnnknnknnknnkCATTGGGTGT-3′

3—The PCR product was digested with restriction enzyme Sfi I and ligated into the pCGMT3 vector;

4—The recombinant vector was ransformed into SS320 electroporation-competent E. coli cells;

5—The resulting library size was 6×10⁶; and

6—Five (5) rounds of panning were performed.

Another library was made for affinity maturation, where some residues in the heavy chain CDR3 (HCDR3) were randomized with the following oligonucleotides:

HCDR3-R

5′-TGTCGCACAGTAATACACAGCCGTGTCCTC-3′

HCDR3-NNK-F

5′-TATTACTGTGCGACAnnknnknnknnknnkATGGACCTCT-3′

The resultant library size was 3×10⁷. From this library, 3 clones were identified: (1F4_5H1, 1F4_5E2 and 1F4_5F2) and their sequences provided in Table 3.

TABLE 3

Heavy chain
Light chain

variable domain regions
variable domain regions

1F4_1H2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SLNGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYGSTHWVFGGGTKLTVL

S
SEQ ID NO. 22

SEQ ID NO. 21

1F4_1H2
HC CDR1
LC CDR1

GFTSSLNGMH
SGSNSNIGKNYVS

SEQ ID NO. 135
SEQ ID NO. 138

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 136
SEQ ID NO. 139

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYGSTHWV

SEQ ID NO. 137
SEQ ID NO. 140

1F4_1C3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RQYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDGRKVHWVFGGGTKLTVL

S
SEQ ID NO. 24

SEQ ID NO. 23

1F4_1C3
HC CDR1
LC CDR1

GFTSRQYGMH
SGSNSNIGKNYVS

SEQ ID NO. 141
SEQ ID NO. 144

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 142
SEQ ID NO. 145

HC CDR3
LC CDR3

SLYSSMDL
AAWDDGRKVHWV

SEQ ID NO. 143
SEQ ID NO. 146

1F4_1D3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

STYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSRTTHWVFGGGTKLTVL

S
SEQ ID NO. 26

SEQ ID NO. 25

1F4_1D3
HC CDR1
LC CDR1

GFTSSTYGMH
SGSNSNIGKNYVS

SEQ ID NO. 147
SEQ ID NO. 150

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 148
SEQ ID NO. 151

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSRTTHWV

SEQ ID NO. 149
SEQ ID NO. 152

1F4_1E6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RPYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDFHSEHWVFGGGTKLTVL

S
SEQ ID NO. 28

SEQ ID NO. 27

1F4_1E6
HC CDR1
LC CDR1

GFTSRPYGMH
SGSNSNIGKNYVS

SEQ ID NO. 153
SEQ ID NO. 156

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 154
SEQ ID NO. 157

HC CDR3
LC CDR3

SLYSSMDL
AAWDDFHSEHWV

SEQ ID NO. 155
SEQ ID NO. 158

1F4_1F6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

ATYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSSDTHWVFGGGTKLTVL

S
SEQ ID NO. 30

SEQ ID NO. 29

1F4_1F6
HC CDR1
LC CDR1

GFTSATYGMH
SGSNSNIGKNYVS

SEQ ID NO. 159
SEQ ID NO. 162

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 160
SEQ ID NO. 163

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSSDTHWV

SEQ ID NO. 161
SEQ ID NO. 164

1F4_1G6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SFHGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSGDVHWVFGGGTKLTVL

S
SEQ ID NO. 32

SEQ ID NO. 31

1F4_1G6
HC CDR1
LC CDR1

GFTSSFHGMH
SGSNSNIGKNYVS

SEQ ID NO. 165
SEQ ID NO. 168

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 166
SEQ ID NO. 169

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSGDVHWV

SEQ ID NO. 167
SEQ ID NO. 170

1F4_1E3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYRGPHWVFGGGTKLTVL

S
SEQ ID NO. 34

SEQ ID NO. 33

1F4_1E3
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 171
SEQ ID NO. 174

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 172
SEQ ID NO. 175

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYRGPHWV

SEQ ID NO. 173
SEQ ID NO. 176

1F4_3D11
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYRGPHWVFGGGTKLTVL

S
SEQ ID NO. 36

SEQ ID NO. 35

1F4_3D11
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 177
SEQ ID NO. 180

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 178
SEQ ID NO. 181

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYRGPHWV

SEQ ID NO. 179
SEQ ID NO. 182

1F4_4E10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RAPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDHNGEHWVFGGGTKLTVL

S
SEQ ID NO. 38

SEQ ID NO. 37

1F4_4E10
HC CDR1
LC CDR1

GFTSRAPGMH
SGSNSNIGKNYVS

SEQ ID NO. 183
SEQ ID NO. 186

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 184
SEQ ID NO. 187

HC CDR3
LC CDR3

SLYSSMDL
AAWDDHNGEHWV

SEQ ID NO. 185
SEQ ID NO. 188

1F4_4F10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDKFGVHWVFGGGTKLTVL

S
SEQ ID NO. 40

SEQ ID NO. 39

1F4_4F10
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 189
SEQ ID NO. 192

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 190
SEQ ID NO. 193

HC CDR3
LC CDR3

SLYSSMDL
AAWDDKFGVHWV

SEQ ID NO. 191
SEQ ID NO. 194

1F4_4A12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSPTIHWVFGGGTKLTVL

S
SEQ ID NO. 42

SEQ ID NO. 41

1F4_4A12
HC CDR1
LC CDR1

GFTSRKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 195
SEQ ID NO. 198

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 196
SEQ ID NO. 199

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSPTIHWV

SEQ ID NO. 197
SEQ ID NO. 200

1F4_4D12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNFNI

HNKGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDFAGVHWVFGGGTKLTVL

S
SEQ ID NO. 44

SEQ ID NO. 43

1F4_4D12
HC CDR1
LC CDR1

GFTSHNKGMH
SGSNFNIGKNYVS

SEQ ID NO. 201
SEQ ID NO. 204

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 202
SEQ ID NO. 205

HC CDR3
LC CDR3

SLYSSMDL
AAWDDFAGVHWV

SEQ ID NO. 203
SEQ ID NO.206

1F4_4E12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

YKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCASSLYSSMDLWGQGTTVTVS
YCAAWDDSFSEHWVFGGGTKLTVL

S
SEQ ID NO. 46

SEQ ID NO. 45

1F4_4E12
HC CDR1
LC CDR1

GFTSYKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 207
SEQ ID NO. 210

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 208
SEQ ID NO. 211

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSFSEHWV

SEQ ID NO. 209
SEQ ID NO. 212

1F4_5C4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RAPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDQNGVHWVFGGGTKLTVL

S
SEQ ID NO. 48

SEQ ID NO. 47

1F4_5C4
HC CDR1
LC CDR1

GFTSRAPGMH
SGSNSNIGKNYVS

SEQ ID NO. 213
SEQ ID NO. 216

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 214
SEQ ID NO. 217

HC CDR3
LC CDR3

SLYSSMDL
AAWDDQNGVHWV

SEQ ID NO. 215
SEQ ID NO. 218

1F4_5A4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RSPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLRGVHWVFGGGTKLTVL

S
SEQ ID NO. 50

SEQ ID NO. 49

1F4_5A4
HC CDR1
LC CDR1

GFTSRSPGMH
SGSNSNIGKNYVS

SEQ ID NO. 219
SEQ ID NO. 222

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 220
SEQ ID NO. 223

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLRGVHWV

SEQ ID NO. 221
SEQ ID NO. 224

1F4_5B7
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHHGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDRHGTHWVFGGGTKLTVL

S
SEQ ID NO. 52

SEQ ID NO. 51

1F4_5B7
HC CDR1
LC CDR1

GFTSRHHGMH
SGSNSNIGKNYVS

SEQ ID NO. 225
SEQ ID NO. 228

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 226
SEQ ID NO. 229

HC CDR3
LC CDR3

SLYSSMDL
AAWDDRHGTHWV

SEQ ID NO.227
SEQ ID NO. 230

1F4_5F8
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RNPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSTGVHWVFGGGTKLTVL

S
SEQ ID NO. 54

SEQ ID NO. 53

1F4_5F8
HC CDR1
LC CDR1

GFTSRNPGMH
SGSNSNIGKNYVS

SEQ ID NO. 231
SEQ ID NO. 234

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 232
SEQ ID NO. 235

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSTGVHWV

SEQ ID NO. 233
SEQ ID NO. 236

1F4_5D3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RTYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLPTDHWVFGGGTKLTVL

S
SEQ ID NO. 56

SEQ ID NO. 55

1F4_5D3
HC CDR1
LC CDR1

GFTSRTYGMH
SGSNSNIGKNYVS

SEQ ID NO. 237
SEQ ID NO. 240

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 238
SEQ ID NO. 241

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLPTDHWV

SEQ ID NO. 239
SEQ ID NO. 242

1F4_5G5
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RQYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYSGVHWVFGGGTKLTVL

S
SEQ ID NO. 58

SEQ ID NO. 57

1F4_5G5
HC CDR1
LC CDR1

GFTSRQYGMH
SGSNSNIGKNYVS

SEQ ID NO. 243
SEQ ID NO. 246

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 244
SEQ ID NO. 247

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYSGVHWV

SEQ ID NO. 245
SEQ ID NO. 248

1F4_5A10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SPYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDNPRDHWVFGGGTKLTVL

S
SEQ ID NO. 60

SEQ ID NO. 59

1F4_5A10
HC CDR1
LC CDR1

GFTSSPYGMH
SGSNSNIGKNYVS

SEQ ID NO. 249
SEQ ID NO. 252

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 250
SEQ ID NO. 253

HC CDR3
LC CDR3

SLYSSMDL
AAWDDNPRDHWV

SEQ ID NO. 251
SEQ ID NO. 254

1F4_5B12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SKPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLRGVHWVFGGGTKLTVL

S
SEQ ID NO. 62

SEQ ID NO. 61

1F4_5B12
HC CDR1
LC CDR1

GFTSSKPGMH
SGSNSNIGKNYVS

SEQ ID NO. 255
SEQ ID NO. 258

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 256
SEQ ID NO. 259

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLRGVHWV

SEQ ID NO. 257
SEQ ID NO. 260

1F4_5C5
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

KKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLGGDHWVFGGGTKLTVL

S
SEQ ID NO. 64

SEQ ID NO. 63

1F4_5C5
HC CDR1
LC CDR1

GFTSKKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 261
SEQ ID NO. 264

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 262
SEQ ID NO. 265

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLGGDHWV

SEQ ID NO. 263
SEQ ID NO. 266

1F4_5F6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

TLPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSAGVHWVFGGGTKLTVL

S
SEQ ID NO. 66

SEQ ID NO. 65

1F4_5F6
HC CDR1
LC CDR1

GFTSTLPGMH
SGSNSNIGKNYVS

SEQ ID NO. 267
SEQ ID NO. 270

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 268
SEQ ID NO. 271

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSAGVHWV

SEQ ID NO. 269
SEQ ID NO. 272

1F4_5H4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

KMPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDEHGVHWVFGGGTKLTVL

S
SEQ ID NO. 68

SEQ ID NO. 67

1F4_5H4
HC CDR1
LC CDR1

GFTSKMPGMH
SGSNSNIGKNYVS

SEQ ID NO. 273
SEQ ID NO. 276

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 274
SEQ ID NO. 277

HC CDR3
LC CDR3

SLYSSMDL
AAWDDEHGVHWV

SEQ ID NO. 275
SEQ ID NO. 278

1F4_5H1
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCAASLYSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S
SEQ ID NO. 70

SEQ ID NO. 69

1F4_5H1
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 279
SEQ ID NO. 282

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 280
SEQ ID NO. 283

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLSAHWV

SEQ ID NO. 281
SEQ ID NO. 284

1F4_5E2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSMVSSMDLWGQGTTVTVS
YCAAWDDSLSTHWVFGGGTKLTVL

S
SEQ ID NO. 72

SEQ ID NO. 71

1F4_5E2
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 285
SEQ ID NO. 288

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 286
SEQ ID NO. 289

HC CDR3
LC CDR3

SMVSSMDL
AAWDDSLSTHWV

SEQ ID NO. 287
SEQ ID NO. 290

1F4_5F2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSMRSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S
SEQ ID NO. 74

SEQ ID NO. 73

1F4 5F2
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 291
SEQ ID NO. 294

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 292
SEQ ID NO. 295

HC CDR3
LC CDR3

SMRSSMDL
AAWDDSLSAHWV

SEQ ID NO. 293
SEQ ID NO. 296

LN-97S
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S

SEQ ID NO. 297
SEQ ID NO. 298

LN-97S
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 299
SEQ ID NO. 302

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 300
SEQ ID NO. 303

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLSAHWV

SEQ ID NO. 301
SEQ ID NO. 304

Example 3. Specificity of Anti-KRAS Antibodies to Cellular Targets

Specificity of the anti-KRAS antibodies described in Tables 2 and 3 were tested for their specificity to human cells expressing wild type KRAS or mutant versions of KRAS associated with cancer. Specifically, binding of human anti-KRAS antibodies 1E3, 4F10, and LN97S to cellular targets in KRAS G12D over-expressing pancreatic tumor cells (ASPC-1), U2OS human osteosarcoma cells (KRAS wildtype), and A549 human lung adenocarcinoma epithelial cells (KRASG12S expressing cells) was tested. The G12S mutation results in an amino acid substitution at position 12 in KRAS, from a glycine (G) to a serine (S). The G12 D mutation results in in an amino acid substitution at position 12 in KRAS, from a glycine (G) to an aspartic acid (D).

Binding of anti-KRAS antibodies to cellular human KRAS proteins was measured by high content screening (HCS) microscopic assay. Briefly, cells were seeded in complete media (10% FBS DMEM, F12-K, RPMI, DMEM respectively) overnight in a black-walled 96-well plate. The next day, the antibody clones were added to the permeabilized cells and incubated overnight. Goat anti-Human IgG conjugated to Alexa488 (green fluorophore) was then added to the wells. Green signals were visualized by HCS confocal microscopy, then the cumulative mean fluorescence intensity was analyzed by ImageXpress software.

The results of the study are shown in FIG. 1, where binding of the antibody is shown as fold change relative to wild type. Anti-KRAS antibodies 1E3, 4F10 and LN97S showed enhanced binding to cellular proteins in KRAS G12D-overexpressing pancreatic tumor cells. LN97S also showed enhanced binding to KRAS G12S-overexpressing cells.

Example 4. Selection of Anti-KRAS G12D Antibody 4F10

In vitro affinity maturation of antibody 1F4 was carried out to increase antibody affinity to antigen and functional activity, as described in Example 2. Antibody 1F4 is specific for KRAS G12D. After screening for antibodies that showed improved binding affinity to recombinant proteins as well as cellular targets compared to parental antibody clone 1F4, anti-KRAS G12D antibody 4F10 was selected for further functionality evaluation. The additional experiments are described below in Examples 5-9, including anti-KRAS G12D antibody or KRAS G12D iTAbs comprising the 4F10 antibody. In the below examples, as controls fully human IgGs specific for bacterial proteins were produced and modified with the same procedure as KRAS iTAbs, then included as experimental control iTAbs. The sequences of antibody 4F10 are provided in SEQ ID Nos: 15 (heavy chain variable region), 16 (light chain variable region), 117-119 (CDRs of heavy chain variable region), and 120-122 (CDRs of light chain variable region).

Example 5. Anti-KRAS G12D Antibody Binding Activity to KRAS Proteins

The binding of anti-KRAS G12D antibody 4F10 to KRAS wild type and mutant proteins was determined using ELISA. An anti-h-Fc-HRP antibody was used as a control. Briefly, diluted anti-KRAS G12D clone 4F10 antibodies were incubated in a plate coated with recombinant human KRAS proteins. After incubation, a goat anti-human IgG Fc mAb conjugated to horse radish peroxidase (HRP) (secondary antibody) was added and bound to the Fc region of anti-KRAS mAbs. The Fc bound secondary antibodies were detected by addition of chromogen substrate. The color intensity developed was proportional to the amount of anti-KRAS antibody in the sample. A summary of the binding characteristics of 4F10 is provided in FIG. 3A, which provides results showing that antibody 4F10 preferentially bound to the mutant form of KRAS G12D and showed little to no binding to wild type or KRAS G12C.

HCS confocal microscopy was also used to measure 4F10 antibody binding to cellular proteins. Cells were seeded onto a collagen-coated 96-well plate overnight. The next day, cells were fixed, permeabilized, and blocked with ImagIT Image Enhancer for 30 minutes. Cells were stained with anti-KRAS antibodies overnight at 4° C. Cells were washed and incubated with anti-Human Alexa 488 and imaged using HCS confocal microscope. U2OS are osteosarcoma cells expressing wild-type KRAS. A549 are human lung cancer cells with KRAS G12S. ASPC-1 are human pancreatic cancer cells with KRAS G12D mutation. The results are described in FIG. 3B.

The results from FIG. 3A and FIG. 3B show that the anti-KRAS G12D 4F10 antibody binds selectively to KRAS G12D mutant proteins.

Example 6. Binding Activity of KRAS G12D 4F10 Antibody Conjugate

The binding activity of an anti-KRAS G12D 4F10 antibody conjugate (Compound 1) was examined Conjugated 4F10 was made according to the methods described herein. Briefly, diluted anti-KRAS G12D 4F10 antibody or conjugated 4F10 antibody (KRAS G12D iTAb (Compound 1)) were each incubated in a plate coated with recombinant human KRAS proteins. After incubation, goat anti-human IgG Fc mAb conjugated to horse radish peroxidase (HRP) (secondary antibody) was added and bound to the Fc region of anti-KRAS mAbs. The Fc bound secondary antibodies were detected by the addition of chromogen substrate. The color intensity developed was proportional to the amount of anti-KRAS mAb in the sample. FIG. 4 shows the results of these experiments, comparing the binding activity of the unconjugated anti-KRAS G12D 4F10 antibody and the anti-KRAS G12D 4F10 antibody conjugate (Compound 1) by ELISA. As shown in FIG. 4, modification (i.e., conjugation) of the anti-KRAS 4F10 antibody did not substantially affect the binding activity between the antibody and its antigen.

Example 7. KRAS G12D Antibody Conjugate Accumulation within Tumor Cells

Experiments were performed to examine the accumulation of the KRAS G12D 4F10 antibody conjugate (Compound 1) in tumor cells. Briefly, ASPC-1 human pancreatic tumor cells, which are positive for KRAS G12D, were incubated with the KRAS G12D clone 4F10 antibody conjugate (Compound 1). Nuclei were visualized by blue fluorescence, cell membrane was visualized by green fluorescence, and the antibody was visualized by red fluorescence. The KRAS G12D 4F10 antibody conjugate (Compound 1) was able to internalize into KRAS G12D expressing cancer cells (ASPC-1), seen by red colored antibodies inside the identifiable cell boundaries stained with WGA (wheat germ agglutinin; green) (data not shown).

Example 8. Internalized Anti-KRAS G12D Antibody Conjugates Attenuate Oncogenic Signaling in Human Pancreatic Cancer Cells Expressing KRAS G12D

The effect of internalized anti-KRAS G12D antibodies on oncogenic signaling was examined in ASPC-1 human pancreatic cancer cells expressing KRAS G12D. U2OS osteosarcoma cells expressing wild-type KRAS were used as a control. FIG. 5A shows the level of ERK 1/2 phosphorylation in U2OS KRAS wild type cells, in U2OS KRAS wild type cells stimulated with EGF, and in ASPC-1 cells with a KRAS G12D mutation after treatment with a control antibody conjugates (Control iTAbs) or treatment with anti-KRAS G12D clone 4F10 antibody conjugates (KRAS G12D iTAb (Compound 1)). As shown in FIG. 5A, the anti-KRAS G12D clone 4F10 antibody conjugates (Compound 1) inhibited level of ERK 1/2 phosphorylation. FIG. 5B shows the percent viability of the KRAS G12D cells after treatment with the control antibody conjugates (Control iTAbs) or the anti-KRAS G12D clone 4F10 antibody conjugates (KRAS G12D iTAb (Compound 1)). FIG. 5B shows that the anti-KRAS G12D clone 4F10 antibody conjugates decrease cell viability.

Example 9. Drug Sensitivity to KRAS G12D Antibody Conjugate in a 2D Tumor Growth Assay

The drug sensitivity to KRAS G12D 4F10 antibody conjugate (Compound 1) was tested in a 2-dimensional tumor growth assay in U2OS osteosarcoma cells expressing wild-type KRAS (a control) and ASPC-1 human pancreatic cancer cells expressing the KRAS G12D mutation. Control antibody conjugate (Control iTAb), anti-KRAS G12D 4F10 monoclonal antibody (KRAS^G12DmAb) and anti-KRAS G12D 4F10 antibody conjugate (KRAS^G12DiTAb (Compound 1)) were each tested for their effect on U2OS and ASPC-1 cells. A CellTiter-Glo (CTG) assay was performed to determine cell viability. The results are shown in FIG. 6A for U2OS KRAS wild type cells and in FIG. 6B for ASPC-1 KRAS G12D expressing human pancreatic cancer cells. As shown in FIG. 6A and FIG. 6B, anti-KRAS G12D 4F10 antibody conjugates (Compound 1) showed cytotoxic activity in ASPC-1 cells, but not U2OS cells.

TABLE 4

Antibody Amino Acid Sequences

Heavy chain
Light chain

variable domain regions
variable domain regions

K3-1F4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSLNAHWVFGGGTKLTVL

S
SEQ ID NO. 2

SEQ ID NO. 1

K3-1F4
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 75
SEQ ID NO. 78

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 76
SEQ ID NO. 79

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLNAHWV

SEQ ID NO. 77
SEQ ID NO. 80

K3-1A7
QVQLVESGGGVVQPGRSLRLSCTNSGFSF
DIVMTQSPSTLSASVGDRVTITCRASQSI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

SSWLAWYQQKPGKAPKVLIYKASSLESGV

YYADSVKGRFTISRDNSKNTLYLHMNSLR
PSRFSGSGSGTEFTLTISSLQPDDFAAYY

AEDTAVYYCASGGNYYGSGTIVSHGLDFW
CQHYNSYPYTFGQGTKLEIK

GQGTTVTVSS
SEQ ID NO. 4

SEQ ID NO. 3

K3-1A7
HC CDR1
LC CDR1

GFSFSGYAMH
RASQSISSWLA

SEQ ID NO. 81
SEQ ID NO. 84

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
KASSLES

SEQ ID NO. 82
SEQ ID NO. 85

HC CDR3
LC CDR3

GGNYYGSGTIVSHGLDF
QHYNSYPYT

SEQ ID NO. 83
SEQ ID NO. 86

K3-2B2
QVQLVESGGGVVQPGRSLRLSCTNSGFSF
SSELTQDPAVSVALGQTVRITCQGDSLRS

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

YYASWYQQKPGQAPVLVIYGKNNRPSGIP

YYADSVKGRFTISRDNSKNTLYLHMNSLR
DRFSGSSSGNTASLTITGAQAEDEADYYC

AEDTAVYYCASGGNYYGSGTIVSHGMDVW

NSRDSSGNHRGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 6

SEQ ID NO. 5

K3-2B2
HC CDR1
LC CDR1

GFSFSGYAMH
QGDSLRSYYAS

SEQ ID NO. 87
SEQ ID NO. 90

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
GKNNRPS

SEQ ID NO. 88
SEQ ID NO. 91

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
NSRDSSGNH

SEQ ID NO. 89
SEQ ID NO. 92

K3-2C2
QVQLVESGGGVVQPGRSLRLSCSNSGFSF
DIVMTQSPSSLSASVGDRVTITCRASQSI

SGYTMHWVRQAPGKGLEWVAVISFDGSHK

SNYLNWYQQKPGKAPKLLIYAASSLQSGV

YYADSVKGRFTISRDNSKNTLYLHMNSLR
PSRFSGSGSGTDFTLTISSLQPEDFATYY

AEDTAVYYCAKKMHYGSGAYHFDLWGQGT
CQQSYSSPFTFGPGTKVDIK

LVTVSS
SEQ ID NO. 8

SEQ ID NO. 7

K3-2C2
HC CDR1
LC CDR1

GFSFSGYTMH
RASQSISNYLN

SEQ ID NO. 93
SEQ ID NO. 96

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
AASSLQS

SEQ ID NO. 94
SEQ ID NO. 97

HC CDR3
LC CDR3

KMHYGSGAYHFDL
QQSYSSPFT

SEQ ID NO. 95
SEQ ID NO. 98

K3-2H8
EVQLLESGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYNYVSWYQQHPGKAPKLMIYDVSNRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLT
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTSSSTLVVFGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 10

SEQ ID NO. 9

K3-2H8
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDVGGYNYVS

SEQ ID NO. 99
SEQ ID NO. 102

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSNRPS

SEQ ID NO. 100
SEQ ID NO. 103

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTSSSTLVV

SEQ ID NO. 101
SEQ ID NO. 104

K3-3E8
EVQLLEPGGGVVQPGRSLRLSCTNSGFSF
QSALTQPRSVSGSPGQSVTISCTGTSSNV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYNHVSWYQQHPGKAPKVIIYDVNKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLR
GVSHRFSGSKSANTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTTSSTYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 12

SEQ ID NO. 11

K3-3E8
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSNVGGYNHVS

SEQ ID NO. 105
SEQ ID NO. 108

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVNKRPS

SEQ ID NO. 106
SEQ ID NO. 109

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTTSSTYV

SEQ ID NO. 107
SEQ ID NO. 110

K3-4D9
QVQLVESAGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDV

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGYKYVSWYQQYPGKAPKLMIYDVSKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLT
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCNSYTSSRIYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 14

SEQ ID NO. 13

K3-4D9
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDVGGYKYVS

SEQ ID NO. 111
SEQ ID NO. 114

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSKRPS

SEQ ID NO. 112
SEQ ID NO. 115

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
NSYTSSRIYV

SEQ ID NO. 113
SEQ ID NO. 116

K3-4F10
EVQLLEPGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSNDI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GAYNYVSWYQQHPGKAPKLMIYDVNNRPS

YYADSVKGRFTISRDNSKNTLYLHMNSLR
GVPDRFSGSKSGNMASLTISGLQAEDDAD

AEDTAVYYCASGGNYYGSGTIVSHGMDVW
YYCSSYTSSSTLVVFGGGTKLTVL

GQGTTVTVSS
SEQ ID NO. 16

SEQ ID NO. 15

K3-4F10
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSNDIGAYNYVS

SEQ ID NO. 117
SEQ ID NO. 120

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVNNRPS

SEQ ID NO. 118
SEQ ID NO. 121

HC CDR3
LC CDR3

GGNYYGSGTIVSHGMDV
SSYTSSSTLVV

SEQ ID NO. 119
SEQ ID NO. 122

K3-5H6
QVQLVQSGGGVVQPGRSLRLSCTNSGFSF
QSVLTQPASVSGSPGQSITISCTGTSSDI

SGYAMHWVRQAPGKGLEWVAVISFDGSHK

GGSNWVSWYQQHPGKAPKLMIYDVSKRPS

YYADSVKGRFTISRDNSKNTLYLHMNSVR
GVSNRFSGSKSGNTASLTISGLQAEDEAD

AEDTAVYYCASGGNHYGSGTIVSHGMDVR
YYCSSYTSSSTYVFGTGTKLTVL

GQGTTVTVSS
SEQ ID NO. 18

SEQ ID NO. 17

K3-5H6
HC CDR1
LC CDR1

GFSFSGYAMH
TGTSSDIGGSNWVS

SEQ ID NO. 123
SEQ ID NO. 126

HC CDR2
LC CDR2

VISFDGSHKYYADSVKG
DVSKRPS

SEQ ID NO. 124
SEQ ID NO. 127

HC CDR3
LC CDR3

GGNHYGSGTIVSHGMDV
SSYTSSSTYV

SEQ ID NO. 125
SEQ ID NO. 128

K5-1F12
QVQLVESGGGLVQPGGSLRLSCAASGFTF
QAGLTQPASVSGSPGQSITISCTGTSSDV

SSYWMSWVRQAPGKGLEWVGFIRSKAYGG

GGYNYVSWYQQHPGKAPKLMIYDVSKRPS

TTEYAASVKGRFTISRDDSKSIAYLQMNS
GVSNRFSGSKSGNTASLTISGLQAEDEAD

LKTEDTAVYYCTRDGGSYFDYWGQGTLVT
YYCSSYTSSSTYVFGTGTKVTVL

VSS
SEQ ID NO. 20

SEQ ID NO. 19

K5-1F12
HC CDR1
LC CDR1

GFTFSSYWMS
TGTSSDVGGYNYVS

SEQ ID NO. 129
SEQ ID NO. 132

HC CDR2
LC CDR2

FIRSKAYGGTTEYAASVKG
DVSKRPS

SEQ ID NO. 130
SEQ ID NO. 133

HC CDR3
LC CDR3

DGGSYFDY
SSYTSSSTYV

SEQ ID NO. 131
SEQ ID NO. 134

1F4_1H2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SLNGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYGSTHWVFGGGTKLTVL

S
SEQ ID NO. 22

SEQ ID NO. 21

1F4_1H2
HC CDR1
LC CDR1

GFTSSLNGMH
SGSNSNIGKNYVS

SEQ ID NO. 135
SEQ ID NO. 138

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 136
SEQ ID NO. 139

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYGSTHWV

SEQ ID NO. 137
SEQ ID NO. 140

1F4_1C3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RQYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDGRKVHWVFGGGTKLTVL

S
SEQ ID NO. 24

SEQ ID NO. 23

1F4_1C3
HC CDR1
LC CDR1

GFTSRQYGMH
SGSNSNIGKNYVS

SEQ ID NO. 141
SEQ ID NO. 144

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 142
SEQ ID NO. 145

HC CDR3
LC CDR3

SLYSSMDL
AAWDDGRKVHWV

SEQ ID NO. 143
SEQ ID NO. 146

1F4_1D3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

STYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSRTTHWVFGGGTKLTVL

S
SEQ ID NO. 26

SEQ ID NO. 25

1F4_1D3
HC CDR1
LC CDR1

GFTSSTYGMH
SGSNSNIGKNYVS

SEQ ID NO. 147
SEQ ID NO. 150

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 148
SEQ ID NO. 151

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSRTTHWV

SEQ ID NO. 149
SEQ ID NO. 152

1F4_1E6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RPYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDFHSEHWVFGGGTKLTVL

S
SEQ ID NO. 28

SEQ ID NO. 27

1F4_1E6
HC CDR1
LC CDR1

GFTSRPYGMH
SGSNSNIGKNYVS

SEQ ID NO. 153
SEQ ID NO. 156

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 154
SEQ ID NO. 157

HC CDR3
LC CDR3

SLYSSMDL
AAWDDFHSEHWV

SEQ ID NO. 155
SEQ ID NO. 158

1F4_1F6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

ATYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSSDTHWVFGGGTKLTVL

S
SEQ ID NO. 30

SEQ ID NO. 29

1F4_1F6
HC CDR1
LC CDR1

GFTSATYGMH
SGSNSNIGKNYVS

SEQ ID NO. 159
SEQ ID NO. 162

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 160
SEQ ID NO. 163

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSSDTHWV

SEQ ID NO. 161
SEQ ID NO. 164

1F4_1G6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SFHGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSGDVHWVFGGGTKLTVL

S
SEQ ID NO. 32

SEQ ID NO. 31

1F4_1G6
HC CDR1
LC CDR1

GFTSSFHGMH
SGSNSNIGKNYVS

SEQ ID NO. 165
SEQ ID NO. 168

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 166
SEQ ID NO. 169

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSGDVHWV

SEQ ID NO. 167
SEQ ID NO. 170

1F4_1E3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYRGPHWVFGGGTKLTVL

S
SEQ ID NO. 34

SEQ ID NO. 33

1F4_1E3
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 171
SEQ ID NO. 174

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 172
SEQ ID NO. 175

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYRGPHWV

SEQ ID NO. 173
SEQ ID NO. 176

1F4_3D11
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYRGPHWVFGGGTKLTVL

S
SEQ ID NO. 36

SEQ ID NO. 35

1F4_3D11
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 177
SEQ ID NO. 180

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 178
SEQ ID NO. 181

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYRGPHWV

SEQ ID NO. 179
SEQ ID NO. 182

1F4_4E10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RAPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDHNGEHWVFGGGTKLTVL

S
SEQ ID NO. 38

SEQ ID NO. 37

1F4_4E10
HC CDR1
LC CDR1

GFTSRAPGMH
SGSNSNIGKNYVS

SEQ ID NO. 183
SEQ ID NO. 186

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 184
SEQ ID NO. 187

HC CDR3
LC CDR3

SLYSSMDL
AAWDDHNGEHWV

SEQ ID NO. 185
SEQ ID NO. 188

1F4_4F10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDKFGVHWVFGGGTKLTVL

S
SEQ ID NO. 40

SEQ ID NO. 39

1F4_4F10
HC CDR1
LC CDR1

GFTSRHPGMH
SGSNSNIGKNYVS

SEQ ID NO. 189
SEQ ID NO. 192

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 190
SEQ ID NO. 193

HC CDR3
LC CDR3

SLYSSMDL
AAWDDKFGVHWV

SEQ ID NO. 191
SEQ ID NO. 194

1F4_4A12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSPTIHWVFGGGTKLTVL

S
SEQ ID NO. 42

SEQ ID NO. 41

1F4_4A12
HC CDR1
LC CDR1

GFTSRKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 195
SEQ ID NO. 198

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 196
SEQ ID NO. 199

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSPTIHWV

SEQ ID NO. 197
SEQ ID NO. 200

1F4_4D12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNFNI

HNKGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDFAGVHWVFGGGTKLTVL

S
SEQ ID NO. 44

SEQ ID NO. 43

1F4_4D12
HC CDR1
LC CDR1

GFTSHNKGMH
SGSNFNIGKNYVS

SEQ ID NO. 201
SEQ ID NO. 204

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 202
SEQ ID NO. 205

HC CDR3
LC CDR3

SLYSSMDL
AAWDDFAGVHWV

SEQ ID NO. 203
SEQ ID NO.206

1F4_4E12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

YKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCASSLYSSMDLWGQGTTVTVS
YCAAWDDSFSEHWVFGGGTKLTVL

S
SEQ ID NO. 46

SEQ ID NO. 45

1F4_4E12
HC CDR1
LC CDR1

GFTSYKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 207
SEQ ID NO. 210

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 208
SEQ ID NO. 211

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSFSEHWV

SEQ ID NO. 209
SEQ ID NO. 212

1F4_5C4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RAPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDQNGVHWVFGGGTKLTVL

S
SEQ ID NO. 48

SEQ ID NO. 47

1F4_5C4
HC CDR1
LC CDR1

GFTSRAPGMH
SGSNSNIGKNYVS

SEQ ID NO. 213
SEQ ID NO. 216

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 214
SEQ ID NO. 217

HC CDR3
LC CDR3

SLYSSMDL
AAWDDQNGVHWV

SEQ ID NO. 215
SEQ ID NO. 218

1F4_5A4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RSPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLRGVHWVFGGGTKLTVL

S
SEQ ID NO. 50

SEQ ID NO. 49

1F4_5A4
HC CDR1
LC CDR1

GFTSRSPGMH
SGSNSNIGKNYVS

SEQ ID NO. 219
SEQ ID NO. 222

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 220
SEQ ID NO. 223

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLRGVHWV

SEQ ID NO. 221
SEQ ID NO. 224

1F4_5B7
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RHHGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDRHGTHWVFGGGTKLTVL

S
SEQ ID NO. 52

SEQ ID NO. 51

1F4_5B7
HC CDR1
LC CDR1

GFTSRHHGMH
SGSNSNIGKNYVS

SEQ ID NO. 225
SEQ ID NO. 228

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 226
SEQ ID NO. 229

HC CDR3
LC CDR3

SLYSSMDL
AAWDDRHGTHWV

SEQ ID NO.227
SEQ ID NO. 230

1F4_5F8
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RNPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSTGVHWVFGGGTKLTVL

S
SEQ ID NO. 54

SEQ ID NO. 53

1F4_5F8
HC CDR1
LC CDR1

GFTSRNPGMH
SGSNSNIGKNYVS

SEQ ID NO. 231
SEQ ID NO. 234

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 232
SEQ ID NO. 235

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSTGVHWV

SEQ ID NO. 233
SEQ ID NO. 236

1F4_5D3
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RTYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLPTDHWVFGGGTKLTVL

S
SEQ ID NO. 56

SEQ ID NO. 55

1F4_5D3
HC CDR1
LC CDR1

GFTSRTYGMH
SGSNSNIGKNYVS

SEQ ID NO. 237
SEQ ID NO. 240

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 238
SEQ ID NO. 241

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLPTDHWV

SEQ ID NO. 239
SEQ ID NO. 242

1F4_5G5
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

RQYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDYSGVHWVFGGGTKLTVL

S
SEQ ID NO. 58

SEQ ID NO. 57

1F4_5G5
HC CDR1
LC CDR1

GFTSRQYGMH
SGSNSNIGKNYVS

SEQ ID NO. 243
SEQ ID NO. 246

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 244
SEQ ID NO. 247

HC CDR3
LC CDR3

SLYSSMDL
AAWDDYSGVHWV

SEQ ID NO. 245
SEQ ID NO. 248

1F4_5A10
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SPYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDNPRDHWVFGGGTKLTVL

S
SEQ ID NO. 60

SEQ ID NO. 59

1F4_5A10
HC CDR1
LC CDR1

GFTSSPYGMH
SGSNSNIGKNYVS

SEQ ID NO. 249
SEQ ID NO. 252

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 250
SEQ ID NO. 253

HC CDR3
LC CDR3

SLYSSMDL
AAWDDNPRDHWV

SEQ ID NO. 251
SEQ ID NO. 254

1F4_5B12
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SKPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLRGVHWVFGGGTKLTVL

S
SEQ ID NO. 62

SEQ ID NO. 61

1F4_5B12
HC CDR1
LC CDR1

GFTSSKPGMH
SGSNSNIGKNYVS

SEQ ID NO. 255
SEQ ID NO. 258

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 256
SEQ ID NO. 259

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLRGVHWV

SEQ ID NO. 257
SEQ ID NO. 260

1F4_5C5
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

KKYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDLGGDHWVFGGGTKLTVL

S
SEQ ID NO. 64

SEQ ID NO. 63

1F4_5C5
HC CDR1
LC CDR1

GFTSKKYGMH
SGSNSNIGKNYVS

SEQ ID NO. 261
SEQ ID NO. 264

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 262
SEQ ID NO. 265

HC CDR3
LC CDR3

SLYSSMDL
AAWDDLGGDHWV

SEQ ID NO. 263
SEQ ID NO. 266

1F4_5F6
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

TLPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSAGVHWVFGGGTKLTVL

S
SEQ ID NO. 66

SEQ ID NO. 65

1F4_5F6
HC CDR1
LC CDR1

GFTSTLPGMH
SGSNSNIGKNYVS

SEQ ID NO. 267
SEQ ID NO. 270

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 268
SEQ ID NO. 271

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSAGVHWV

SEQ ID NO. 269
SEQ ID NO. 272

1F4_5H4
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

KMPGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDEHGVHWVFGGGTKLTVL

S
SEQ ID NO. 68

SEQ ID NO. 67

1F4_5H4
HC CDR1
LC CDR1

GFTSKMPGMH
SGSNSNIGKNYVS

SEQ ID NO. 273
SEQ ID NO. 276

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 274
SEQ ID NO. 277

HC CDR3
LC CDR3

SLYSSMDL
AAWDDEHGVHWV

SEQ ID NO. 275
SEQ ID NO. 278

1F4_5H1
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCAASLYSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S
SEQ ID NO. 70

SEQ ID NO. 69

1F4_5H1
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 279
SEQ ID NO. 282

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 280
SEQ ID NO. 283

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLSAHWV

SEQ ID NO. 281
SEQ ID NO. 284

1F4_5E2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSMVSSMDLWGQGTTVTVS
YCAAWDDSLSTHWVFGGGTKLTVL

S
SEQ ID NO. 72

SEQ ID NO. 71

1F4_5E2
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 285
SEQ ID NO. 288

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 286
SEQ ID NO. 289

HC CDR3
LC CDR3

SMVSSMDL
AAWDDSLSTHWV

SEQ ID NO. 287
SEQ ID NO. 290

1F4_5F2
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSMRSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S
SEQ ID NO. 74

SEQ ID NO. 73

1F4_5F2
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 291
SEQ ID NO. 294

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 292
SEQ ID NO. 295

HC CDR3
LC CDR3

SMRSSMDL
AAWDDSLSAHWV

SEQ ID NO. 293
SEQ ID NO. 296

LN-97S
EVQLVQSGGGVVQPGRSLRLSCAASGFTS
QSVVTQPPSVSAAPGQKVTISCSGSNSNI

SNYGMHWVRQAPGKGLEWVAVISHDGSKK

GKNYVSWFQQVPGTAPKLLIFEDNQRPSG

YYADSVKGRFTISRDNSKNTLFVQLSSLR
IPDRFSASKSGTSASLAISGLQSEDEADY

PEDTAVYYCATSLYSSMDLWGQGTTVTVS
YCAAWDDSLSAHWVFGGGTKLTVL

S
SEQ ID NO. 298

SEQ ID NO. 297

LN-97S
HC CDR1
LC CDR1

GFTSSNYGMH
SGSNSNIGKNYVS

SEQ ID NO. 299
SEQ ID NO. 302

HC CDR2
LC CDR2

VISHDGSKKYYADSVKG
EDNQRPS

SEQ ID NO. 300
SEQ ID NO. 303

HC CDR3
LC CDR3

SLYSSMDL
AAWDDSLSAHWV

SEQ ID NO. 301
SEQ ID NO. 304

Number	Name	Date	Kind
5977322	Marks et al.	Nov 1999	A
7498414	Zhu	Mar 2009	B2
7507797	Knackmuss et al.	Mar 2009	B2
8329178	Marasco et al.	Dec 2012	B2
20050215770	Bell et al.	Sep 2005	A1

Number	Date	Country
62407982	Oct 2016	US
62414196	Oct 2016	US
62416913	Nov 2016	US

	Number	Date	Country
Parent	PCT/IB2017/056334	Oct 2017	US
Child	16380121		US

Anti-KRAS binding proteins

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

Field of Search

CPC

International Classifications

Abstract

Description

Claims

CROSS REFERENCE TO RELATED APPLICATIONS

US Referenced Citations (5)

Foreign Referenced Citations (1)

Non-Patent Literature Citations (7)

Related Publications (1)

Provisional Applications (3)

Continuations (1)

Entry
Strome et al., The Oncologist, 2007; 12:1084-95 (Year: 2007).
Brand et al., Anticancer Res. 2006; 26:463-70 (Year: 2006).
UniProtKB Accession No. A0A0G2K3A6, Jul. 22, 2015 [online]. Retrieved from the Internet: https://www.uniprot.org/uniprot/A0A0G2K3A6.txt?version=1 amino acids 26-35.
UniProtKB Accession No. G6B0U4, Jan. 25, 2012 [online]. Retrieved from the internet: https://www.uniprot.org/uniprot/G8B0U4.txt?version=1 amino acids 367-374.
UniProtKB Accession No. A2N2W8, Feb. 20, 2007 [online]. Retrieved from the internet: https://www.uniprot.org/uniprot/A2N2W8.txt?version=1 amino acids 39-45.
Shin et al., “Antibody Targeting Intracellular Oncogenic Ras Mutants Exerts Anti-Tumour Effects After Systemic Administration”, Nature Communications 8:15090 (May 10, 2017), pp. 1-14.
International Search Report corresponding to International Patent Application No. PCT/IB2017/056334, dated May 31, 2018, 5 pages.